23722-52-3

Basic information

• Product Name: Ethanone, 2-diazo-1-(3,4-dichlorophenyl)-
• CAS NO: 23722-52-3
• Molecular Formula: C8H4Cl2N2O
• Molecular Weight: 215.039
• Mol File: 23722-52-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-diazo-1-(3,4-dichlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-diazo-1-(3,4-dichlorophenyl)-(23722-52-3)
• EPA Substance Registry System: Ethanone, 2-diazo-1-(3,4-dichlorophenyl)-(23722-52-3)

Safety Data

• Hazardous Substances Data: 23722-52-3(Hazardous Substances Data)

Upstream product

• 2642-63-9 3',4'-dichloroacetophenone 
• 51-44-5 3,4-dichlorbenzoic acid 
• 186581-53-3 diazomethane 
• 3024-72-4 3,4-dichlorobenzoyl chloride 
• 162251-00-5 3-(3,4-Dichloro-phenyl)-3-oxo-propionaldehyde 

Downstream Products

• 1285704-80-4 (E)-4-ethyl 1-methyl 2-(4-methoxyphenyl)fumarate 
• 132545-38-1 (E)-4-ethyl 1-methyl 2-phenylfumarate 
• 1520-50-9 but-2-enedioic acid diethyl ester 
• 1285705-13-6 (E)-methyl 4-(3,4-dichlorophenyl)-4-oxo-2-phenylbut-2-enoate 
• 5807-30-7 3,4-dichlorophenyl acetic acid 
• 6831-55-6 2-(3,4-dichlorophenyl)acetyl chloride 

Relevant articles and documents

Rhodium(II)-catalyzed cross-coupling of diazo compounds

Nothing left to chance: A convenient protocol for selective cross-coupling of diazo compounds for the convergent synthesis of alkenes was developed (see scheme; EDG=aryl, heteroaryl, vinyl; R=O-alkyl, aryl). The selectivity control elements were identifie

40. Diazoaldehyde chemistry: Part 3. Synthesis of 4-acyl-1H-1,2,3-triazole derivatives

Ten new α -diazo-β-oxoaldehydes were condensed with aniline, ammonia, hydroxylamine, and semicarbazide to yield new 4-acyl-(1-substituted)-1H-1,2,3-triazoles in moderate-to-good yields. The method is simple and regiospecific. The latter feature makes this method superior to the widely used acylacetylene + azide approach.