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Aldrich Organometallic, Inorganic, Silanes, Boranes, and Deuterated Compounds
Aldrich Organometallic, Inorganic, Silanes, Boranes, and Deuterated Compounds Library Listing – 1,523 spectra Subset of Aldrich FT-IR Library related to organometallic, inorganic, boron and deueterium compounds. The Aldrich Material-Specific FT-IR Library collection represents a wide variety of the Aldrich Handbook of Fine Chemicals' most common chemicals divided by similar functional groups. These spectra were assembled from the Aldrich Collections of FT-IR Spectra Editions I or II, and the data has been carefully examined and processed by Thermo Fisher Scientific. Aldrich Organometallic, Inorganic, Silanes, Boranes, and Deuterated Compounds Index Compound Name Index Compound Name 1066 ((R)-(+)-2,2'- 1193 (1,2- BIS(DIPHENYLPHOSPHINO)-1,1'- BIS(DIPHENYLPHOSPHINO)ETHAN BINAPH)(1,5-CYCLOOCTADIENE) E)TUNGSTEN TETRACARBONYL, 1068 ((R)-(+)-2,2'- 97% BIS(DIPHENYLPHOSPHINO)-1,1'- 1062 (1,3- BINAPHTHYL)PALLADIUM(II) CH BIS(DIPHENYLPHOSPHINO)PROPA 1067 ((S)-(-)-2,2'- NE)DICHLORONICKEL(II) BIS(DIPHENYLPHOSPHINO)-1,1'- 598 (1,3-DIOXAN-2- BINAPH)(1,5-CYCLOOCTADIENE) YLETHYNYL)TRIMETHYLSILANE, 1140 (+)-(S)-1-((R)-2- 96% (DIPHENYLPHOSPHINO)FERROCE 1063 (1,4- NYL)ETHYL METHYL ETHER, 98 BIS(DIPHENYLPHOSPHINO)BUTAN 1146 (+)-(S)-N,N-DIMETHYL-1-((R)-1',2- E)(1,5- BIS(DI- CYCLOOCTADIENE)RHODIUM(I) PHENYLPHOSPHINO)FERROCENY TET L)E 951 (1,5-CYCLOOCTADIENE)(2,4- 1142 (+)-(S)-N,N-DIMETHYL-1-((R)-2- PENTANEDIONATO)RHODIUM(I), (DIPHENYLPHOSPHINO)FERROCE 99% NYL)ETHYLAMIN 1033 (1,5- 407 (+)-3',5'-O-(1,1,3,3- CYCLOOCTADIENE)BIS(METHYLD TETRAISOPROPYL-1,3- IPHENYLPHOSPHINE)IRIDIUM(I) -
Chemical Chemical Hazard and Compatibility Information
Chemical Chemical Hazard and Compatibility Information Acetic Acid HAZARDS & STORAGE: Corrosive and combustible liquid. Serious health hazard. Reacts with oxidizing and alkali materials. Keep above freezing point (62 degrees F) to avoid rupture of carboys and glass containers.. INCOMPATIBILITIES: 2-amino-ethanol, Acetaldehyde, Acetic anhydride, Acids, Alcohol, Amines, 2-Amino-ethanol, Ammonia, Ammonium nitrate, 5-Azidotetrazole, Bases, Bromine pentafluoride, Caustics (strong), Chlorosulfonic acid, Chromic Acid, Chromium trioxide, Chlorine trifluoride, Ethylene imine, Ethylene glycol, Ethylene diamine, Hydrogen cyanide, Hydrogen peroxide, Hydrogen sulfide, Hydroxyl compounds, Ketones, Nitric Acid, Oleum, Oxidizers (strong), P(OCN)3, Perchloric acid, Permanganates, Peroxides, Phenols, Phosphorus isocyanate, Phosphorus trichloride, Potassium hydroxide, Potassium permanganate, Potassium-tert-butoxide, Sodium hydroxide, Sodium peroxide, Sulfuric acid, n-Xylene. Acetone HAZARDS & STORAGE: Store in a cool, dry, well ventilated place. INCOMPATIBILITIES: Acids, Bromine trifluoride, Bromine, Bromoform, Carbon, Chloroform, Chromium oxide, Chromium trioxide, Chromyl chloride, Dioxygen difluoride, Fluorine oxide, Hydrogen peroxide, 2-Methyl-1,2-butadiene, NaOBr, Nitric acid, Nitrosyl chloride, Nitrosyl perchlorate, Nitryl perchlorate, NOCl, Oxidizing materials, Permonosulfuric acid, Peroxomonosulfuric acid, Potassium-tert-butoxide, Sulfur dichloride, Sulfuric acid, thio-Diglycol, Thiotrithiazyl perchlorate, Trichloromelamine, 2,4,6-Trichloro-1,3,5-triazine -
While There Are Many Thousands of Different Chemical Compounds There
