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2-Propenoic acid, 3-cyano-3-phenyl-, ethyl ester, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61212-23-5

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61212-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61212-23-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,1 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61212-23:
(7*6)+(6*1)+(5*2)+(4*1)+(3*2)+(2*2)+(1*3)=75
75 % 10 = 5
So 61212-23-5 is a valid CAS Registry Number.

61212-23-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-cyano-3-phenylprop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid,3-cyano-3-phenyl-,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:61212-23-5 SDS

61212-23-5Downstream Products

61212-23-5Relevant academic research and scientific papers

Rhodium(II)-catalyzed cross-coupling of diazo compounds

Hansen, Joorn H.,Parr, Brendan T.,Pelphrey, Philip,Jin, Quihui,Autschbach, Jochen,Davies, Huw M. L.

supporting information; experimental part, p. 2544 - 2548 (2011/04/27)

Nothing left to chance: A convenient protocol for selective cross-coupling of diazo compounds for the convergent synthesis of alkenes was developed (see scheme; EDG=aryl, heteroaryl, vinyl; R=O-alkyl, aryl). The selectivity control elements were identifie

Stereoselective preparation of highly functionalized (Z)-3-magnesiated enoates by an iodine - Magnesium exchange reaction

Sapountzis,Dohle,Knochel

, p. 2068 - 2069 (2007/10/03)

3-Iodoenoates are converted into the corresponding alkenylmagnesium species with complete retention of configuration of the double bond; both direct reaction and copper(I)-mediated reactions with various electrophiles provide polyfunctional enoates.

3α-Arylhydroisoindoles

-

, (2008/06/13)

Certain 3α-arylhydroisoindoles are useful as analgesics and/or narcotic antagonists. Exemplary is N-cyclopropylmethyl-3α-(m-methoxyphenyl)-5,6-dimethyl-2,3,3α,4,7,7α-trans-hexahydroisoindole.

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