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3-(4-chlorophenyl)[1,2,4]triazolo[4,3-a]pyrimidine, also known as CP-TP, is a heterocyclic organic compound with a molecular formula C10H6ClN5. It belongs to the triazolopyrimidine class and has been studied for its potential pharmaceutical properties, including its role as an anticancer agent.
Used in Pharmaceutical Industry:
3-(4-chlorophenyl)[1,2,4]triazolo[4,3-a]pyrimidine is used as an anticancer agent for its potential to inhibit the growth of cancer cells, particularly in breast and prostate cancer.
Used in Antifungal Applications:
3-(4-chlorophenyl)[1,2,4]triazolo[4,3-a]pyrimidine is used as an antifungal agent for its potential to combat fungal infections.
Used in Antibacterial Applications:
3-(4-chlorophenyl)[1,2,4]triazolo[4,3-a]pyrimidine is used as an antibacterial agent for its potential to fight against bacterial infections.

65267-37-0

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65267-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65267-37-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,6 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65267-37:
(7*6)+(6*5)+(5*2)+(4*6)+(3*7)+(2*3)+(1*7)=140
140 % 10 = 0
So 65267-37-0 is a valid CAS Registry Number.

65267-37-0SDS

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 3-(4-chlorophenyl)-[1,2,4]triazolo[4,3-a]pyrimidine

1.2 Other means of identification

Product number -
Other names 3-p-Chlorphenyl-s-triazolo<4,3-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:65267-37-0 SDS

65267-37-0Relevant academic research and scientific papers

Product and Mechanism of Gas-phase Pyrolysis of 2-arylidinehydrazinopyrimidines: Interesting Route to Condensed Heterocycles [1]

Al-Awadi, Sundus A.,Ibrahim, Maher R.,El-Dusouqui, Osman M. E.,Al-Awadi, Nouria A.

, p. 1812 - 1816 (2015/11/09)

Gas-phase pyrolysis of N-arylidine-N′-pyrimidin-2-yl-hydrazine derivatives 1a, 1b, 1c, 1d, 1e gave the corresponding arylnitriles 2a, 2b, 2c, 2d, 2e, 2-aminopyrimidine 3, 3-phenyl-1,2,4-triazolo[4,3-a]pyrimidines 4, 2-phenyl-1,2,4-triazolo[1,5-a]pyrimidines 5, 2,4,5-triphenyl-1H-imidazole 6, and 2,3-diphenylquinoline 7. The analyses of the reaction products are reported and used to elucidate the mechanism of the pyrolytic process.

A convenient new synthesis of fused 1,2,4-triazoles: The oxidation of heterocyclic hydrazones using copper dichloride

Ciesielski, Michael,Pufky, Daniela,D?ring, Manfred

, p. 5942 - 5947 (2007/10/03)

A series of 1,2,4-triazoles have been prepared by oxidative intramolecular cyclization of heterocyclic hydrazones with copper dichloride. General applicability of this simple transformation was confirmed by the synthesis of moderate to high yields of 1,2,

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