NAMING CHEMICAL COMPOUNDS & WRITING CHEMICAL FORMULAS While there are many thousands of different chemical compounds there is a very definite system of nomenclature whereby we can name or write chemical formulas for most compounds. We divide the compounds into two main types – binary compounds and ternary compounds. I. Binary Compounds All true binary compounds contain only two elements. The name of every binary compound ends with “ide.” Binary compounds come in three types. They are: Type I ………. the metal forms only one type of cation Type II ……… the metal forms two or more types of cations Type III …….. contains only nonmetals We will look at each type, one at a time. Type I Binary Compounds For Type I binary compounds the metal present can be found in either Group 1 or Group 2 on the periodic table. The naming system for this type of compound is quite simple and is found below. Rules for naming Type I binary compounds 1. The cation is always name first and the anion second. 2. A simple cation (obtained from a single atom) takes its name from the name of the element. 3. A simple anion (obtained from a single atom) is named by taking the first part of the element name (the root) and adding the letters “IDE.” 4. Write the name for the compound by combining the names of the ions. When naming Type I binary compounds: name of first element root + ide The root is merely an abbreviation for the name of the second element. The roots of the most commonly used elements are listed in the following table. -
BGA244 Binary Gas Analyzer User Manual
BGA244 Binary Gas Analyzer User Manual Revision 1.10 Certification Stanford Research Systems certifies that this product met its published specification at the time of shipment. Warranty This Stanford Research Systems product is warranted against defects in materials and workmanship for a period of one (1) year from the date of shipment. Service For warranty service or repair, this product must be returned to a Stanford Research Systems authorized service facility. Contact Stanford Research Systems or an authorized representative for a RMA (Return Material Authorization) Number before returning this product for repair. These are available at www.thinksrs.com under Support, Repair/Calibration. All users returning a BGA244 back to the factory for repair and/or service must submit a correctly completed “Declaration of Contamination of Equipment” form, available as part of the RMA process. The SRS personnel carrying out repair and service of the BGA244 must be informed of the condition of the components prior to any work being performed. Warning All returns to SRS must be free of harmful, corrosive, radioactive or toxic materials. Dedication In memory of Jim Williams, 1948 - 2011: Legendary Author and Analog Design Guru Information in this document is subject to change without notice. Copyright © Stanford Research Systems, Inc., 2016-2018. All rights reserved. Stanford Research Systems, Inc. 1290-C Reamwood Avenue Sunnyvale, California 94089 Phone: (408) 744-9040 Fax: (408) 744-9049 Email: [email protected] www.thinksrs.com Printed in the -
WO 2016/074683 Al 19 May 2016 (19.05.2016) W P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2016/074683 Al 19 May 2016 (19.05.2016) W P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every C12N 15/10 (2006.01) kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (21) International Application Number: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, PCT/DK20 15/050343 DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (22) International Filing Date: HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, 11 November 2015 ( 11. 1 1.2015) KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, (25) Filing Language: English PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, (26) Publication Language: English SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (30) Priority Data: PA 2014 00655 11 November 2014 ( 11. 1 1.2014) DK (84) Designated States (unless otherwise indicated, for every 62/077,933 11 November 2014 ( 11. 11.2014) US kind of regional protection available): ARIPO (BW, GH, 62/202,3 18 7 August 2015 (07.08.2015) US GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, (71) Applicant: LUNDORF PEDERSEN MATERIALS APS TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, [DK/DK]; Nordvej 16 B, Himmelev, DK-4000 Roskilde DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, (DK). -
