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245325-32-0

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245325-32-0 Usage

Chemical Class

Pyrazole derivatives

Type of Compound

Nitrogen-containing heterocyclic compound

Structure

Pyrazole ring fused to a pyridine ring

Chlorine atom position

5th position of the pyrazole ring

Potential Applications

Medicinal chemistry, pharmaceutical drug development

Unique structure and properties

Interesting target for research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 245325-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,3,2 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 245325-32:
(8*2)+(7*4)+(6*5)+(5*3)+(4*2)+(3*5)+(2*3)+(1*2)=120
120 % 10 = 0
So 245325-32-0 is a valid CAS Registry Number.

245325-32-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-5-chloro-1H-pyrazolo[3,4-c]pyridine

1.2 Other means of identification

Product number -
Other names 5-chloro-1H-pyrazolo[3,4-c]pyridin-3-amine

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:245325-32-0 SDS

245325-32-0Downstream Products

245325-32-0Relevant articles and documents

Synthesis, reactivity and 13C-NMR of 1H-pyrazolo[3,4-c]pyridine derivatives

Milhavet, Jean-Claude,Gueiffier, Alain,Bernal, Lysiane,Teulade, Jean-Claude

, p. 1661 - 1667 (2007/10/03)

The synthesis of various 1H-pyrazolo [.-c.]pyridines was reported. 3- Cyano derivatives were obtained from the corresponding nitro compounds by Sandmeyer Reaction using Na3[Cu(CN)4] at pH 1. The 13C-NMR data of this series were also described.

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