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299162-82-6

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299162-82-6 Usage

General Description

1-(4-chlorophenyl)-5-phenyl-1H-pyrazole, also known as CPP, is an organic compound with the molecular formula C15H11ClN2. This chemical is a pyrazole derivative and belongs to the class of phenylpyrazoles. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. CPP has been studied for its potential pharmacological and biological activities, as it exhibits antinociceptive and anti-inflammatory properties. Additionally, it has been investigated for its potential use as a cannabinoid receptor antagonist. Overall, 1-(4-chlorophenyl)-5-phenyl-1H-pyrazole is a versatile compound with various potential applications in the medical and agricultural fields.

Check Digit Verification of cas no

The CAS Registry Mumber 299162-82-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,9,1,6 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 299162-82:
(8*2)+(7*9)+(6*9)+(5*1)+(4*6)+(3*2)+(2*8)+(1*2)=186
186 % 10 = 6
So 299162-82-6 is a valid CAS Registry Number.

299162-82-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-chlorophenyl)-5-phenylpyrazole

1.2 Other means of identification

Product number -
Other names -

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:299162-82-6 SDS

299162-82-6Downstream Products

299162-82-6Relevant articles and documents

Copper-mediated tandem ring-opening/cyclization reactions of cyclopropanols with aryldiazonium salts: Synthesis of: N -arylpyrazoles

Liu, Jidan,Xu, Erjie,Jiang, Jinyuan,Huang, Zeng,Zheng, Liyao,Liu, Zhao-Qing

, p. 2202 - 2205 (2020/02/26)

A general method for the synthesis of structurally diverse N-arylpyrazoles from readily available cyclopropanols and aryldiazonium salts is disclosed. The reaction was conducted at room temperature within minutes with a broad substrate scope and excellent regioselectivity.

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