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2-Pyridinecarboxamide, N-[(1S)-1-[[[(1S,2S)-3-[[(1S)-2-amino-1-[(4-bromophenyl)methyl]-2-oxo ethyl]amino]-2-hydroxy-1-(phenylmethyl)propyl]amino]carbonyl]-2-methyl propyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

500767-38-4

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500767-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 500767-38-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,7,6 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 500767-38:
(8*5)+(7*0)+(6*0)+(5*7)+(4*6)+(3*7)+(2*3)+(1*8)=134
134 % 10 = 4
So 500767-38-4 is a valid CAS Registry Number.

500767-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Pyridine-2-carboxylic acid ((S)-1-{(1S,2S)-1-benzyl-3-[(S)-2-(4-bromo-phenyl)-1-carbamoyl-ethylamino]-2-hydroxy-propylcarbamoyl}-2-methyl-propyl)-amide

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:500767-38-4 SDS

500767-38-4Downstream Products

500767-38-4Relevant academic research and scientific papers

Design and synthesis of plasmepsin I and plasmepsin II inhibitors with activity in Plasmodium falciparum-infected cultured human erythrocytes

N?teberg, Daniel,Hamelink, Elizabeth,Hultén, Johan,Wahlgren, Mats,Vrang, Lotta,Samuelsson, Bertil,Hallberg, Anders

, p. 734 - 746 (2007/10/03)

A series of protease inhibitors targeted at the malarial enzymes plasmepsin I and II, and encompassing a basic hydroxyethylamine transition state isostere scaffold, was prepared. The substituents in the P1′ position were varied and the biological activiti

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