75258-07-0

Basic information

• Product Name: 1,2-diacetamido-4-acetoxybenzene
• Synonyms: 1,2-diacetamido-4-acetoxybenzene
• CAS NO: 75258-07-0
• Molecular Weight: 250.254
• Mol File: 75258-07-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-diacetamido-4-acetoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-diacetamido-4-acetoxybenzene(75258-07-0)
• EPA Substance Registry System: 1,2-diacetamido-4-acetoxybenzene(75258-07-0)

Safety Data

• Hazardous Substances Data: 75258-07-0(Hazardous Substances Data)

Upstream product

• 7403-75-0 N-(4-hydroxy-2-nitrophenyl)-acetamide 
• 108-24-7 acetic anhydride 
• 2243-69-8 4-acetamido-3-nitrophenyl acetate 
• 2623-33-8 4-acetoxyacetanilide 
• 610-81-1 4-hydroxy-2-nitroaniline 
• 27992-37-6 1-hydroxy-2,2-dimethyl-4,5,6,7-tetrahydrobenzimidazoline 3-oxide 
• 492-99-9 1,2-cyclohexanedionedioxime 
• 50700-49-7 N-acetyl-p-benzoquinoneimine 
• 103-90-2 4-acetaminophenol 
• 66927-19-3 2,2-dimethyl-4,5,6,7-tetrahydro-2H-benzimidazole 1,3-dioxide 
• 51-17-2 benzoimidazole 
• 546-67-8 lead(IV) tetraacetate 
• 7474-93-3 4-acetamido-3-aminophenyl acetate 

Downstream Products

• 4053-51-4 2-acetylamino-1,4-benzoquinone 
• 75258-08-1 1-hydroxy-3,4-diacetamidobenzene 

Relevant articles and documents

A NEW NITRATION PRODUCT, 3-NITRO-4-ACETAMIDOPHENOL, OBTAINED FROM ACETAMINOPHEN WITH NITROUS ACID

Treatment of acetaminophen with an excess sodium nitrite under mildly acidic to neutral conditions results in smooth formation of new 3-nitro-4-acetamidophenol via N-acetyl-p-benzoquinone imine as an oxidation intermediate, which is a well-known, widely e

PREPARATION AND SOME PROPERTIES OF 2H-IMIDAZOLE 1,3-DIOXIDES, DERIVATIVES OF ALICYCLIC 1,2-DIOXIMES

The corresponding 2H-imidazole 1,3-dioxides were obtained by the reaction of cyclohexanedione and cycloheptanedione 1,2-dioximes with acetone, cyclopentanone, and methyl ethyl ketone.The reactions of these compounds with hydroxylamine hydrochloride, NaBH4, a Grignard reagent, and acetic anhydride in the presence of H2SO4 were studied in the case of 2,2-dimethyl-4,5,6,7-tetrahydro-2H-benzimidazole 1,3-dioxide.Bromination of the latter and 2,2-dimethylcyclohepta-2H-imidazole 1,3-dioxide with N-bromosuccinimide gave the corresponding dibromo derivatives, the bromineatoms in which are replaced by acetoxy and hydroxy groups. 4,7-Dihydroxy-2,2-dimethyl-4,5,6,7-tetrahydro-2H-benzimidazole 1,3-dioxide, which was obtained by oxidation with MnO2, was converted to a quinone, viz., 2,2-dimethyl-4,7-dioxo-4,7-dihydro-2H-benzimidazole 1,3-dioxide.