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102839-56-5

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102839-56-5 Usage

General Description

1H-Pyrrolo[3,2-c]pyridin-4-amine,1-methyl-(9CI) is a chemical compound with the molecular formula C11H10N4. It is a heterocyclic amine with a pyrrolopyridine core structure. 1H-Pyrrolo[3,2-c]pyridin-4-amine,1-methyl-(9CI) is also known as CPT, and it is a potent inhibitor of the DNA repair enzyme poly(ADP-ribose) polymerase (PARP). CPT has been studied for its potential applications in cancer therapy, as it can selectively kill cancer cells that have defects in DNA repair mechanisms. It has also shown promise in combination therapy with other chemotherapy agents. Overall, 1H-Pyrrolo[3,2-c]pyridin-4-amine,1-methyl-(9CI) has attracted attention for its potential role in cancer treatment and further research in this area is ongoing.

Check Digit Verification of cas no

The CAS Registry Mumber 102839-56-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,8,3 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 102839-56:
(8*1)+(7*0)+(6*2)+(5*8)+(4*3)+(3*9)+(2*5)+(1*6)=115
115 % 10 = 5
So 102839-56-5 is a valid CAS Registry Number.

102839-56-5SDS

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 1-Methyl-1H-pyrrolo[3,2-c]pyridin-4-amine

1.2 Other means of identification

Product number -
Other names 1H-Pyrazolo[3,4-d]pyridazin-4-amine,1-methyl

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:102839-56-5 SDS

102839-56-5Downstream Products

102839-56-5Relevant articles and documents

The Synthesis of 5-Azaindoles by Substitution-Rearrangement of 7-Azaindoles upon Treatment with Certain Primary Amines

Girgis, Nabih S.,Larson, Steven B.,Robins, Roland K.,Cottam, Howard B.

, p. 317 - 325 (2007/10/02)

Certain 4-substituted 1H-pyrrolopyridines (7-azaindoles) undergo a nucleophilic substitution-rearrangement upon treatment with various primary amines at elevated temperatures to yield N-1-substituted 4-amino-1H-pyrrolopyridines (5-azaindoles).Treatment of the same 7-azaindoles with secondary amines under the same reaction conditions led to simple nucleophilic substitution products.

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