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89193-18-0

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89193-18-0 Usage

Structure

1H-Pyrazole-4-carboxylic acid, 3,5-dimethyl-1-phenyl-, ethyl ester

Classification

Pyrazole derivative

Usage

Building block for the synthesis of biologically active compounds in the pharmaceutical industry

Potential applications

Development of new drugs and pharmaceuticals, modulation of biological processes, interaction with specific molecular targets

Studied properties

Anti-inflammatory and analgesic properties

Promising field

Medicinal chemistry research and development

Check Digit Verification of cas no

The CAS Registry Mumber 89193-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,9 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89193-18:
(7*8)+(6*9)+(5*1)+(4*9)+(3*3)+(2*1)+(1*8)=170
170 % 10 = 0
So 89193-18-0 is a valid CAS Registry Number.

89193-18-0SDS

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 ethyl 3,5-dimethyl-1-phenylpyrazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names Pyrazole carboxylic ester 8

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:89193-18-0 SDS

89193-18-0Relevant articles and documents

WNT SIGNALING PATHWAY INHIBITORS FOR TREATMENTS OF DISEASE

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Paragraph 00277; 00278, (2017/09/15)

Compounds and compositions are provided as inhibitors of the Wnt/β-catenin pathway for the treatment of diseases that implicate the same.

Synthesis of a pyrazol-3-ylidene palladium complex, pyrazolium salts and mesomeric betaines of pyrazole as N-heterocyclic carbene precursors

Dreger, Andrij,Nieger, Martin,Drafz, Martin,Schmidt, Andreas

experimental part, p. 359 - 366 (2012/07/14)

The synthesis of a pyrazol-3-ylidene palladium complex is described, and results of a single-crystal X-ray diffraction study are presented. The properties of pyrazolium salts as well as of two types of heterocyclic mesomeric betaines, the pseudo-cross-con

An effective and general method for the highly regioselective synthesis of 1-phenylpyrazoles from β-enaminoketoesters, tandem Blaise-acylation adducts

Ko, Young Ok,Chun, Yu Sung,Park, Cho-Long,Kim, Youngmee,Shin, Hyunik,Ahn, Sungho,Hong, Jongki,Lee, Sang-Gi

supporting information; experimental part, p. 1132 - 1136 (2009/05/30)

An effective and general route for the regioselective synthesis of 1-phenylpyrazoles has been developed from β-enaminoketoesters prepared by tandem Blaise-acylation. This method is applicable to a very broad range of substrates, generating a diverse set o

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