51223-59-7

Basic information

• Product Name: N-(2-amino-4-chlorophenyl)acetamide(SALTDATA: FREE)
• Synonyms: N-(2-amino-4-chlorophenyl)acetamide(SALTDATA: FREE)
• CAS NO: 51223-59-7
• Molecular Formula: C₈H₉ClN₂O
• Molecular Weight: 184.62286
• Mol File: 51223-59-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 393.734°C at 760 mmHg
• Flash Point: 191.923°C
• Appearance: /
• Density: 1.35g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.646
• CAS DataBase Reference: N-(2-amino-4-chlorophenyl)acetamide(SALTDATA: FREE)(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-amino-4-chlorophenyl)acetamide(SALTDATA: FREE)(51223-59-7)
• EPA Substance Registry System: N-(2-amino-4-chlorophenyl)acetamide(SALTDATA: FREE)(51223-59-7)

Safety Data

• Hazardous Substances Data: 51223-59-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C8H9ClN2O/c1-5(12)11-8-3-2-6(9)4-7(8)10/h2-4H,10H2,1H3,(H,11,12)

Upstream product

• 881-51-6 N-(4-chloro-2-nitrophenyl)-acetamide 
• 539-03-7 N-(4-chlorophenyl)acetamide 

Downstream Products

• 21639-42-9 acetic acid-(4-chloro-2-phenylazo-anilide) 
• 84445-86-3 1-(5-Chloro-2-mercapto-benzoimidazol-1-yl)-ethanone 
• 25369-78-2 5-chloro-1H-benzoimidazole-2-thiol 
• 86569-38-2 N-acetyl-N'-butyryl-4-chloro-1,2-phenylenediamine 
• 113001-04-0 N-(4-Chloro-2-{[1-(5-chloro-2-nitro-phenyl)-meth-(Z)-ylidene]-amino}-phenyl)-acetamide 
• 2818-69-1 5-chloro-2-methyl-1H-benzimidazole 
• 86569-36-0 N,N'-diacetyl 4-chloro-1,2-phenylenediamine 
• 86569-37-1 N-acetyl-N'-propionyl-4-chloro-1,2-phenylenediamine 
• 113001-02-8 N-(4-Chloro-2-{[1-(2-nitro-phenyl)-meth-(Z)-ylidene]-amino}-phenyl)-acetamide 
• 113001-15-3 2-amino-6-chloro-3-(5-chloro-2-nitrophenyl)quinoxaline 
• 21639-43-0 4-chloro-2-phenylazo-aniline 

Relevant articles and documents

Fe-Catalyzed Amination of (Hetero)Arenes with a Redox-Active Aminating Reagent under Mild Conditions

A novel and efficient Fe-catalyzed direct C?H amination (NH2) of arenes is reported using a new redox-active aminating reagent. The reaction is simple, and can be performed under air, mild, and redox-neutral conditions. This protocol has a broad substrate scope and could be used in the late-stage modification of bioactive compounds. Mechanistic studies demonstrate that a radical pathway could be involved in this transformation.

SYNTHESIS AND PESTICIDAL ACTIVITY OF N,N'-DIACYL DERIVATIVES OF 4-CHLORO-1,2-PHENYLENDIAMINE

The acylation of 2-aminoacyl-chloroanilines with acid anhydrides has given N,N'-diacyl derivatives of 4-chloro-1,2-phenylenediamine.Their fungicidal activities have been investigated.It has been shown that in cotton plants they are converted into 2-alkyl-5-chlorobenzimidazoles.