A Study of the Addition Compounds of Titanium Tetrabromide and Titanium Tetraiodide with 1,4-Dioxane, Tetrahydrofuran, and Tetrahydrqpyran
A STUDY OF THE ADDITION COMPOUNDS OF TITANIUM TETRABROMIDE AND TITANIUM TETRAIODIDE WITH 1,4-DIOXANE, TETRAHYDROFURAN, AND TETRAHYDRQPYRAN DISSERTATION Presented in Partial Fulfillment of tha Requirements for the Degree Doctor of Philosphy in the Graduate School of The Ohio State University Robert Fredrick Rolsten, B.S. The Ohio State University 1955 Approved by: D r ACKNOWLEDGEMENTS The author wishes to express appreciation to Dr. Harry H. Sisler for his continued personal interest and guidance throughout the course of the investigation. Appreciation is also extended to Dr. Edward D. Loughran for his cooperation in the use of the infrared spectro photometer, to Dr. Preston M. Harris and Mr. Herbert W. Newkirk for contributing to the interpretation of the X-Ray data. The arrangement between Battelle Memorial Institute and the Graduate School of The Ohio State University with regard to tuition is gratefully acknowledged. I fully recognize the sacrifice my children have made in tolerating my necessary absence while attending school and which resulted in my failing of fatherly obligations. I sincerely hope the means has not destroyed the end. ii TABLE OF CONTENTS Page ACKNOWLEDGEMENTS ......................................... ...... ii LIST OF ILLUSTRATIONS .......................................... iv LIST OF TABIES ............................................. viii I. INTRODUCTION .................................. 1 II. HISTORICAL ............................................... 3 III. PREPARATION AND PURIFICATION OF REAGENTS ............... -
Itetall IC BROMIDES AS CATALYSTS in THE
QUANTITATIVE COMPARISON OF ;itETALL IC BROMIDES AS CATALYSTS IN THE FRIED.liL-CRAFTS KETONE SYNTHESIS i QUANTITATIVE COMPARISON OF MET ALLIC BROMIDES AS CATAL YSTS IN THE FRIEDEL-CRAFTS KETONE SYNTHESIS By Peter Taketoshi M,, ori Bachelor of .Arts Park College Parkville, Missouri 1945 Submitted to the Department of Chemistry Oklahoma Agricultural and Mechanical College In partial fulfillment of the r equirement for t he Degree of Master of Science 194'~ ii \ APPROVED BY: Chairman, Thesis Committee Head of the Department ~he~ ( ~uate~~ School 2174~10 iii ACKNOWLEDGEMENT The author wis hes to express his s i neere gr atitude to Dr . O. C. Dermer under whose guidance t his work has been accomplished . He also wi s hes to express hi s a ppreciation to the Chemi stry Department for t he s uppl y of chemicals used. iv TABLE OF CONTENTS "P age Introduction • • l Historical • • • • 2 Experimental • • • • 5 Procadure • • • • • • • • 9 Table of results . • • • • • • • 12 Discussion of results • .. • • • • • • 15 Summary • • • • • • • • 22 Bibliography • • • • • • • • • • 23 Biography • • • • • • • • • • • 25 1 I NTRODCCT ION T~lis is a continuation of the s t udy of catalystf for the Friedel Crafts ketone synt hesis star ted by Wilson ( .38 ), a nd continued by Suguj. tan (34), Johnson (17), and Billme ier (4). Ma ny metallic chlorides have been used in t his reacti on, but metallic bromides, as cat alyst s, have been rather neelected . It is the purpose of this work to study the ef fectiveness of some of the metallic bromides by following essentially the experimental pro cedure of Billmeier (4). 2 HISTORICAL In 1877, the French chemist Friedel and his American colleague Crafts (12) discovered the f amous Friedel-Crafts reaction, which now has s uch great industrial a pplication (7 , 13, 18, 35). -
