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7-chloro-1-methyl-1H-pyrazolo[4,3-d]pyrimidine is a heterocyclic compound characterized by a pyrazolo[4,3-d]pyrimidine backbone, featuring a chlorine and a methyl substituent. As a nitrogen-containing organic compound, it demonstrates potential for interaction with biological systems, making it a promising candidate for various applications, particularly in the pharmaceutical industry. The chlorine atom enhances the molecule's reactivity, allowing for a range of chemical reactions, while the methyl group adds to the structural diversity and the potential for interactions with other compounds. This unique chemical structure positions 7-chloro-1-methyl-1H-pyrazolo[4,3-d]pyrimidine as an interesting target for research and development in the creation of novel pharmaceuticals, agrochemicals, or materials with specific properties.

923282-39-7

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923282-39-7 Usage

Uses

Used in Pharmaceutical Industry:
7-chloro-1-methyl-1H-pyrazolo[4,3-d]pyrimidine is used as a chemical intermediate for the synthesis of various pharmaceutical compounds due to its ability to interact with biological systems. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Development:
In the agrochemical industry, 7-chloro-1-methyl-1H-pyrazolo[4,3-d]pyrimidine is used as a building block for the creation of novel agrochemicals. Its reactivity and structural diversity contribute to the design of new pesticides or herbicides with improved efficacy and selectivity.
Used in Material Science:
7-chloro-1-methyl-1H-pyrazolo[4,3-d]pyrimidine is utilized as a component in the development of new materials with specific properties. Its potential interactions with other compounds make it suitable for use in the creation of advanced materials for various applications, such as sensors, catalysts, or functional coatings.
Used in Chemical Research:
As a heterocyclic compound with a unique structure, 7-chloro-1-methyl-1H-pyrazolo[4,3-d]pyrimidine serves as a subject of interest in chemical research. It is used to explore new chemical reactions, investigate its reactivity, and understand its interactions with biological systems, which can lead to the discovery of new applications and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 923282-39-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,2,8 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 923282-39:
(8*9)+(7*2)+(6*3)+(5*2)+(4*8)+(3*2)+(2*3)+(1*9)=167
167 % 10 = 7
So 923282-39-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H5ClN4/c1-11-5-4(2-10-11)8-3-9-6(5)7/h2-3H,1H3

923282-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Chloro-1-methyl-1H-pyrazolo[4,3-d]pyrimidine

1.2 Other means of identification

Product number -
Other names 7-chloro-1-methylpyrazolo[4,3-d]pyrimidine

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:923282-39-7 SDS

923282-39-7Relevant academic research and scientific papers

ECTONUCLEOTIDE PYROPHOSPHATASE/PHOSPHODIESTERASE 1 (ENPP1) MODULATORS AND USES THEREOF

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Paragraph 00443, (2021/07/02)

Provided herein are small molecule modulators of ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1), compositions comprising the compounds, and methods of using the compounds and compositions comprising the compounds.

Pyrazolo pyrimidines useful as aurora kinase inhibitors

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Page/Page column 80, (2010/11/25)

The present invention provides compounds having the formula: wherein A-B together represent one of the following structures: wherein one of is a double bond, as valency permits; and R2, R4, X1A, X2A, X1B, X2B, L1, L2, Y and Z are as defined in classes and subclasses herein, and pharmaceutical compositions thereof, as described generally and in subclasses herein, which compounds are useful as inhibitors of protein kinase (e.g., Aurora), and thus are useful, for example, for the treatment of Aurora mediated diseases.

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