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Methanone, [4-ethoxy-1-(2-furanylmethyl)-1H-pyrazolo[3,4-b]pyridin-5-yl]phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56352-01-3

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56352-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56352-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,5 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56352-01:
(7*5)+(6*6)+(5*3)+(4*5)+(3*2)+(2*0)+(1*1)=113
113 % 10 = 3
So 56352-01-3 is a valid CAS Registry Number.

56352-01-3SDS

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 5-benzoyl-4-ethoxy-1-(2-furanyl)methyl-1H-pyrazolo[3,4-b]-pyridine

1.2 Other means of identification

Product number -
Other names 5-Benzoyl-4-ethoxy-1-(furan-2-yl)methyl-1H-pyrazolo[3,4-b]pyridine

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:56352-01-3 SDS

56352-01-3Relevant academic research and scientific papers

Alcohol derivatives of pyrazolo[3,4-b]pyridines

-

, (2008/06/13)

Alcohol derivatives of pyrazolo[3,4-b]pyridines having the formula SPC1 And their acid addition salts are disclosed. The novel compounds are useful as central nervous system depressants and anti-inflammatory agents. In addition, the new compounds increase

Method for producing 1-unsubstituted pyrazolo[3,4-b]pyridine ketones

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, (2008/06/13)

A new process for the production of pyrazolo-[3,4-b]pyridine ketones which are unsubstituted in the 1-position comprises reacting a 1-furanylmethylpyrazolo[3,4-b]pyridine ketone with an inorganic strong mineral acid like sulfuric acid, phosphoric acid or polyphosphoric acid.

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