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(2E)-N-(5-CHLORO-2-METHOXYPHENYL)-2-(HYDROXYIMINO)ACETAMIDE, also known as Cl-V-Pyrrolidin-6-ylidene-5-methoxy-4-hydroxybenzamide, is a chemical compound with the molecular formula C11H11ClN2O3. It is a derivative of acetamide and contains a chloro, methoxy, and hydroxyimino group. (2E)-N-(5-CHLORO-2-METHOXYPHENYL)-2-(HYDROXYIMINO)ACETAMIDE is commonly used in pharmaceutical research and development due to its potential medicinal properties.

67303-24-6

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67303-24-6 Usage

Uses

Used in Pharmaceutical Research and Development:
(2E)-N-(5-CHLORO-2-METHOXYPHENYL)-2-(HYDROXYIMINO)ACETAMIDE is used as a chemical compound in pharmaceutical research and development for its potential medicinal properties. The specific uses and applications of (2E)-N-(5-CHLORO-2-METHOXYPHENYL)-2-(HYDROXYIMINO)ACETAMIDE may vary depending on the context and the specific goals of a given research or development project.

Check Digit Verification of cas no

The CAS Registry Mumber 67303-24-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,0 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67303-24:
(7*6)+(6*7)+(5*3)+(4*0)+(3*3)+(2*2)+(1*4)=116
116 % 10 = 6
So 67303-24-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClN2O3/c1-15-8-3-2-6(10)4-7(8)12-9(13)5-11-14/h2-5,14H,1H3,(H,12,13)/b11-5-

67303-24-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E)-N-(5-Chloro-2-methoxyphenyl)-2-(hydroxyimino)acetamide

1.2 Other means of identification

Product number -
Other names -

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

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More Details:67303-24-6 SDS

67303-24-6Relevant academic research and scientific papers

An improved synthesis of isonitrosoacetanilides

Rewcastle, Gordon W.,Sutherland, Hamish S.,Weir, Claudette A.,Blackburn, Adrian G.,Denny, William A.

, p. 8719 - 8721 (2007/10/03)

A novel two-step synthesis of isonitrosoacetanilides [2-(hydroxyimino)-N- phenylacetamides] has been developed, involving the initial acylation of aniline derivatives with 2,2-diacetoxyacetyl chloride, followed by reaction with hydroxylamine hydrochloride. The method works equally well with a variety of different aniline derivatives, including those with poor aqueous solubility and those containing electron rich ortho-substituents, neither of which react well under traditional conditions.

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