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119368-04-6

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119368-04-6 Usage

Class

pyrazolo[3,4-b]pyridine derivatives

Structural characteristic

a pyrazole ring fused to a pyridine ring

Substitution

phenylmethoxy group attached to the fourth carbon atom of the pyrazole ring

Potential pharmaceutical applications

ability to interact with biological targets, such as receptors or enzymes, leading to a wide range of biological activities

Influence on pharmacokinetic properties

presence of the phenylmethoxy group can affect solubility, permeability, and metabolic stability

Research and development importance

interesting target in the field of medicinal chemistry due to its structure and potential biological activities

Check Digit Verification of cas no

The CAS Registry Mumber 119368-04-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,3,6 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 119368-04:
(8*1)+(7*1)+(6*9)+(5*3)+(4*6)+(3*8)+(2*0)+(1*4)=136
136 % 10 = 6
So 119368-04-6 is a valid CAS Registry Number.

119368-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(Benzyloxy)-1H-pyrazolo<3,4-b>pyridine

1.2 Other means of identification

Product number -
Other names 4-Benzyloxy-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:119368-04-6 SDS

119368-04-6Relevant articles and documents

Synthesis and biological evaluation of certain C-4 substituted pyrazolo[3,4-b]pyridine nucleosides

Sanghvi,Larson,Willis,Robins,Revankar

, p. 945 - 951 (1989)

A series of C-4 substituted pyrazolo[3,4-b]pyridine nucleosides have been synthesized and evaluated for their biological activity. Successful synthesis of various C-4 substituted pyrazolo[3,4-b]pyridine nucleosides involves nucleophilic displacement by a

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