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29912-57-0

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29912-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29912-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,9,1 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29912-57:
(7*2)+(6*9)+(5*9)+(4*1)+(3*2)+(2*5)+(1*7)=140
140 % 10 = 0
So 29912-57-0 is a valid CAS Registry Number.

29912-57-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-5-(4-aminobutyl)-3-phenyl-2-thioxoimidazolidin-4-one

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:29912-57-0 SDS

29912-57-0Downstream Products

29912-57-0Relevant articles and documents

Simple and Efficient Synthesis of 5-Substituted-3-phenyl-2-thioxoimidazolidin-4-one Derivatives from S -Amino Acids and Phenylisothiocyanate in et 3N/DMF-H 2O

Jangale, Asha D.,Wagh, Yogesh B.,Tayade, Yogesh A.,Dalal, Dipak S.

supporting information, p. 1876 - 1886 (2015/08/03)

A concise approach for the transformation of various S-amino acids into the 5-alkyl-3-phenyl-2-thioxoimidazolidin-4-one heterocycles using phenylisothiocyanate is described. Phenylthiohydantoins of amino acid were synthesized at room temperature in Et3N/DMF-H2O with easy workup and excellent yields.

Incorporation of phosphorylation sites

-

Page column 12, (2008/06/13)

A reagent is described for incorporating phosphorylation sites into compounds, particularly into proteins and peptides. The reagent has the structure A—B—C wherein A is a moiety that is specifically reactive with a reactive side chain in the compound, B is a linking moiety, and C is a peptide sequence that contains a kinase substrate.

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