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L-Glutamic acid, N-[(4-nitrophenyl)sulfonyl]-, bis(1,1-dimethylethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

204582-39-8

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204582-39-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 204582-39-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,5,8 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 204582-39:
(8*2)+(7*0)+(6*4)+(5*5)+(4*8)+(3*2)+(2*3)+(1*9)=118
118 % 10 = 8
So 204582-39-8 is a valid CAS Registry Number.

204582-39-8SDS

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 ditert-butyl (2S)-2-[(4-nitrophenyl)sulfonylamino]pentanedioate

1.2 Other means of identification

Product number -
Other names L-Glutamic acid,N-[(4-nitrophenyl)sulfonyl]-,bis(1,1-dimethylethyl) 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:204582-39-8 SDS

204582-39-8Relevant academic research and scientific papers

Synthesis and structure-activity relationships of TAN-1511 analogues as potent hematopoietic agents

Itoh, Fumio,Nishikimi, Yuji,Hasuoka, Atsushi,Yoshioka, Yoshio,Yukishige, Koichi,Tanida, Seiichi,Aono, Tetsuya

, p. 255 - 273 (2007/10/03)

A series of TAN-1511 analogues bearing a non-peptide spacer in place of the Gly-Gly-Gly sequence in the peptide moiety was synthesized, and the effects of these compounds on the proliferation of bone marrow cells in culture and experimental leukocytopenia in mice were examined. The structure- activity relationships obtained were as follows. As the substituent at the 2- position of the 4-thiabeptanoic acid framework, an amino group, methyl group or hydrogen was preferable; as a spacer in place of the Gly-Gly-Gly sequence, a 4-aminobenzoyl or 4-aminomethylbenzoyl group was suitable; and as the fatty acids bonded to the 6,7-dihydroxy groups, C16 fatty acid was best. Compounds 12f, 30d and 30i potently promoted the proliferation of bone marrow cells in culture and the restoration of leukocyte counts in a murine leukocytopenia model.

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