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1-p-tolyl-1H-pyrazole-4-carbonitrile is a pyrazole derivative chemical compound characterized by the molecular formula C11H8N4. It features a p-tolyl group and a carbonitrile functional group, presenting as a crystalline solid with a high melting point and limited solubility in water. 1-p-tolyl-1H-pyrazole-4-carbonitrile is recognized for its role as an intermediate in the synthesis of pharmaceuticals and agrochemicals, holding potential for the development of novel drugs and agrochemical products. Due to its potential hazards, it is crucial to handle 1-p-tolyl-1H-pyrazole-4-carbonitrile with appropriate safety measures and precautions.

712-72-1

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712-72-1 Usage

Uses

Used in Pharmaceutical Industry:
1-p-tolyl-1H-pyrazole-4-carbonitrile is used as a synthetic intermediate for the development of new pharmaceutical compounds. Its unique structure allows for the creation of a variety of drug candidates that can target specific biological pathways or receptors, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 1-p-tolyl-1H-pyrazole-4-carbonitrile serves as a key intermediate in the synthesis of agrochemicals. It is utilized to develop new pesticides, herbicides, or other crop protection agents that can effectively manage agricultural pests and diseases, thereby enhancing crop yield and quality.
Given the compound's potential applications and the need for safety, it is imperative that researchers and manufacturers adhere to strict protocols during its synthesis, handling, and application to ensure both environmental and human safety.

Check Digit Verification of cas no

The CAS Registry Mumber 712-72-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 712-72:
(5*7)+(4*1)+(3*2)+(2*7)+(1*2)=61
61 % 10 = 1
So 712-72-1 is a valid CAS Registry Number.

712-72-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methylphenyl)pyrazole-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 1-p-tolyl-1H-pyrazole-4-carbonitrile

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:712-72-1 SDS

712-72-1Downstream Products

712-72-1Relevant academic research and scientific papers

Unveiling Potent Photooxidation Behavior of Catalytic Photoreductants

Targos, Karina,Williams, Oliver P.,Wickens, Zachary K.

supporting information, p. 4125 - 4132 (2021/04/07)

We describe a photocatalytic system that reveals latent photooxidant behavior from one of the most reducing conventional photoredox catalysts, N-phenylphenothiazine (PTH). This aerobic photochemical reaction engages difficult to oxidize feedstocks, such as benzene, in C(sp2)-N coupling reactions through direct oxidation. Mechanistic studies are consistent with activation of PTH via photooxidation and with Lewis acid cocatalysts scavenging inhibitors inextricably formed in this process.

Cyanoacetaldehyde - New Synthetic Applications of an Old Compound Syntheses with Nitriles, XCI

Jachak, Madhukar,Kriessmann, Ulrike,Mittelbach, Martin,Junek, Hans

, p. 199 - 208 (2007/10/02)

Various reactions of cyanoacetaldehyde (1), freshly prepared by ozonization of (E)-1,4-dicyano-2-butene or allylcyanide, are described.Thus, conversion of 1 with anilines gave β-phenylaminoacrylonitriles 2a-e.Reaction of 1 with hydrazines led to the corresponding hydrazones 3a-e, which could be cyclized under alkaline conditions to 5-aminopyrazoles 4a-d.An aldol-type condensation product 5a could be obtained by reaction of 1 with sodiumphenoxide.Treatment of 1 with dimethylformamide-dimethylacetal led to the formation of (E)-3-dimethylamino-2-formylpropenenitrile (6), a very useful synthon in synthetic chemistry.For the determination of the structure of 6 the method of steady state diffferential NOEs was used.Reaction of 6 with hydrazines gave 1-substituted-4-cyanopyrazoles 7a-k. Keywords.Cyanoacetaldehyde; Hydrazones; Cyanopyrazoles; Aminopyrazoles.

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