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92234-23-6

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92234-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92234-23-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,3 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 92234-23:
(7*9)+(6*2)+(5*2)+(4*3)+(3*4)+(2*2)+(1*3)=116
116 % 10 = 6
So 92234-23-6 is a valid CAS Registry Number.

92234-23-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-bromo-2-hydroxy propionate

1.2 Other means of identification

Product number -
Other names 3-Bromo-2-hydroxy-propionic acid ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:92234-23-6 SDS

92234-23-6Relevant articles and documents

Synthesis of 4,6-unsubstituted 2-aminodihydropyrimidine-5-carboxylates through sequential staudinger/aza-wittig/cyclization reactions

Nishimura, Yoshio,Cho, Hidetsura

, p. 233 - 237 (2015)

A novel method for constructing the dihydropyrimidine skeleton is developed. The method involves three sequential reactions: (1) the Staudinger reaction of (E)-ethyl 3-azido-2-{[(tert-butoxycarbonyl)amino]methyl}acrylate with triphenylphosphine; (2) aza-W

HIV INTEGRASE INHIBITORS

-

Page/Page column 54; 55, (2008/06/13)

Bicyclic pyrazoles of Formula I are inhibitors of HIV integrase and inhibitors of HIV replication: (I), wherein Z is O or N(R8); n is an integer equal to zero or 1; and R1, R2, R3, R4, R5, R6, R7 and R8 are defined herein. The compounds are useful in the prevention and treatment of infection by HIV and in the prevention, delay in the onset, and treatment of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines.

Synthese et polymerisation de monomeres fluores acryliques substitues en position α. Partie III. Synthese et polymerisation de l'α-heptadecafluoro-undecanoyloxyacrylate d'ethyle

Bessiere, J. M.,Boutevin, B.,El Bachiri, A.,El Harfi, A.

, p. 91 - 96 (2007/10/02)

The synthesis of ethyl α-heptadecafluoro-undecanoyloxyacrylate (3), H2C=C(O-CO-CH2CH2C8F17)CO2CH2CH3, has been performed in three steps starting from ethyl bromopyruvate and heptadecafluoro-undecanoic acid, with an overall yield of c. 70percent.The homopolymerization and copolymerization of 3 have been easily carried out.From the kinetic study of homopolymerization and copolymerization of monomer 3 with styrene, kp2/kTe and r1, r2, the reactivity ratios of the two monomers, can be determined.

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