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24652-31-1

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24652-31-1 Usage

Pyrazole derivative

A class of organic compounds containing a five-membered heterocyclic ring with two nitrogen atoms This compound belongs to the pyrazole family, which is known for its various applications in organic synthesis and pharmaceutical research.

Carbonitrile group

A cyano group (C≡N) attached to the pyrazole ring The presence of this group contributes to the compound's unique reactivity and potential applications in organic synthesis.

1,3-Diphenyl substitution

Two phenyl groups (C6H5) are attached to the first and third positions of the pyrazole ring This substitution pattern influences the compound's physical and chemical properties, as well as its potential applications.

Organic synthesis applications

The compound may be used as a building block or intermediate in the synthesis of more complex organic molecules Due to its unique structure, 1H-Pyrazole-5-carbonitrile, 1,3-diphenylcould be valuable in creating new organic compounds.

Pharmaceutical research potential

The compound's structure and properties may make it a candidate for drug development or as a pharmaceutical intermediate Further research and testing are needed to determine its specific uses in the pharmaceutical industry.

Further research and testing required

To fully assess the compound's potential and specific uses in various industries, additional studies and experiments must be conducted The compound's unique structure warrants further investigation to explore its possible applications and benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 24652-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,5 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24652-31:
(7*2)+(6*4)+(5*6)+(4*5)+(3*2)+(2*3)+(1*1)=101
101 % 10 = 1
So 24652-31-1 is a valid CAS Registry Number.

24652-31-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-diphenyl-1H-pyrazole-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 1,3-Diphenylpyrazol-5-carbonitril

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:24652-31-1 SDS

24652-31-1Relevant articles and documents

Iron nitrate/TEMPO: A superior homogeneous catalyst for oxidation of primary alcohols to nitriles in air

Dighe, Shashikant U.,Chowdhury, Deepan,Batra, Sanjay

, p. 3892 - 3896 (2015/01/09)

A highly practical, one-step, facile synthesis of aromatic, heteroaromatic, allylic and aliphatic nitriles from primary alcohols catalyzed by ferric nitrate [Fe(NO3)3·9H2O] in the presence of TEMPO, aqueous ammonia and air at room temperature is described.

A ONE STEP SYNTHESIS OF 4-CYANOPYRAZOLES

Hassaneen, Hamdi M.,Ead, Hamed A.,Elwan, Nehal M.,Shawali, Ahmed S.

, p. 2857 - 2862 (2007/10/02)

Reaction of nitrilimines 2 with fumaronitrile 6 yielded 4-cyanopyrazoles 8 in good yields.The structures of 8 were substantiated by comparison with their regioisomers 5-cyanopyrazoles 5, prepared by addition of 2 to acrylonitrile followed by oxidation of

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