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1217-64-7

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1217-64-7 Usage

Structure

Pyrazole derivative with a pyridine ring and a phenyl group

Use in pharmaceutical research

Being studied for potential medicinal properties

Applications

May be used in drug development and as a building block in the synthesis of other chemical compounds

Biological activities

May exhibit properties of interest to the scientific community

Check Digit Verification of cas no

The CAS Registry Mumber 1217-64-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1217-64:
(6*1)+(5*2)+(4*1)+(3*7)+(2*6)+(1*4)=57
57 % 10 = 7
So 1217-64-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H13N3O/c1-9-8-12(18)13-10(2)16-17(14(13)15-9)11-6-4-3-5-7-11/h3-8,16H,1-2H3

1217-64-7SDS

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 3,6-dimethyl-1-phenyl-2H-pyrazolo[3,4-b]pyridin-4-one

1.2 Other means of identification

Product number -
Other names HMS2293J23

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:1217-64-7 SDS

1217-64-7Downstream Products

1217-64-7Relevant articles and documents

Synthesis and biological activity of new potential antimalarial: 1H- pyrazolo[3,4-b]pyridine derivatives

Dias,Freitas,Barreiro,Goins,Nanayakkara,McChesney

, p. 14 - 20 (2007/10/03)

The appearance of drug resistant Plasmodium falciparum malaria necessitates the search for novel antimalarial agents. Using the classical ring-bioisosterism concept as a strategy to develop new potential drugs, 1H- pyrazolo[3,4-b]pyridine 4-aminomethanol

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