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N-[(Z)-2-(3,4-dimethoxyphenyl)ethenyl]benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128737-83-7

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128737-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128737-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,7,3 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 128737-83:
(8*1)+(7*2)+(6*8)+(5*7)+(4*3)+(3*7)+(2*8)+(1*3)=157
157 % 10 = 7
So 128737-83-7 is a valid CAS Registry Number.

128737-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(Z)-2-(3,4-dimethoxyphenyl)ethenyl]benzamide

1.2 Other means of identification

Product number -
Other names -

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:128737-83-7 SDS

128737-83-7Relevant academic research and scientific papers

Asymmetric hydroformylation of Z -Enamides and enol esters with rhodium-bisdiazaphos catalysts

Abrams, M. Leigh,Foarta, Floriana,Landis, Clark R.

, p. 14583 - 14588 (2014)

Asymmetric hydroformylation (AHF) of Z-enamides and Z-enol esters provides chiral, alpha-functionalized aldehydes with high selectivity and atom economy. Rh-bisdiazaphospholane catalysts enable hydroformylation of these challenging disubstituted substrates under mild reaction conditions and low catalyst loadings. The synthesis of a protected analog of l-DOPA demonstrates the utility of AHF for enantioselective, atom-efficient synthesis of peptide precursors.

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