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1H-Pyrazolo[3,4-b]pyridine, 3-(phenoxymethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1095223-29-2

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1095223-29-2 Usage

Structure

Pyrazolo[3,4-b]pyridine derivative with a phenoxymethyl group attached to the third position of the pyrazolo ring

Potential applications

Medicinal chemistry, specifically in the development of new drugs

Biological activities and interactions

Of interest for further research and development

Check Digit Verification of cas no

The CAS Registry Mumber 1095223-29-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,5,2,2 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1095223-29:
(9*1)+(8*0)+(7*9)+(6*5)+(5*2)+(4*2)+(3*3)+(2*2)+(1*9)=142
142 % 10 = 2
So 1095223-29-2 is a valid CAS Registry Number.

1095223-29-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(phenoxymethyl)-1H-pyrazolo[3,4-b]pyridine

1.2 Other means of identification

Product number -
Other names -

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:1095223-29-2 SDS

1095223-29-2Downstream Products

1095223-29-2Relevant academic research and scientific papers

Expedient synthesis of 3-alkoxymethyl- And 3-aminomethyl-pyrazolo[3,4-b] pyridines

Beutner, Gregory L.,Kuethe, Jeffrey T.,Kim, Mary M.,Yasuda, Nobuyoshi

supporting information; experimental part, p. 789 - 794 (2009/06/20)

An effective strategy has been developed for the preparation of 3-alkoxymethyl-pyrazolo[3,4-b]pyridines, compounds that are currently not readily accessible by existing synthetic methods. Further manipulation of these compounds allows for access to 3-alkoxymethyl-pyrazolo[3,4-b]pyridines with a variety of substitution patterns as well as 3-aminomethyl-pyrazolo[3,4-b] pyridines.

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