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2,5-DIMETHYLPYRAZOLO[1,5-A]PYRIMIDIN-7-AMINE is a chemical compound with the molecular formula C8H10N6. It is a pyrazolopyrimidine derivative, which means it is a heterocyclic organic compound containing a pyrazole and pyrimidine ring system. 2,5-DIMETHYLPYRAZOLO[1,5-A]PYRIMIDIN-7-AMINE has potential applications in the pharmaceutical industry due to its structural features and potential biological activities. It may be used in the development of new drugs or as a research tool in the study of biological pathways and interactions. However, the specific properties and uses of 2,5-DIMETHYLPYRAZOLO[1,5-A]PYRIMIDIN-7-AMINE have not been extensively studied, and further research is needed to fully understand its potential applications.

2369-89-3

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2369-89-3 Usage

Uses

Used in Pharmaceutical Industry:
2,5-DIMETHYLPYRAZOLO[1,5-A]PYRIMIDIN-7-AMINE is used as a potential drug candidate for the development of new medications. Its unique structure and potential biological activities make it a promising compound for further research and development in the pharmaceutical field.
Used in Research and Development:
2,5-DIMETHYLPYRAZOLO[1,5-A]PYRIMIDIN-7-AMINE is used as a research tool for studying biological pathways and interactions. Its heterocyclic structure and potential activities may provide insights into various biological processes, contributing to the advancement of scientific knowledge in the field of chemistry and biology.

Check Digit Verification of cas no

The CAS Registry Mumber 2369-89-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,6 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2369-89:
(6*2)+(5*3)+(4*6)+(3*9)+(2*8)+(1*9)=103
103 % 10 = 3
So 2369-89-3 is a valid CAS Registry Number.

2369-89-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-Dimethylpyrazolo[1,5-a]pyrimidin-7-amine

1.2 Other means of identification

Product number -
Other names 2.5-Dimethyl-7-amino-pyrazolo-<1.5-a>pyrimidin

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:2369-89-3 SDS

2369-89-3Downstream Products

2369-89-3Relevant academic research and scientific papers

7-Amino-2,5-dimethylpyrazolo[1,5-a]-pyrimidine hemihydrate redetermined at 120 K: A three-dimensional hydrogen-bonded framework

Portilla, Jaime,Quiroga, Jairo,Cobo, Justo,Low, John N.,Glidewell, Christopher

, p. o186-o189 (2006)

In the title compound, C8H10N4·0. 5H2O, where the water molecules lie on twofold rotation axes in the space group C2, the components are linked by three hydrogen bonds, one each of O-H...N, N-H...N and N-H...O types, into a complex three-dimensional framework structure.

Synthesis of novel 5-amino-1-aroylpyrazoles

Quiroga, Jairo,Portilla, Jaime,Abonía, Rodrigo,Insuasty, Braulio,Nogueras, Manuel,Cobo, Justo

body text, p. 5943 - 5945 (2009/04/11)

A series of 5-amino-1-aroylpyrazoles 3 are synthesized directly by the reaction of β-aminocrotononitrile 1 with some structures containing the hydrazine moiety (X-NHNH2) 2 by refluxing ethanol in presence of sodium acetate. When semicarbazide 3i was used (X = CONH2), the reaction afforded the unexpected 7-aminopyrazolo[1,5-a]pyrimidine 4.

Pyrazolo[1,5-a]pyrido[3,2-e]pyrimidine-7-carboxylic acid derivatives

-

, (2008/06/13)

New derivatives of pyrazolo[1,5-a]pyrido[3,2-e]-pyrimidine-7-carboxylic acid have the general formula STR1 The new compounds are useful as central nervous system depressants and an anti-inflammatory agents.

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