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709-04-6

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709-04-6 Usage

General Description

1-Phenyl-1H-pyrazole-4-carbonitrile is an organic compound with the molecular formula C11H7N3. It is a pyrazole derivative that contains a phenyl group and a carbonitrile group. 1-Phenyl-1H-pyrazole-4-carbonitrile has potential applications in the field of medicinal chemistry, and it may be used as a building block for the synthesis of biologically active compounds. Its structure and properties make it a valuable intermediate for the production of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, its unique chemical properties and reactivity make it a valuable tool for research and development in the field of organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 709-04-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 709-04:
(5*7)+(4*0)+(3*9)+(2*0)+(1*4)=66
66 % 10 = 6
So 709-04-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H7N3/c11-6-9-7-12-13(8-9)10-4-2-1-3-5-10/h1-5,7-8H

709-04-6 Well-known Company Product Price

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  • Aldrich

  • (JRD0249)  4-Cyano-1-phenylpyrazole  AldrichCPR

  • 709-04-6

  • JRD0249-1G

  • 2,901.60CNY

  • Detail

709-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenylpyrazole-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 1-Phenyl-1H-pyrazol-4-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:709-04-6 SDS

709-04-6Relevant articles and documents

Synergistic Indium and Silver Dual Catalysis: A Regioselective [2 + 2 + 1]-Oxidative N-Annulation Approach for the Diverse and Polyfunctionalized N-Arylpyrazoles

Thombal, Raju S.,Lee, Yong Rok

, p. 4681 - 4685 (2018)

Indium(III)/silver(I)-catalyzed [2 + 2 + 1] annulation of arylhydrazine hydrochlorides with β-enamino esters via multicomponent reactions for the construction of diverse and multisubstituted N-arylpyrazoles has been demonstrated. The oxidative cycloaddition proceeds via a cascade triple Michael addition/elimination/air oxidation. This novel protocol provides a rapid and efficient synthetic route to various 3,4-diester-substituted N-arylpyrazoles. The synthesized compounds are further utilized for various synthetic transformations.

Synthesis of pyrazole-carboxamides and pyrazole-carboxylic acids derivatives: Simple methods to access powerful building blocks

Dos Santos, Maurício Silva,Ferreira, Byanca Silva,Silva, Rafaela Corrêa,Souto, Bernardo Araújo

, p. 335 - 343 (2021/09/07)

Hybrid systems containing pyrazole moiety show a wide spectrum of biological activities. To access novel hybrids with pyrazole ring, in this work we synthesized twenty pyrazole-carboxylic acids and twenty pyrazole-carboxamides, using simple synthetic methods, to be used as building blocks in the development of new structures.

A Convenient Synthesis of Pyrazole-imidazoline Derivatives by Microwave Irradiation

de S. Rosa, Getúlio,Souto, Bernardo A.,Pereira, Cynthia N.,Teixeira, Bruna C.,dos Santos, Maurício S.

, p. 1825 - 1830 (2019/04/30)

A series of 28 hybrids pyrazole-imidazolines 1a–n and 2a–n were synthesized by a new methodology using microwave irradiation, in short time (20–30?min), in low power (50–70?W), and in 34–92% yield. Among all methodologies evaluated, no side products were obtained. All derivatives were completely characterized by FT–IR, 1H and 13C NMR, GC–MS, and HRMS.

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