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6-Chloro-N-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine is a chemical compound with the molecular formula C6H6ClN5. It is a derivative of pyrazolo[3,4-d]pyrimidin-4-amine, featuring a 6-chloro substituent and an N-methyl group. This heterocyclic compound is characterized by its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various biologically active molecules. Its structure consists of a pyrazolo[3,4-d]pyrimidine core, which is fused to a pyrazole ring, and the presence of the chlorine atom and methyl group provides opportunities for further functionalization and modification. The compound's properties, such as solubility and reactivity, can be influenced by these substituents, making it a versatile intermediate in the development of new pharmaceuticals and agrochemicals.

7251-92-5

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7251-92-5 Usage

Chemical Structure

It contains a pyrazolo[3,4-d]pyrimidine core structure with a chlorine atom at the 6th position and a methyl group at the N position.

Functional Groups

Contains an amine group due to the presence of an amino group.

Application

Widely utilized in the pharmaceutical industry for developing potential drug candidates, especially for targeting specific biological pathways.

Safety Precautions

Due to its chemical properties, it requires careful handling and adherence to safety protocols in laboratory settings.

Check Digit Verification of cas no

The CAS Registry Mumber 7251-92-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7251-92:
(6*7)+(5*2)+(4*5)+(3*1)+(2*9)+(1*2)=95
95 % 10 = 5
So 7251-92-5 is a valid CAS Registry Number.

7251-92-5SDS

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 6-chloro-N-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine

1.2 Other means of identification

Product number -
Other names (6-Chlor-1(2)H-pyrazolo[3,4-d]pyrimidin-4-yl)-methyl-amin

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:7251-92-5 SDS

7251-92-5Downstream Products

7251-92-5Relevant academic research and scientific papers

LRRK2 INHIBITORS AND METHODS OF MAKING AND USING THE SAME

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, (2016/09/22)

Compounds having the formula (I), (II), (III) are provided. Compounds of the present disclosure are useful for the treatment of neurodegenerative diseases, such as Parkinson's Disease.

Discovery of a pyrrolopyrimidine (JH-II-127), a highly potent, selective, and brain penetrant LRRK2 inhibitor

Hatcher, John M.,Zhang, Jinwei,Choi, Hwan Geun,Ito, Genta,Alessi, Dario R.,Gray, Nathanael S.

, p. 584 - 589 (2015/05/27)

Activating mutations in leucine-rich repeat kinase 2 (LRRK2) are present in a subset of Parkinson's disease (PD) patients and may represent an attractive therapeutic target. Here we report a 2-anilino-4-methylamino-5-chloropyrrolopyrimidine, JH-II-127 (18

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