6947-29-1

Basic information

• Product Name: Acetic acid,2-(4-chlorophenyl)hydrazide
• Synonyms: Aceticacid, 2-(p-chlorophenyl)hydrazide (8CI); 1-(4-Chlorophenyl)-2-acetylhydrazine;NSC 56916; N'-(4-Chlorophenyl)acetohydrazide
• CAS NO: 6947-29-1
• Molecular Formula: C8H9 Cl N2 O
• Molecular Weight: 184.625
• Mol File: 6947-29-1.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 247.6°Cat760mmHg
• Flash Point: 103.5°C
• Density: 1.288g/cm³
• CAS DataBase Reference: Acetic acid,2-(4-chlorophenyl)hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid,2-(4-chlorophenyl)hydrazide(6947-29-1)
• EPA Substance Registry System: Acetic acid,2-(4-chlorophenyl)hydrazide(6947-29-1)

Safety Data

• Hazardous Substances Data: 6947-29-1(Hazardous Substances Data)

Upstream product

• 106-47-8 4-chloro-aniline 
• 64-19-7 acetic acid 
• 1073-69-4 N-4-chlorophenylhydrazine 
• 108-24-7 acetic anhydride 
• 100-63-0 phenylhydrazine 
• 17333-85-6 4-chlorophenyldiazonium salt 
• 579-07-7 1-Phenylpropane-1,2-dione 
• 70638-34-5 2-(4-chloro-phenylazo)-2,5-dimethyl-furan-3-one 
• 1073-70-7 4-chlorophenylhydrazine hydrochloride 

Downstream Products

• 1312713-62-4 1-(8-(4-chlorophenyl)-3-(2-fluorophenyl)-1-oxa-2,7,8-triazaspiro[4.4]non-2-en-7-yl)ethanone 
• 1450812-51-7 N'-(4-chlorophenyl)-N'-methylacetohydrazide 
• 39195-66-9 2-(4-chlorophenyl)benzofuran 
• 906781-10-0 2-(4-chlorophenyl)-1H-benzo[g]indole 
• 1657-50-7 (E)-1-(4-chlorophenyl)-2-phenylethene 
• 92126-19-7 dimethyl 1-(4-chlorophenyl)-5-methyl-1H-pyrazole-3,4-dicarboxylate 
• 52598-02-4 2,3-diphenyl-5-chloro-1H-indole 
• 681860-24-2 N,N'-dimethyl-N'-(4-chlorophenyl)acetohydrazide 
• 1073-69-4 N-4-chlorophenylhydrazine 
• 804-88-6 4-(4-chloro-phenyl)-2-methyl-6,6-diphenyl-4H-[1,3,4]oxadiazin-5-one 

Relevant articles and documents

Palladium/copper-catalyzed arylation of alkenes with N′-acyl arylhydrazines

A novel ligand-free palladium/copper-catalyzed Heck-type coupling reaction of alkenes and N′-acyl arylhydrazines has been developed by using air as the terminal oxidant. This protocol features wide functional group tolerance and produces highly chemoselective and regioselective products with good to excellent yields.

Rh(III)-catalyzed oxidative coupling of 1,2-disubstituted arylhydrazines and olefins: A new strategy for 2,3-dihydro-1H-indazoles

A rhodium(III)-catalyzed oxidative olefination of 1,2-disubstituted arylhydrazines with alkenes via sp2 C-H bond activation followed by an intramolecular aza-Michael reaction is described. This strategy allows the direct and efficient construct

Formation of enehydrazine intermediates through coupling of phenylhydrazines with vinyl halides: Entry into the Fischer indole synthesis

Cut to the chase: Direct formation of an enehydrazine, an intermediate in the classic Fischer indole synthesis, solves the regioselectivity problem associated with indolization. This approach not only achieves selective synthesis of indoles through proper selection of the vinyl halide, but also leads to quick construction of desoxyeseroline and esermethole, as well as the key structural motif in the Akuammiline alkaloid vincorine. Copyright