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3,5-DIMETHYL-1-PHENYL-1H-PYRAZOLE-4-CARBONITRILE, with the molecular formula C12H11N3, is a pyrazole derivative that is widely used in organic synthesis and pharmaceutical research. It is an important intermediate in the production of various pharmaceuticals and agrochemicals, and has been studied for its potential biological activities, including anti-inflammatory and antitumor properties. Known for its stability and versatility in chemical reactions, it serves as a valuable building block for the synthesis of diverse compounds.

23198-55-2

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23198-55-2 Usage

Uses

Used in Pharmaceutical Industry:
3,5-DIMETHYL-1-PHENYL-1H-PYRAZOLE-4-CARBONITRILE is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
3,5-DIMETHYL-1-PHENYL-1H-PYRAZOLE-4-CARBONITRILE is used as an intermediate in the production of agrochemicals to help create effective compounds for agricultural applications, such as pesticides and herbicides.
Used in Organic Synthesis:
3,5-DIMETHYL-1-PHENYL-1H-PYRAZOLE-4-CARBONITRILE is used as a building block in organic synthesis for its stability and versatility, allowing for the creation of a wide range of chemical compounds with various applications.
Used in Biological Research:
3,5-DIMETHYL-1-PHENYL-1H-PYRAZOLE-4-CARBONITRILE is used in biological research for its potential anti-inflammatory and antitumor properties, contributing to the study and development of new treatments for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 23198-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,9 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23198-55:
(7*2)+(6*3)+(5*1)+(4*9)+(3*8)+(2*5)+(1*5)=112
112 % 10 = 2
So 23198-55-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H11N3/c1-9-12(8-13)10(2)15(14-9)11-6-4-3-5-7-11/h3-7H,1-2H3

23198-55-2SDS

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 3,5-dimethyl-1-phenylpyrazole-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 3.5-Dimethyl-1-phenyl-pyrazol-4-carbonsaeure-nitril

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:23198-55-2 SDS

23198-55-2Downstream Products

23198-55-2Relevant academic research and scientific papers

A short and expeditious regiospecific synthesis of novel pyrazoles

Chowdhury, S. K. Dutta,Sarkar, Mili,Mahalanabis, Kumar K.

, p. 746 - 748 (2007/10/03)

α-Cyano-β-enaminones, obtained by regioselective acylation of β-aminocrotononitrile, are smoothly and regiospecifically converted into substituted pyrazoles in good to excellent yields.

NEW FUNCTIONALIZED PYRAZOLES FROM ISOXAZOLOPYRIDAZINONES

Piaz, Vittorio Dal,Ciciani, Giovanna,Chimichi, Stefano

, p. 365 - 369 (2007/10/02)

Treatment of 3-methylisoxazolopyridazin-7(6H)-ones (1a-d) with dilute NaOH affords in good yields new pyrazole derivatives which can be regarded as building blocks for condensed heterocycles with potential biological activity.

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