86412-57-9

Basic information

• Product Name: N-(4-Chloro-2-Methoxyphenyl)acetaMide
• Synonyms: N-(4-Chloro-2-Methoxyphenyl)acetaMide
• CAS NO: 86412-57-9
• Molecular Formula: C₉H₁₀ClNO₂
• Molecular Weight: 199.6342
• Product Categories: Amines, Aromatics, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 86412-57-9.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(4-Chloro-2-Methoxyphenyl)acetaMide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-Chloro-2-Methoxyphenyl)acetaMide(86412-57-9)
• EPA Substance Registry System: N-(4-Chloro-2-Methoxyphenyl)acetaMide(86412-57-9)

Safety Data

• Hazardous Substances Data: 86412-57-9(Hazardous Substances Data)

Usage

Uses

N-(4-Chloro-2-methoxyphenyl)acetamide (cas# 86412-57-9) is a compound useful in organic synthesis.

Upstream product

• 5877-56-5 N-benzylidene-2-methoxy-aniline 
• 75-36-5 acetyl chloride 
• 13726-14-2 4-chloro-m-anisidine 
• 67-56-1 methanol 
• 539-03-7 N-(4-chlorophenyl)acetamide 
• 91-23-6 2-Nitroanisole 
• 135055-92-4 Ethyl 4-chloro-2-methoxycarbanilate 
• 57479-70-6 2-methoxy-4-chlorobenzoic acid 
• 16323-09-4 N-(4-chloro-2-hydroxyphenyl)acetamide 
• 77-78-1 dimethyl sulfate 
• 93-50-5 4-chloro-o-anisidine 
• 108-24-7 acetic anhydride 
• 93-26-5 2-methoxyacetanilide 
• 112160-74-4 acetic acid-(2,4,N-trichloro-anilide) 

Downstream Products

• 103153-92-0 bis-(4-acetylamino-5-methoxy-2-nitro-phenyl)-disulfide 
• 135055-93-5 4'-Chloro-N-phenyl-o-acetanisidide 

Relevant articles and documents

HETEROCYCLIC COMPOUNDS AS MUTANT IDH INHIBITORS

The present disclosure relates generally to compounds useful in treatment of conditions associated with mutant isocitrate dehydrogenase (mt-IDH), particularly mutant IDH1 enzymes. Specifically, the present invention discloses compound of formula (IA), which exhibits inhibitory activity against mutant IDH1 enzymes. Method of treating conditions associated with excessive activity of mutant IDH1 enzymes with such compound is disclosed. Uses thereof, pharmaceutical composition, and kits are also disclosed.

Reexamination of the Thermolytic Rearrangement of 4-Halophenyl Azides to 2-Aminophenols and other Products

The halogenation of derivatives of 2-aminophenol with N-chloro- and N-bromosuccinimides at ambient temperatures in acetic acid was studied.With the necessary compounds available, a reexamination of the thermolytic rearrangement of 2-halophenyl azides to 2-aminophenols and other products was undertaken.It is certain that the rearrangement of 4-halophenyl azides to 2-aminophenols occurs but the products identified in this study differ significantly from those reported previously by Suschitzky et al. (1963, 1966). Keywords: Acetylated-2-amino-5-halophenols; 2-Acetamido-5-haloanisoles; 6-Halo-2-methylbenzoxazoles; 6-Halobenzoxazolones; 6-Halotriacetylaminophenols; 1H-NMR spectra; Fungicidal activity.