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53685-84-0

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53685-84-0 Usage

Chemical class

Pyrazole derivative

Structural features

Three phenyl groups attached to the central pyrazole ring
Carboxylic acid group at the 4-position

Potential applications

Medicinal chemistry

Biological activities studied

Anti-inflammatory properties
Anti-cancer properties

Possible use

Building block for the synthesis of other biologically active compounds

Relevance

Interesting target for research and development in pharmaceutical and medical fields due to its unique structure and potential pharmacological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 53685-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,8 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53685-84:
(7*5)+(6*3)+(5*6)+(4*8)+(3*5)+(2*8)+(1*4)=150
150 % 10 = 0
So 53685-84-0 is a valid CAS Registry Number.

53685-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-triphenylpyrazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1,3,5-Triphenyl-1H-pyrazol-4-carbonsaeure

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:53685-84-0 SDS

53685-84-0Relevant articles and documents

1,3-Dipolar Cycloaddition of Benzonitrilium N-Phenylimide with 4-Arylmethylidene-3-phenylisoxazol-5(4H)-ones

Abbass, Ikhlass M.,Mosselhi, Mosselhi A. N.,Abdallah, Magda A.,Shawali, Ahmad S.

, p. 190 - 191 (2007/10/03)

The title reaction, when carried out in benzene and in the presence of triethylamine, afforded 5-aryl-1,3-diphenylpyrazole-4-carboxylic acids 11 in 50-60percent yields.

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