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Benzenamine, 2-cyclooctyl-, also known as 2-cyclooctylaniline or 2-(cyclooctylamino)benzene, is an organic compound with the chemical formula C16H23N. It is a derivative of aniline, where a cyclooctyl group replaces one of the hydrogen atoms on the nitrogen atom. Benzenamine, 2-cyclooctyl- is characterized by its aromatic structure and the presence of a cyclooctane ring, which contributes to its unique chemical properties. Benzenamine, 2-cyclooctyl-, is used in various applications, including the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its physical properties include a melting point of 40-42°C and a boiling point of approximately 360°C. Due to its potential reactivity and the presence of both aromatic and amine functional groups, it is important to handle Benzenamine, 2-cyclooctyl- with care, following appropriate safety guidelines.

4806-78-4

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4806-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4806-78-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,0 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4806-78:
(6*4)+(5*8)+(4*0)+(3*6)+(2*7)+(1*8)=104
104 % 10 = 4
So 4806-78-4 is a valid CAS Registry Number.

4806-78-4SDS

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 2-cyclooctylaniline

1.2 Other means of identification

Product number -
Other names o-Cyclooctyl-anilin

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:4806-78-4 SDS

4806-78-4Relevant academic research and scientific papers

Selective Acid-Catalyzed Hydroarylation of Nonactivated Alkenes with Aniline Assisted by Hexafluoroisopropanol

De Oliveira Vigier, Karine,Humblot, Anaelle,Jér?me, Fran?ois,Jiang, Fan,Peng, Gongming,Pera-Titus, Marc,Wischert, Raphael

, p. 17896 - 17905 (2021/12/13)

The catalytic hydroarylation of nonactivated alkenes with aniline is a reaction of high interest, aiming at providing C-functionalized aniline derivatives that are important precursors for the fabrication of polyurethanes. However, this reaction remains a

Proton-catalyzed hydroamination and hydroarylation reactions of anilines and alkenes: A dramatic effect of counteranions on reaction efficiency

Anderson, Laura L.,Arnold, John,Bergman, Robert G.

, p. 14542 - 14543 (2007/10/03)

The anilinium salt, [PhNH3][B(C6F5)4], has been identified as a catalyst for the hydroamination and hydroarylation of several different types of alkenes with anilines. The weakly coordinating counterion of this

Design of arylimine postmetallocene catalytic systems for olefin polymerization: I. Synthesis of substituted 2-cycloalkyl- and 2,6-dicycloalkylanilines

Oleinik,Oleinik,Abdrakhmanov,Ivanchev,Tolstikov

, p. 1423 - 1427 (2007/10/03)

A convenient synthetic approach to substituted 2-cycloalkyl- and 2,6-dicycloalkylanilines, involving catalytic hydrogenation on Raney nickel in methanol of readily available o-cycloalkenylanilines prepared by reaction of cyclic alkyl halides with anilines

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