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22192-84-3

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22192-84-3 Usage

General Description

N-CYANOMETHYL-4-METHOXY-BENZAMIDE is a chemical compound that belongs to the group of benzamides, which are aromatic compounds containing a benzene ring with an amide functional group attached. This specific compound has a nitrile (cyano) group attached to the carbon next to the amide, as well as a methoxy group attached to the benzene ring. It is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. This chemical may have potential applications in the development of drugs and other products due to its versatile nature and functional groups. Additionally, it is important to handle this compound with care and adhere to proper safety measures when working with it in a laboratory or industrial setting.

Check Digit Verification of cas no

The CAS Registry Mumber 22192-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,9 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22192-84:
(7*2)+(6*2)+(5*1)+(4*9)+(3*2)+(2*8)+(1*4)=93
93 % 10 = 3
So 22192-84-3 is a valid CAS Registry Number.

22192-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(Cyanomethyl)-4-methoxybenzamide

1.2 Other means of identification

Product number -
Other names 4-Methoxy-benzaminoacetonitril

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:22192-84-3 SDS

22192-84-3Downstream Products

22192-84-3Relevant articles and documents

Synthesis of Imidazoles and Oxazoles via a Palladium-Catalyzed Decarboxylative Addition/Cyclization Reaction Sequence of Aromatic Carboxylic Acids with Functionalized Aliphatic Nitriles

Dai, Ling,Yu, Shuling,Lv, Ningning,Ye, Xuanzeng,Shao, Yinlin,Chen, Zhongyan,Chen, Jiuxi

supporting information, p. 5664 - 5668 (2021/08/01)

We herein report an efficient approach for the assembly of multiply substituted imidazoles and oxazoles in a single-step manner. These transformations are based on a decarboxylation addition and annulation of readily accessible aromatic carboxylic acids a

Syntheses of 2-acylaminoacetamidine and 3-acylaminopropionamidine derivatives.

Ueda,Okamoto,Tsuji,Muraoka

, p. 2355 - 2361 (2007/10/06)

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