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556104-19-9

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556104-19-9 Usage

Molecular weight

146.19 g/mol

Structure

A heterocyclic amine with a pyrrolopyridine core structure

Biological activity

Potential as an antiviral and anticancer agent

Medicinal chemistry and drug development

Has been studied as a building block for the synthesis of pharmaceutical compounds

Organic synthesis

Has been explored for use in organic synthesis

Coordination chemistry

Has been investigated as a ligand in coordination chemistry

Applications

Diverse applications in various fields of chemistry and biology.

Check Digit Verification of cas no

The CAS Registry Mumber 556104-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,6,1,0 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 556104-19:
(8*5)+(7*5)+(6*6)+(5*1)+(4*0)+(3*4)+(2*1)+(1*9)=139
139 % 10 = 9
So 556104-19-9 is a valid CAS Registry Number.

556104-19-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-aminomethyl-7-azaindoline

1.2 Other means of identification

Product number -
Other names 1H-Pyrrolo[2,3-b]pyridine-5-methanamine,2,3-dihydro-

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:556104-19-9 SDS

556104-19-9Relevant articles and documents

Azaindoles: Moderately basic P1 groups for enhancing the selectivity of thrombin inhibitors

Sanderson, Philip E. J.,Stanton, Matthew G.,Dorsey, Bruce D.,Lyle, Terry A.,McDonough, Colleen,Sanders, William M.,Savage, Kelly L.,Naylor-Olsen, Adel M.,Krueger, Julie A.,Lewis, S. Dale,Lucas, Bobby J.,Lynch, Joseph J.,Yan, Youwei

, p. 795 - 798 (2007/10/03)

Starting from a 2-amino-6-methylpyridine P1 group and following a strategy of enlarging it whilst reducing its polarity, we have developed a series of potent, moderately basic azaindoles which are intrinsically much more selective for thrombin versus tryp

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