2011-57-6

Basic information

• Product Name: N-(4-hydroxy-2,3-dimethyl-phenyl)acetamide
• Synonyms: N-(4-hydroxy-2,3-dimethyl-phenyl)acetamide
• CAS NO: 2011-57-6
• Molecular Weight: 179.219
• Mol File: 2011-57-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(4-hydroxy-2,3-dimethyl-phenyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-hydroxy-2,3-dimethyl-phenyl)acetamide(2011-57-6)
• EPA Substance Registry System: N-(4-hydroxy-2,3-dimethyl-phenyl)acetamide(2011-57-6)

Safety Data

• Hazardous Substances Data: 2011-57-6(Hazardous Substances Data)

Upstream product

• 74783-54-3 1-hydroxy-2,3-dimethyl-4-nitrosobenzene 
• 108-24-7 acetic anhydride 
• 684201-97-6 4-Sulfobenzolazo-acetoacetaldehyd 
• 78-93-3 butanone 
• 121-57-3 4-aminobenzene sulfonic acid 
• 94276-04-7 4-amino-2,3-dimethyl-1-hydroxybenzene hydrochloride 
• 526-75-0 2,3-Dimethylphenol 
• 3096-69-3 4-amino-2,3-dimethylphenol 
• 153782-51-5 4-(t-butyldimethylsilyloxy)-2,3-dimethylacetanilide 

Downstream Products

• 142874-37-1 4-Acetylamino-2,3-dimethyl-1-(2-methyl-2-propenyloxy)benzene 
• 142902-33-8 4-Acetylamino-2,3-dimethyl-6-(2-methyl-2-propenyl)phenol 
• 179067-16-4 4-methoxy-2,3-dimethylaniline hydrochloride 
• 114747-32-9 N-(4-methoxy-2,3-dimethylphenyl)aniline 
• 74783-55-4 4-acetamino-1-methoxy-2,3-dimethylbenzene 

Relevant articles and documents

Synthesis of 4-deoxycarbazomycin B: A convenient alternative

4-Deoxycarbazomycin B(3) was synthesized by condensation of 4-methoxy-2,3-dimethylacetanilide (8) with bromobenzene in presence of cuprous iodide and potassium carbonate, and subsequent hydrolysis with 20% aqueous ethanolic KOH, followed by cyclisation of the resulting substituted diphenylamine (9) with palladium acetate in acetic acid.

Aminocoumaran derivatives, their production and use

A novel aminocoumaran derivatives of the general formula (I): STR1 wherein R1 and R2 are a hydrogen atom, an acyl group, an alkoxycarbonyl group, an aliphatic group or aromatic group; R3 R4 and R5 are an optionally acylated hydroxyl optionally substituted amino group, alkoxy group or aliphatic group, or two of R3, R4 and R5 may be linked together to form a carbocyclic group; R6 and R7 are an aliphatic group and at least one of them has a methylene group at the α-position; R8 and R9 are a hydrogen atom or an aliphatic group or aromatic group, or a salt thereof is useful for medicines for preventing and treating various diseases such as arterial schleosis, hepatopathy, cerebrovascular diseases and the like.

Photochemical hydroxylation of 7,8-dimethylalloxazine (lumichrome). Structure elucidation of the irradiation product

The synthesis of 8-methoxy-3-(methoxycarbonyl)-6,7-dimethyl-2-(methylamino)quinoxaline is described.The synthesized compound appeared to be identical with the product obtained by degradation of the irradiation product of lumichrome.From this the conclusion is drawn that the irradiation product of lumichrome in water is 9-hydoxylumichrome.