On Semiconductor Corp Semiconductors and Related Devices
5005 E Mcdowell Rd # A202, Phoenix, AZ 85008
Jeffrey Robbins Senior Air Quality Chemist
Bay Area Air Quality Management District Air and Water Resource and Solid Waste Manage...
939 Ellis St, San Francisco, CA 94109
Jeffrey Robbins Vice-president
PLAZA RESEARCH CORPORATION
2338 W Royal Palm Rd STE -J, Phoenix, AZ 85021 120 Rte 17 N, Paramus, NJ 07652
Jeffrey R. Robbins President, Principal
DECONFUSION CONSULTING CORPORATION Business Consulting Services
PO Box 6104, Moraga, CA 94570 Moraga, CA 94570 143 Dearflag Rd, Schellville, CA 95476
Jeffrey Robbins Senior Air Quality Chemist
Bay Area Air Quality Management District Administration of Air and Water Resource and Solid Waste Man
939 Ellis St, San Francisco, CA 94109 4157495000, 4157495111, 4157495189, 4157714932
Jeffrey Robbins Director, Vice President
PLAZA RESEARCH CORPORATION Commercial Nonphysical Research · Market Research · Nonclassifiable Establishments
120 N State Rt 17 STE 201, Paramus, NJ 07652 Paramus, NJ 07652 4000 Hollywood Blvd, Hollywood, FL 33021 55 Stockton St STE 400, San Francisco, CA 94108 2012657500, 4159840400, 9549637600, 9549874734
Jeffrey Robbins Manager
ON Semiconductor Semiconductors · Mfg Semiconductors/Devices Electric Measuring Instrument & Home Audio/Video Equipment · Mfg Semiconductors/Dvcs Engineering Services Elec Measuring Instr & Home Audio/Video Eqp · Mfg Semiconductors/Dvcselec Measuring Instr & Home Audio/Video Eqp · Nonclassifiable Establishments · Semiconductors and Related Devices · Semiconductor Devices (Manufac
5005 E Mcdowell Rd, Phoenix, AZ 85008 5005 E Mcdowell Rd Ms C 250, Phoenix, AZ 85008 1209 Orange St, Wilmington, DE 19801 6022446600, 6022446071, 6022447160, 6022447005
Dr. Robbins graduated from the St. George's University School of Medicine, St. George's, Greneda in 1983. He works in Avon, CT and 1 other location and specializes in Internal Medicine - Geriatrics and Internal Medicine.
Primary HealthPrimary Health Medical Group 4815 Cleveland Blvd, Caldwell, ID 83605 2084553545 (phone), 2084549690 (fax)
Languages:
English Spanish
Description:
Mr. Robbins works in Caldwell, ID and specializes in Family Medicine. Mr. Robbins is affiliated with St Lukes Meridian Medical Center and West Valley Medical Center.
Louis Stokes VA Medical Center Podiatry 10701 East Blvd #112W, Cleveland, OH 44106 2162313286 (phone), 2162313446 (fax)
Languages:
English
Description:
Dr. Robbins works in Cleveland, OH and specializes in Podiatric Medicine. Dr. Robbins is affiliated with Cleveland Clinic, Louis Stokes VA Medical Center, University Hospital Ahuja Medical Center and University Hospitals Cleveland Medical Center.
Jeffrey D. Robbins - Berkeley CA Richard D. Gless - Oakland CA
Assignee:
ICI Americas Inc. - Wilmington DE
International Classification:
C07F 940
US Classification:
558 98
Abstract:
Thiophosphonate compounds having the formula ##STR1## in which R is alkyl, haloalkyl or aryl; X is chloro or SR. sub. 2 ; R. sub. 1 is alkyl or aryl; and when X is SR. sub. 2 then R. sub. 2 is a group identical to R. sub. 1, or R. sub. 1 and R. sub. 2 taken together form an optionally alkyl-substituted polymethylene group, are prepared by reaction of a thiophosphonodichloride with a mercaptan in the presence of a catalytic amount of a quaternary ammonium or phosphonium salt, a tertiary amine or hydrohalide thereof or an alkali metal halide combined with a Crown ether, in the substantial absence of a base.
