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1-(2-NITRO-PHENYL)-AZEPANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40832-88-0

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40832-88-0 Usage

Type of Compound

Heterocyclic organic compound

Nitrogen Content

Contains a nitrogen atom in its seven-membered ring structure

Functional Group

Nitro group (a nitrogen atom bonded to two oxygen atoms)

Industry Usage

Pharmaceutical industry

Application

Synthesis of various drugs and as a building block for the creation of other organic molecules

Potential Applications

Medicinal chemistry, drug discovery research, material science, and organic synthesis

Unique Features

Unique structure and properties that make it useful in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 40832-88-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,3 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40832-88:
(7*4)+(6*0)+(5*8)+(4*3)+(3*2)+(2*8)+(1*8)=110
110 % 10 = 0
So 40832-88-0 is a valid CAS Registry Number.

40832-88-0SDS

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-(2-Nitrophenyl)azepane

1.2 Other means of identification

Product number -
Other names -

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:40832-88-0 SDS

40832-88-0Relevant academic research and scientific papers

Synthesis of benzimidazoles via iridium-catalyzed acceptorless dehydrogenative coupling

Sun, Xiang,Lv, Xiao-Hui,Ye, Lin-Miao,Hu, Yu,Chen, Yan-Yan,Zhang, Xue-Jing,Yan, Ming

supporting information, p. 7381 - 7383 (2015/07/15)

Iridium-catalyzed acceptorless dehydrogenative coupling of tertiary amines and arylamines has been developed. A number of benzimidazoles were prepared in good yields. An iridium-mediated C-H activation mechanism is suggested. This finding represents a novel strategy for the synthesis of benzimidazoles.

Synthesis of benzimidazoles via iridium-catalyzed acceptorless dehydrogenative coupling

Sun, Xiang,Lv, Xiao-Hui,Ye, Lin-Miao,Hu, Yu,Chen, Yan-Yan,Zhang, Xue-Jing,Yan, Ming

supporting information, p. 7381 - 7383 (2015/11/27)

Iridium-catalyzed acceptorless dehydrogenative coupling of tertiary amines and arylamines has been developed. A number of benzimidazoles were prepared in good yields. An iridium-mediated C-H activation mechanism is suggested. This finding represents a novel strategy for the synthesis of benzimidazoles.

Synthesis of new quinoxaline derivatives by reductive cyclization of various 1-(2-nitrophenyl)-2-cyanoamines

Renaud, Tristan,Hurvois, Jean-Pierre,Uriac, Philippe

, p. 987 - 996 (2007/10/03)

The electrochemical cyanation of various six-membered N-(2-nitrophenyl) heterocyclic amines, including piperidine, morpholine, thiomorpholine, and N-Boc-protected piperazine derivatives, was investigated. The expected cyanoamines 5 were obtained in good y

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