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N-hydroxy-N-(4-methylphenyl)formamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73747-07-6

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73747-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73747-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,4 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73747-07:
(7*7)+(6*3)+(5*7)+(4*4)+(3*7)+(2*0)+(1*7)=146
146 % 10 = 6
So 73747-07-6 is a valid CAS Registry Number.

73747-07-6SDS

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-hydroxy-N-(4-methylphenyl)formamide

1.2 Other means of identification

Product number -
Other names N-p-Tolylformohydroxamsaeure

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:73747-07-6 SDS

73747-07-6Relevant academic research and scientific papers

A facile synthesis of N-aryl-N-hydroxyformamides from N-arylhydroxylamines

Ayyangar, N. R.,Brahme, K. C.,Shingare, M. S.,Srinivasan, K. V.

, p. 961 - 963 (2007/10/02)

Several N-arylhydroxylamines (2) have been formylated for the first time with acetic formic anhydride to yield N-hydroxyformanilides (3) in better yields than hitherto reported.

Reactions of N1-Hydroxyformamidines with Heterocumulenes

Zinner, Gerwalt,Schecker, Heinz-Guenther,Heuer, Wilhelm

, p. 1006 - 1014 (2007/10/02)

N1-Hydroxyformamidines and isocyanates react to yield N1-(carbamoyloxy)formamidines and/or 3-amino-1,2,4-oxazolidin-5-ones.Frequently the formation of ureas is observed.It can be explained by an oxidoreductive rearrangement to 1,3,5-trisubstituted biurets which undergo abstraction of isocyanate.Reactions with carbodiimides lead to 3-amino-5-imino-1,2,4-oxadiazolidines, ureas and carbodiimides not identical with the educts.

Reaction of Nitroso Aromatics with Glyoxylic Acid. A New Path to Hydroxamic Acids

Corbett, Michael D.,Corbett, Bernadette R.

, p. 2834 - 2839 (2007/10/02)

In aqueous solution substituted aromatic nitroso compounds react rapidly with glyoxylic acid to produce N-hydroxyformanilides and CO2.The reaction is nearly quantitative for all nitroso aromatics investigated and serves as a convenient synthetic route to

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