Process For The Manufacture Of N-(Beta-Diorganodithiophosphorylethyl) Aryl And Alkyl Sulfonamides
Llewellyn W. Fancher - Orinda CA Jeffrey D. Robbins - Berkeley CA
Assignee:
Stauffer Chemical Company - Westport CT
International Classification:
C07F 9165 C07F 932 C07F 940
US Classification:
260938
Abstract:
N-(beta-diorganodithiophosphorylethyl) aryl and alkyl sulfonamides are prepared by a process comprising reacting a compound having the formula R. sup. 1 SO. sub. 2 X with 2-aminoethyl hydrogen sulfate and an aqueous solution of M. sup. 1 OH, and reacting the resulting product with a compound having the formula ##STR1## In the above description, R. sup. 1 is selected from the group consisting of C. sub. 1 -C. sub. 10 alkyl, halo-substituted C. sub. 1 -C. sub. 10 alkyl, phenyl, halo-substituted phenyl, nitro-substituted phenyl, and naphthyl; R. sup. 2 and R. sup. 3 are independently selected from the group consisting of C. sub. 1 -C. sub. 10 alkyl and C. sub. 1 -C. sub. 10 alkoxy; X is selected from the group consisting of chloride, bromide, and iodide; and M. sup. 1 and M. sup. 2 are independently selected from the group consisting of lithium, sodium, potassium, ammonium, and tri-substituted ammonium wherein the substituents are independently C. sub. 1 -C. sub. 10 alkyl.
Method For Preparation Of N-Phosphonomethylglycine
Disclosed is a method for the preparation of N-phosphonomethylglycine which comprises the steps of (1) reacting 1,3,5-tris(alkoxy- or aryloxy-substituted carbonylmethyl) hexahydro-s-triazine, with a substituted phosphorus compound having the formula PXYZ wherein X is a halogen, Y and Z are independently selected from the group consisting of halogen, alkoxy having from 1 to 10 carbon atoms, and aryloxy, in the presence of a protic acid and a low molecular weight carboxylic acid; (2) heating said reactants to a temperature ranging from about 10. degree. to about 25. degree. C. for a sufficient period of time to cause the formation of an N-phosphonomethylglycine ester,; and (3) hydrolyzing said phosphonomethylglycine ester to N-phosphonomethylglycine.
Method For Preparation Of N-Phosphonomethylglycine
A method for the production of N-phosphonomethylglycine which comprises reacting N,N-bis(phosphonomethyl)glycine having the formula ##STR1## with glycine in the presence of a hydrogen ion donor and of water, and at a sufficient temperature and at a sufficient pressure to cause the reaction to go to completion.
Method For Preparation Of N-Phosphonomethylglycine
Disclosed is a method for the preparation of N-phosphonomethylglycine which comprises the steps of (a) reacting 1,3,5-tri-(substituted methyl) hexahydro-s-triazine, a compound of the formula ##STR1## wherein R, R. sub. 1 and R. sub. 2 are the same or different and are selected from the group consisting of cyano, alkoxycarbonyl wherein the alkyl group ranges from 2 to 18 carbon atoms, and aryloxycarbonyl wherein the aryl group ranges from 6 to 12 carbon atoms, with a substituted phosphorus compound having the formula PXYZ wherein X is a halogen, Y and Z are each independently selected from the group consisting of halogen, alkoxy having from 1 to 10 carbon atoms and aryloxy, in the presence of a low molecular weight carboxylic acid solvent and a protic acid; (b) treating the reaction mixture with water; (c) removing said solvent and hydrolyzing the residue with aqueous alkali to generate a salt of N-phosphonomethylglycine; and (d) neutralizing said salt with an acid to produce the end product, N-phosphonomethylglycine.
A novel process for preparing asymmetrical thioureas having the formula ##STR1## is disclosed, which comprises reacting RNH. sub. 2 with CS. sub. 2 in the presence of a base to produce RNHCS. sub. 2. crclbar. followed by reaction of the RNHCS. sub. 2. crclbar. with R. sub. 1 R. sub. 2 NH in the presence of a catalytic amount of a base to produce the desired product.
Process For The Preparation Of 1,1'-Methane-Bis (Hydantoin)
This invention relates to method for the preparation of 1,1'-methane-bis(hydantoin). 1,1'-methane-bis(hydantoin) is an intermediate in the preparation of N-(phosphonomethyl)glycine which is a well known herbicide and plant growth regulator.
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Jeffrey Robbins
Education:
DeSales University - Masters Business Administration, The Art Institute of Pittsburgh - Multimedia & Web Design, South Dakota School of Mines and Technology - Mechanical Engineering