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Benzenamine, N-methylene-, N-oxide, also known as N-Methylen-N-oxid-anilin or N-Methylen-N-oxid-benzylamin, is a chemical compound with the molecular formula C7H8NO. It is an organic compound derived from benzenamine (aniline), where a methylene group (-CH2-) is attached to the nitrogen atom, and an oxide group (-O) is present on the nitrogen as well. Benzenamine, N-methylene-, N-oxide is often used as an intermediate in the synthesis of various pharmaceuticals, dyes, and other organic compounds. It is typically synthesized through the oxidation of N-methylen-aniline, and its properties include a melting point of around 105-107°C. Due to its reactivity, it is important to handle Benzenamine, N-methylene-, N-oxide with care, following proper safety protocols.

4745-47-5

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4745-47-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4745-47-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,4 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4745-47:
(6*4)+(5*7)+(4*4)+(3*5)+(2*4)+(1*7)=105
105 % 10 = 5
So 4745-47-5 is a valid CAS Registry Number.

4745-47-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenylmethanimine oxide

1.2 Other means of identification

Product number -
Other names Benzenamine,N-methylene-,N-oxide

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:4745-47-5 SDS

4745-47-5Relevant academic research and scientific papers

Annelation of Cyclic Dienes to Amino- and Azabicyclic Diols by Iterated Cycloadditions of Nitrones

Bailey, J. T.,Berger, I.,Friary, R.,Puar, M. S.

, p. 857 - 863 (1982)

Bimolecular cycloadditions of nitrones to cyclic dienes, followed by MCPBA N-oxidations of the resulting unsaturated isoxazolidines, intramolecular cycloadditions of the derived nitrones, and hydrogenolyses of the corresponding tricyclic isoxazolidines, a

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