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Benzenecarboximidic acid, N-(1-oxopropyl)-, methyl ester, also known as methyl N-(1-oxopropyl)benzenecarboximidate, is an organic compound with the chemical formula C11H13NO3. It is a derivative of benzenecarboximidic acid, featuring a methyl ester group attached to the nitrogen atom and a propionyl group (1-oxopropyl) on the nitrogen as well. Benzenecarboximidic acid, N-(1-oxopropyl)-, methyl ester is characterized by its aromatic ring structure, with a carbonyl group (C=O) in the propionyl chain, and an ester group (C-O-C) connecting the benzene ring to the methyl group. It is a colorless to pale yellow liquid and is used in the synthesis of various pharmaceuticals and chemical intermediates due to its reactivity and functional groups.

712-66-3

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712-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 712-66-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 712-66:
(5*7)+(4*1)+(3*2)+(2*6)+(1*6)=63
63 % 10 = 3
So 712-66-3 is a valid CAS Registry Number.

712-66-3SDS

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 methyl N-propanoylbenzenecarboximidate

1.2 Other means of identification

Product number -
Other names Benzenecarboximidic acid,N-(1-oxopropyl)-,methyl ester

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:712-66-3 SDS

712-66-3Relevant academic research and scientific papers

Synthesis of N-(α-Methoxyalkyl) Amides from Imidates

Lokensgard, Jerrold P.,Fischer, John W.,Bartz, William J.

, p. 5609 - 5611 (1985)

Two general routes from imidates to N-(α-methoxyalkyl) amides (e.g.,R'CONHCH(OCH3)R, 1) are reported.The first involves acylation of the imidate on nitrogen with an acyl chloride, followed by reduction with sodium borohydride.In the second, an aldehyde is converted, via its methyl acetal, to an α-chloro methyl ether, which is used to alkylate the imdate.Further treatment with pyridinium chloride in dry Me2SO yields 1.Thirteen examples are reported.

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