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92164-25-5

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92164-25-5 Usage

General Description

2-[(phenylthio)methyl]benzonitrile is a chemical compound with the molecular formula C15H11NS. It is a white to off-white crystalline solid that is commonly used in the synthesis of various pharmaceutical and organic compounds. 2-[(phenylthio)methyl]benzonitrile is often used as a reagent in organic synthesis reactions, particularly in the production of heterocyclic compounds and pharmaceutical intermediates. It is also known for its ability to act as a nucleophile and a radical scavenger, making it useful in a wide range of chemical reactions. Additionally, 2-[(phenylthio)methyl]benzonitrile has potential applications in the development of new materials and in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 92164-25-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,6 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92164-25:
(7*9)+(6*2)+(5*1)+(4*6)+(3*4)+(2*2)+(1*5)=125
125 % 10 = 5
So 92164-25-5 is a valid CAS Registry Number.

92164-25-5SDS

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 Benzonitrile, 2-[(phenylthio)methyl]-

1.2 Other means of identification

Product number -
Other names 2-(PHENYLTHIOMETHYL)BENZONITRILE

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:92164-25-5 SDS

92164-25-5Upstream product

92164-25-5Relevant articles and documents

Iodine ate complexes and N-lithiobenzocyclobutenamine intermediates in the reactions of α-lithionitriles with benzyne

Tripathy,Hussain,Durst

, p. 8401 - 8405 (2007/10/03)

α-Lithionitriles add to benzynes to give N-lithiobenzocyclobutenamines in a two-step process. The intermediate aryllithiums can be trapped prior to cyclization with iodobenzene or 2,6-dimethoxyiodobenzene to form iodine-ate complex intermediates which fragment preferentially to 2-(α-cyanobenzyl)-iodobenzenes. The N-lithiobenzocyclobutenamines undergo ring opening to yield either 2-substituted benzonitriles or α-substituted benzylcyanides depending on the substitution pattern on the aryl and cyclobutene rings. (C) 2000 Published by Elsevier Science Ltd.

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