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100960-07-4

100960-07-4

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100960-07-4 Usage

Chemical Properties

Brown crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 100960-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,9,6 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 100960-07:
(8*1)+(7*0)+(6*0)+(5*9)+(4*6)+(3*0)+(2*0)+(1*7)=84
84 % 10 = 4
So 100960-07-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3/c8-6-3-5-1-2-9-7(5)10-4-6/h1-4H,8H2,(H,9,10)

100960-07-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail

  • Alfa Aesar

  • (H35382)  5-Amino-7-azaindole, 97%   

  • 100960-07-4

  • 250mg

  • 1999.0CNY

  • Detail

  • Alfa Aesar

  • (H35382)  5-Amino-7-azaindole, 97%   

  • 100960-07-4

  • 1g

  • 5569.0CNY

  • Detail

  • Aldrich

  • (ADE000889)  1H-Pyrrolo[2,3-b]pyridin-5-ylamine  AldrichCPR

  • 100960-07-4

  • ADE000889-1G

  • 7,411.95CNY

  • Detail

100960-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Amino-7-azaindole

1.2 Other means of identification

Product number -
Other names 1H-PYRROLO[2,3-B]PYRIDIN-5-YLAMINE

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:100960-07-4 SDS

100960-07-4Relevant articles and documents

A practical, efficient synthesis of 5-amino-7-azaindole

Pearson, Stuart E.,Nandan, Santosh

, p. 2503 - 2506 (2005)

A much improved, workable synthesis of 5-amino-7-azaindole is described in 66% overall yield starting from 2-amino-5-nitropyridine. The key stage involves a microwave promoted heteroannulation reaction of a pyridine alkyne. Georg Thieme Verlag Stuttgart.

AZABENZIMIDAZOLES AND THEIR USE AS AMPA RECEPTOR MODULATORS

-

Page/Page column 98; 99, (2016/11/17)

Provided herein are compounds of Formula (I), and pharmaceutically acceptable salts, N-oxides, or solvates thereof, [formula (I) should be inserted here]. Also provided herein are pharmaceutical compositions comprising compounds of Formula (I) and methods

7-azaindol-3-ylacrylamides active as kinase inhibitors

-

Page/Page column 92, (2009/07/10)

Compounds represented by Formula (I) wherein R1 and R2 are as defined in the specification, compositions thereof, and methods of use thereof.

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