6335-42-8 Usage
Description
2-Hydroxyimino-N-(2-methoxyphenyl)acetamide is a chemical compound with the molecular formula C10H12N2O3. It is a derivative of acetamide with a hydroxyimino group and a methoxyphenyl group attached to the nitrogen atom. 2-HYDROXYIMINO-N-(2-METHOXY-PHENYL)-ACETAMIDE has the potential to act as an inhibitor of enzymes such as matrix metalloproteinases and the angiotensin-converting enzyme, making it significant in the field of medicinal chemistry.
Uses
Used in Pharmaceutical Industry:
2-Hydroxyimino-N-(2-methoxyphenyl)acetamide is used as a potential enzyme inhibitor for [application reason], such as inhibiting matrix metalloproteinases and the angiotensin-converting enzyme. Its ability to inhibit these enzymes may contribute to the development of pharmaceuticals for various therapeutic purposes.
Further research and testing are required to fully understand the potential uses and effects of 2-Hydroxyimino-N-(2-methoxyphenyl)acetamide in different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6335-42-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6335-42:
(6*6)+(5*3)+(4*3)+(3*5)+(2*4)+(1*2)=88
88 % 10 = 8
So 6335-42-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O3/c1-14-8-5-3-2-4-7(8)11-9(12)6-10-13/h2-6,13H,1H3,(H,11,12)/b10-6+
6335-42-8Relevant articles and documents
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.