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4-Pentenoic acid, 2-amino-5-phenyl-, 1,1-dimethylethyl ester, (2R,4E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

923276-11-3

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923276-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 923276-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,2,7 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 923276-11:
(8*9)+(7*2)+(6*3)+(5*2)+(4*7)+(3*6)+(2*1)+(1*1)=163
163 % 10 = 3
So 923276-11-3 is a valid CAS Registry Number.

923276-11-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-1-cinnamyl glycine tert-butyl ester

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:923276-11-3 SDS

923276-11-3Downstream Products

923276-11-3Relevant academic research and scientific papers

PROCESS FOR PRODUCTION OF MONO-SUBSTITUTED ALKYLATED COMPOUND USING ALDIMINE OR DERIVATIVE THEREOF

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Page/Page column 103-104, (2008/06/13)

Disclosed is a process for producing an asymmetric mono-substituted alkylated compound of an α-amino acid which is represented by a specific formula by using an aldimine-type Schiff base. In the process, the alkylation of an aldimine-type Schiff base in a medium in the presence of an optically active quaternary ammonium salt phase transfer catalyst and an inorganic base is started, and subsequently the reaction is quenched at any time preceding the completion of the stoichimetrical reaction, thereby yielding a mono-substituted alkylated product having a high optical purity.

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