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N-Nitroso-N-cyclohexylaniline is a chemical compound belonging to the N-nitrosamines class, characterized by the presence of a cyclohexyl and aniline group with a nitroso group attached to the nitrogen atom. It is recognized as a potential human carcinogen due to its mutagenic and carcinogenic properties.

54955-24-7

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54955-24-7 Usage

Uses

Used in Rubber Industry:
N-Nitroso-N-cyclohexylaniline is used as a rubber antioxidant and antiozonant additive to enhance the durability and lifespan of rubber products by preventing degradation. However, due to its health risks, its use has been restricted or banned in certain countries.

Check Digit Verification of cas no

The CAS Registry Mumber 54955-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,5 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54955-24:
(7*5)+(6*4)+(5*9)+(4*5)+(3*5)+(2*2)+(1*4)=147
147 % 10 = 7
So 54955-24-7 is a valid CAS Registry Number.

54955-24-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-cyclohexyl-N-phenylnitrous amide

1.2 Other means of identification

Product number -
Other names Benzenamine,N-cyclohexyl-N-nitroso

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:54955-24-7 SDS

54955-24-7Relevant academic research and scientific papers

Rhodium(iii)-catalyzed indole synthesis at room temperature using the transient oxidizing directing group strategy

Shang, Yaping,Jonnada, Krishna,Yedage, Subhash Laxman,Tu, Hua,Zhang, Xiaofeng,Lou, Xin,Huang, Shijun,Su, Weiping

supporting information, p. 9547 - 9550 (2019/08/15)

Rh-catalyzed reactions of N-alkyl anilines with internal alkynes at room temperature have been developed using an in situ generated N-nitroso group as a transient oxidizing directing group. Due to mild reaction conditions, this method enabled synthesis of a broad range of N-alkyl indoles, including even two indole-based medicinal compounds. Our work disclosed the feasibility of the transient oxidizing directing group strategy in C-H functionalization reactions, which possesses the potential to enhance overall step-economy and impart new reactivity patterns to substrates.

Efficient procedure for chemoselective N-nitrosation of secondary amines with trichloromelamine-NaNO2

Bamoniri,Zolfigol,Mirjalili,Fallah

, p. 1393 - 1396 (2008/03/27)

A combination of trichloromelamine and sodium nitrite in the presence of wet silica gel was used as an effective nitrosating agent for the transformation of secondary amines into the corresponding N-nitroso derivatives under mild and heterogeneous conditions in good to excellent yields.

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