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L-Phenylalanine, N-[[2-[[(phenylmethoxy)carbonyl]amino]ethyl]sulfonyl]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89343-97-5

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89343-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89343-97-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,4 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89343-97:
(7*8)+(6*9)+(5*3)+(4*4)+(3*3)+(2*9)+(1*7)=175
175 % 10 = 5
So 89343-97-5 is a valid CAS Registry Number.

89343-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyloxycarbonyl-tauryl-L-phenylalanine methyl ester

1.2 Other means of identification

Product number -
Other names (S)-2-(2-Benzyloxycarbonylamino-ethanesulfonylamino)-3-phenyl-propionic acid methyl 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:89343-97-5 SDS

89343-97-5Relevant academic research and scientific papers

Pepstatin Analogues as Novel Renin Inhibitors

Guegan, Remy,Diaz, Joseph,Cazaubon, Catherine,Beaumont, Michel,Carlet, Claude,et al.

, p. 1152 - 1159 (2007/10/02)

Pepstatin analogues corresponding to the general formula A-X-Y-Sta-Ala-Sta-R were synthesized in solution phase.Various changes in the nature of the A, X, and Y groups were made to improve the inhibitory potency against human plasma renin activity.The res

New analogs of somatostatin with unexpected effects in vivo on insulin basal secretion in the rat

Diaz,Cazaubon,Demarne,et al.

, p. 219 - 227 (2007/10/02)

Twenty analogs of somatostatin were synthesized by the alternating solution/solid-phase procedure. The peptide analogs contained taurine, aza-alanine, or D-amino acids as well as multiple deletions. The aim of this study was to obtain analogs that would selectively inhibit insulin or glucagon release. The biological activities were evaluated in vivo in the rat by measuring the effects of the modified somatostatin molecules on basal secretion of insulin and glucagon in the portal vein. Although some selective analogs were found, a few of them having a taurine or an aza-alanine residue in their structure caused a significant increase of insulin secretion. This unexpected phenomenon, for which we do not have an explanation at present, is under investigation.

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