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400900-22-3

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400900-22-3 Usage

Chemical structure

A pyrazole derivative with a benzoyl and phenyl substituent

Usage

Often used in organic synthesis and pharmaceutical research as a building block for the preparation of various biologically active compounds

Potential applications

Development of new drugs and agrochemicals, materials science, and related fields

Unique features

Versatile chemical with diverse potential applications in various scientific and industrial fields

Check Digit Verification of cas no

The CAS Registry Mumber 400900-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,9,0 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 400900-22:
(8*4)+(7*0)+(6*0)+(5*9)+(4*0)+(3*0)+(2*2)+(1*2)=83
83 % 10 = 3
So 400900-22-3 is a valid CAS Registry Number.

400900-22-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzoyl-1-phenylpyrazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1H-Pyrazole-4-carboxaldehyde,3-benzoyl-1-phenyl

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:400900-22-3 SDS

400900-22-3Downstream Products

400900-22-3Relevant articles and documents

Polyfunctional pyrazoles. 2. 1-Aryl-3-benzoyl-4-formyl- and 4-carboxypyrazoles

Bratenko,Chornous,Vovk

, p. 467 - 469 (2001)

Cyclization of 1-phenylpropane-1,2-dione monoarylhydrazones under Vilsmeier-Haack conditions gave 1-aryl-3-benzoyl-4-formylpyrazoles which were converted to 1-aryl-3-benzoyl-4-carboxyprazoles using potassium permanganate in aqueous pyridine medium.

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