6596-66-3

Basic information

• Product Name: 4-[(2,2-dimethylbutanoyl)amino]benzamide
• Synonyms: benzamide, 4-[(2,2-dimethyl-1-oxobutyl)amino]-
• CAS NO: 6596-66-3
• Molecular Formula: C₁₄H₁₄N₂O
• Molecular Weight: 234.2942
• Mol File: 6596-66-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 450.3°C at 760 mmHg
• Flash Point: 226.1°C
• Density: 1.13g/cm³
• Vapor Pressure: 2.67E-08mmHg at 25°C
• Refractive Index: 1.569
• CAS DataBase Reference: 4-[(2,2-dimethylbutanoyl)amino]benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[(2,2-dimethylbutanoyl)amino]benzamide(6596-66-3)
• EPA Substance Registry System: 4-[(2,2-dimethylbutanoyl)amino]benzamide(6596-66-3)

Safety Data

• Hazardous Substances Data: 6596-66-3(Hazardous Substances Data)

Upstream product

• 857815-07-7 N-chloroacetyl-N-phenyl-N'-phenylacetyl-hydrazine 
• 103-81-1 Benzeneacetamide 
• 100-63-0 phenylhydrazine 
• 103-82-2 phenylacetic acid 
• 103-80-0 phenylacetyl chloride 
• 412019-21-7 ethyl 2-acetyl-3-oxo-4-phenylbutanoate 
• 60-29-7 diethyl ether 
• 67-64-1 acetone 
• 72358-76-0 phenylhydrazine acetate 
• 174282-49-6 trifluoro-N-(2-phenylacetyl)methanesulfonamide 

Downstream Products

• 113136-13-3 phenyl-acetic acid-(N'-benzylidene-N-phenyl-hydrazide) 
• 857815-07-7 N-chloroacetyl-N-phenyl-N'-phenylacetyl-hydrazine 
• 34546-90-2 5-benzyl-3-phenyl-3H-[1,3,4]oxadiazol-2-one 
• 3214-06-0 5-benzyl-2-phenyl-1,2-dihydro-[1,2,4]triazol-3-one 
• 52023-40-2 phenyl-acetic acid-(N',N'-diphenyl-hydrazide) 
• 3456-79-9 3-phenyloxindole 
• 92521-93-2 1-phenylacetyl-2-phenyl-5-hydroxypyrazolidine 
• 16537-09-0 t-butyl phenylacetate 

Relevant articles and documents

A formal [3+2] cycloaddition reaction of: N -methylimidazole as a masked hydrogen cyanide: Access to 1,3-disubstitued-1 H -1,2,4-triazoles

N-Methylimidazole (NMI) can act as a masked HCN in the synthesis of 1,3-disubstitued-1H-1,2,4-triazoles via a formal cycloaddition reaction of hydrazonoyl chloride with NMI. The product was proved to be formed via an initial nucleophilic substitution of hydrazonoyl chloride with NMI following cyclization and two sequential C-N bond cleavages. This journal is

Reactions of N-sulfinyltrifluoromethanesulfonamide with carboxylic acids

Phenylacetic, diphenylacetic, salicylic, and cinnamic acids reacted with N-sulfinyltrifluoromethanesulfonamide (CF3SO2NSO) to give the corresponding N-acyltrifluoromethanesulfonamides CF3SO 2NHCOR (R = PhCH

Syntheses of hydrazides by a direct condensation reaction using phosphorous acid-iodine as a reagent

Aliphatic and aromatic hydrazides have been prepared in high to moderate yields by a direct condensation reaction of aliphatic or aromatic carboxylic acids with hydrazine or phenylhydrazine using phosphorous acid-iodine as reagent and pyridine as base and solvent. With aliphatic carboxylic acids, we obtained good results heating at 80-90°, for 5-6 hours, but with aromatic carboxylic acids are necessary 140-150°, for the same period of time.