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2-Propenoic acid, 2-[(phenylthio)methyl]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82850-01-9

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82850-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82850-01-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,5 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82850-01:
(7*8)+(6*2)+(5*8)+(4*5)+(3*0)+(2*0)+(1*1)=129
129 % 10 = 9
So 82850-01-9 is a valid CAS Registry Number.

82850-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2-(phenylthiomethyl)prop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Phenylsulfanylmethyl-acrylic 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:82850-01-9 SDS

82850-01-9Relevant academic research and scientific papers

An efficient and simple strategy toward the synthesis of highly functionalized compounds

Jmai, Momtez,Efrit, Mohamed Lotfi,Dubreuil, Didier,Blot, Virginie,Lebreton, Jacques,M'rabet, Hédi

, p. 978 - 995 (2021/08/06)

The expedient syntheses of small libraries of ((β-ethoxycarbonyl, -cyano and -acetyl)propyloxy) methylphosphonate scaffolds bearing olefin, sulfanyl, or amine functions are described. All these new derivatives are readily produced from easily available starting reagents (aldehydes, electron-poor olefins, and dialkylphosphites) following a three steps reaction sequence of condensations, SN2′-type reaction and a conjugated thia- or aza-Michael 1,4-addition with aromatic and aliphatic thiol or amine nucleophiles.

Expedient Synthesis of Natural (S)-Sinefungin and of its C-6' Epimer

Barton, Derek H. R.,Gero, Stephane D.,Quiclet-Sire, Beatrice,Samadi, Mohammed

, p. 981 - 985 (2007/10/02)

Sinefungin 1a and 6-epi-sinefungin 1b have been prepared from adenosine and L-aspartic acid.The key step in the synthesis was the coupling of the radical derived from 14 with the unsaturated amide 13.The latter was obtained by a radical reaction from L-as

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