7340-09-2

Basic information

• Product Name: acetamido acetate
• Synonyms: acetamido acetate;N,O-Diacetylhydroxylamine;N-Acetyloxyacetamide;O2-Acetylacetohydroximic acid
• CAS NO: 7340-09-2
• Molecular Formula: C₄H₇NO₃
• Molecular Weight: 117.1
• Mol File: 7340-09-2.mol
• Article Data: 3

Chemical Properties

• Melting Point: 90 °C
• Appearance: /
• Density: 1.126g/cm³
• Refractive Index: 1.413
• CAS DataBase Reference: acetamido acetate(CAS DataBase Reference)
• NIST Chemistry Reference: acetamido acetate(7340-09-2)
• EPA Substance Registry System: acetamido acetate(7340-09-2)

Safety Data

• Hazardous Substances Data: 7340-09-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C4H7NO3/c1-3(6)5-8-4(2)7/h1-2H3,(H,5,6)

Upstream product

• 41879-86-1 acetohydroxamate anion 
• 830-03-5 4-nitrophenol acetate 
• 546-88-3 acetylhydroxamic acid 
• 382165-80-2 N-nitrosodiphenylamine 
• 3451-88-5 1,1'-Diacetyl-1,1',4,4'-tetrahydro-4,4'-bipyridine 
• 614-00-6 N-methyl-N-nitrosoaniline 
• 75-36-5 acetyl chloride 

Downstream Products

• 546-88-3 acetylhydroxamic acid 
• 64-19-7 acetic acid 
• 93-26-5 2-methoxyacetanilide 
• 51-66-1 4-methoxyacetanilide 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 103-89-9 4-Methylacetanilide 
• 1012057-93-0 N-acetoxy-N-(6-(4-(3-chloro-4-fluorophenylamino)-7-methoxyquinazolin-6-yloxy)hexyl)acetamide 
• 87842-89-5 N,O-diacetyl-N-(cyclohexenylmethyl)hydroxylamine 

Relevant articles and documents

The α-effect in micelles: Nucleophilic substitution reaction of p-nitrophenyl acetate with N-phenylbenzohydroxamate ion

Pseudo-first-order rate constants have been determined for the nucleophilic substitution reactions of p-nitrophenyl acetate with p-chlorophenoxide (4-ClC6H4O-) and N-phenylbenzohydroxamate (C6H5CON(C

NAD(P)H and Acetyl-CoA Models: Part II - Reaction of Diphenylnitrosamine and Methylphenylnitrosamine with 1,1'-Diacetyl-1,1',4,4'-tetrahydro-4,4'-bipyridine

Diphenylnitrosamine (1a) and methylphenylnitrosamine (1b) have been treated with 1,1'-diacetyl-1,1',4,4'-tetrahydro-4,4'-bipyridine (DTB) to understand the pattern arising as a result of biomimetic transfer of hydride and acetyl cation from the reagent.A number of products have been isolated and characterized.The interesting feature of the reaction is the -N-N=O cleavage in 1 to give hydroxylamine derivative, O-acetylacetohydroxamic acid (5).