WO 2013/089962 Al 20 June 2013 (20.06.2013) W P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2013/089962 Al 20 June 2013 (20.06.2013) W P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every B01J 31/04 (2006.01) B01J 31/18 (2006.01) kind of national protection available): AE, AG, AL, AM, B01J 31/14 (2006.01) B01J 31/22 (2006.01) AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, (21) Number: International Application DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, PCT/US20 12/065285 HN, HR, HU, ID, IL, IN, IS, JP, KE, KG, KM, KN, KP, (22) International Filing Date: KR, KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, 15 November 2012 (15.1 1.2012) ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, (25) Filing Language: English RW, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, (26) Publication Language: English TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (30) Priority Data: 13/323,328 12 December 201 1 (12. 12.201 1) US (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, (71) Applicant (for all designated States except US): CHEV¬ GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, SZ, TZ, RON PHILLIPS CHEMICAL COMPANY LP UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, [US/US]; 10001 Six Pines Drive, The Woodlands, Texas TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, 77380 (US). -
How to Use This Guide Dielectric Constant Table
Dielectric Constant Table.xls Dielectric Constant Table Dielectric Constant (k) is a number relating the ability of a material to carry alternating current to the ability of vacuum to carry alternating current. The capacitance created by the presence of the material is directly related to the Dielectric Constant of the material. Alphabetic Table A B C D Knowing the Dielectric Constant (k) of a material is needed to properly E F G H design and apply instruments such as level controls using radar, RF I J K L admittance, or capacitance technologies. There are also analytical M N O P reasons to know the (k) of a material. Q R S T U V W X How to use this guide Y Z # CLIPPER CONTROLS has compiled an extensive list of products with Dielectric Constants. Many of these Dielectric Constants are given at specific temperatures. If your product's temperature is significantly different from those listed there is a good chance that the Dielectric Constant may be different from the values listed. The products in this reference are listed in alphabetical order and are grouped in sections by the first letter of their name. Proper chemical names were used, and any trade names are the trademark of their respective owners. If you know the correct spelling of the name of the product you wish to review then use the "Search" feature on the web browser to locate the name in the list. You may also click on the letter from the alphabetical table to go directly to the beginning of that alphabetic section. -
United States Patent Office Patented Dec
3,481,871 United States Patent Office Patented Dec. 2, 1969 1. 3,481,871 DTHOETHANE, DERVATIVES AND ORGANIC COMPOSTIONS CONTAINING THE SAME Herbert Myers, Barrington, and Alfred P. Kozacik, Woodbury, N.J., assignors to Mobil Oil Corpo ration, a corporation of New York No Drawing. Filed Apr. 24, 1967, Ser. No. 632,907 Int. CI. C10m 1/38, 3/32; C07c. 149/12 U.S. C. 252-45 2 Claims O and ABSTRACT OF THE DISCLOSURE Novel organo-sulfur derivatives are produced by re acting a mercaptain with a sulfur chloride compound, reacting the resulting organic sulfenyl or thiosulfenyl 5 chloride with an olefin, and finally reacting the resulting SSR, product with a metal sulfur-containing salt. The final product may be used in lubricating oils and other in wherein R, R2, and x have the above definitions, and X dustrial fluids as a load-carrying additive. is oxygen or sulfur, Y is oxygen, sulfur or nitrogen and 20 R is hydrogen, or alkyl, cycloalkyl, aralkyl, aryl or alkaryl having from 1 to 20 carbon atoms. Rb may also FIELD OF INVENTION contain nitrogen, oxygen- or sulfur-containing Substi This invention relates to organic compositions con tletS. taining novel organo-sulfur derivatives of dithioethanes, and to a method of producing these derivatives. 