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Benzenemethanamine, N-(4-methoxyphenyl)-N-nitroso-, also known as 4-methoxyphenyl-N-nitroso-N-phenylamine, is an organic compound with the chemical formula C13H12N2O2. It is a derivative of benzenemethanamine, featuring a nitroso group (-N=O) and a 4-methoxyphenyl group attached to the nitrogen atom. Benzenemethanamine, N-(4-methoxyphenyl)-N-nitroso- is characterized by its yellow crystalline appearance and is soluble in organic solvents. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. Due to its potential reactivity and the presence of a nitroso group, it is important to handle Benzenemethanamine, N-(4-methoxyphenyl)-N-nitroso- with care, following appropriate safety guidelines.

5705-13-5

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5705-13-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5705-13-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,0 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5705-13:
(6*5)+(5*7)+(4*0)+(3*5)+(2*1)+(1*3)=85
85 % 10 = 5
So 5705-13-5 is a valid CAS Registry Number.

5705-13-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(4-chlorophenyl)-2-oxoethyl]sulfanyl-3-cyclohexylspiro[6H-benzo[h]quinazoline-5,1'-cyclohexane]-4-one

1.2 Other means of identification

Product number -
Other names N-Benzyl-N-nitroso-p-anisidin

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:5705-13-5 SDS

5705-13-5Downstream Products

5705-13-5Relevant academic research and scientific papers

Regioselective Nitration of N-Alkyl Anilines using tert-Butyl Nitrite under Mild Condition

Chaudhary, Priyanka,Gupta, Surabhi,Muniyappan, Nalluchamy,Sabiah, Shahulhameed,Kandasamy, Jeyakumar

, p. 104 - 119 (2019/01/08)

Regioselective ring nitration of N-alkyl anilines is reported using tert-butyl nitrite. The reactions proceed efficiently with a wide range of substrates providing synthetically useful N-nitroso N-alkyl nitroanilines in excellent yields which can be easily converted into N-alkyl phenylenediamines and N-alkyl nitroanilines using Zn-AcOH and HCl/MeOH, respectively.

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