25 DESCRIPTION OF SPECIFIC EMBODIMENTS PRIOR ART The products of this invention are produced by react In U.S. Patents Nos. 2,708,199 and 2,886,593, specific ing (1) a mercaptan, RSH, with (2) a sulfur halide. The sulfur compounds have been disclosed. In the first-named resulting organosulfenyl halide is then reacted with (3) patent, there is disclosed a method of producing organic 3) an olefin, CRR2=CHP, to produce an organo thioethyl polysulfides by reacting an olefin having from 6 to 30 halide intermediate. -
Studies on the Use of Supercritical Ammonia for Ceramic Nitride Synthesis and Fabrication
NASA Technical Memorandum 102570 Studies on the Use of Supercritical Ammonia for Ceramic Nitride Synthesis and Fabrication Linda Cornell and Y.C. Lin Case Western Reserve University Cleveland, Ohio Warren H. Philipp Lewis Research Center Cleveland, Ohio April 1990 (_A5 A- l'M-3 025-rt)) 5T_Jr_i r 3 .JU F, -r_,C C, II-ICAL Am_C_NIA r:_n_ C F¢A,'4 IC NIl_ Ir'__ SYNTH=_I$ A_I_; FAjR_ICATI_N CSCt 0 l_ G3125 STUDIES ON THE USE OF SUPERCRITICAL AMMONIA FOR CERAMIC NITRIDE SYNTHESIS AND FABRICATION Linda Cornell* and Y.C. Lin* Case Western Reserve Unlversity Cleveland, Ohio 44106 and Warren H. Phillpp National Aeronautics and Space Administration Lewis Research Center Cleveland, Ohio 44135 ABSTRACT The extractablIity of ammonium halldes (Including ammonium thiocyanate) formed as byproducts from the synthesis of Si(NH) 2 via ammonolysis of the cor- respondlng sillcon tetrahalldes using supercritical NH 3 as the extraction medium has been investigated. It was found that the NH4SCN byproduct of ammo- noIysls of SI(SCN) 4 can be almost completely extracted with SC ammonia from the insoluble SI(NH) 2 forming a promlslng system for the synthesis of pure Si(NH) 2, one of the best precursors to SI3N 4. In addltion, it was found that Si3N 4, AIN, BN, and Si(NH) 2 are insoluble in SC ammonla. Also discussed are design consideratlons for a supercritical ammonia extraction unit. INTRODUCTION Supercritical flulds (fluids above their crltical temperature and pres- sure) are used as solvents and extraction media because of their near zero sur- face tension and good solvent properties. -
(10) Patent No.: US 7759518 B2
USOO7759518B2 (12) United States Patent (10) Patent No.: US 7,759,518 B2 Maderna et al. (45) Date of Patent: *Jul. 20, 2010 (54) DERIVATIVES OF N-(ARYLAMINO) 2004/0171632 A1 9, 2004 Gowan et al. SULFONAMIDESAS INHIBITORS OF MEK 2004/0176418 A1 9/2004 Thiruvengadam et al. 2005, 0004186 A1 1/2005 Barrett et al. (75) Inventors: Andreas Maderna, Stony Point, NY a a (US); Jean-Michel Vernier, San Diego 2005/002697O A1 2/2005 Barrett et al. CA (US). Dinesh Barawkar Foothill s 2005.0054701 A1 3/2005 Wallace et al. Ranch, CA (US), Varaprasad 2006/003061.0 A1 2/2006 Koch et al. Chamakura, Bangalore (IN); Hassan el 2006, O140872 A1 6/2006 Furue et al. Abdellaoui, Jamestown, NC (US); Zhi 2008/005834.0 A1 3/2008 Madeirna et al. Hong, Irvine, CA (US) (73) Assignee: Ardea Biosciences, San Diego, CA (US) FOREIGN PATENT DOCUMENTS (*) Notice: Subject to any disclaimer, the term of this patent is extended or adjusted under 35 EP 239362 A2 9, 1987 U.S.C. 154(b) by 0 days. EP 606046 T 1994 This patent is Subject to a terminal dis- EP T80386 6, 1997 claimer. EP O818.442 A2 1, 1998 EP 93.1788 A2 7, 1999 (21) Appl. No.: 12/323,279 EP O945864 A2 9, 1999 EP 1004578 A2 5, 2000 (22) Filed: Nov. 25, 2008 WO WO-90-05719 A1 5, 1990 (65) Prior Publication Data WO WO-96-27583 A1 3, 1996 WO WO-96-33182 A1 10, 1996 US 2009/OO82457 A1 Mar. 26, 2009 WO WO-98-07697 A1 2/1998 Related U.S.