52686-70-1

Basic information

• Product Name: Benzene, (1-diazopropyl)-
• CAS NO: 52686-70-1
• Molecular Formula: C9H10N2
• Molecular Weight: 146.192
• Mol File: 52686-70-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzene, (1-diazopropyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (1-diazopropyl)-(52686-70-1)
• EPA Substance Registry System: Benzene, (1-diazopropyl)-(52686-70-1)

Safety Data

• Hazardous Substances Data: 52686-70-1(Hazardous Substances Data)

Upstream product

• 36590-52-0 N-phenyl-p-chlorobenzohydrazonoyl chloride 
• 93-55-0 1-phenyl-propan-1-one 
• 32770-66-4 1-(1-phenylpropylidene)hydrazine 
• 17336-66-2 propiophenone N-tosylhydrazone 

Downstream Products

• 130690-81-2 (3R,4R)-4-Chloro-3-ethyl-3-phenyl-5,5-bis-trimethylsilanyl-4,5-dihydro-3H-[1,2,4]diazaphosphole 
• 130690-81-2 (3S,4R)-4-Chloro-3-ethyl-3-phenyl-5,5-bis-trimethylsilanyl-4,5-dihydro-3H-[1,2,4]diazaphosphole 
• 873-66-5 1-propenylbenzene 
• 766-90-5 cis-1-phenyl-1-propylene 
• 824-90-8 1-phenylbut-1-ene 
• 93-54-9 1-Phenyl-1-propanol 
• 72379-99-8 bis-(1-phenyl-propylidene)-hydrazine 
• 20306-86-9 N-(1-phenylpropyl)acetamide 
• 61574-05-8 C₉H₁₀ 
• 93-89-0 benzoic acid ethyl ester 
• 93-55-0 1-phenyl-propan-1-one 
• 637-50-3 1-phenylpropene 
• 108-95-2 phenol 
• 175274-19-8 (S)-1,2-diphenylbutan-1-one 

Relevant articles and documents

alpha-aryl or alkyl substituted borane adduct, preparation method and applications thereof

The invention relates to an alpha-aryl or alkyl substituted borane adduct, a preparation method and applications thereof, specifically to preparation of an alpha-aryl or alkyl substituted borane adduct by carrying out a reaction on hydrazone as an unstabl

A Novel Synthesis of Arylsulfonyl Hydrazine Derivatives Via the Reaction of Arylsulfonyl Hydrazone Salts and Hydrazonoyl Chlorides

An efficient method for the synthesis of arylsulfonyl hydrazines and diazo compounds via arylsulfonyl hydrazone salts is described. The reaction was performed in DMF using hydrazonoyl chlorides and sodium arylsulfonyl hydrazones, which were easily prepare

The β-heteroatom effect on carbenes

The β-thiophosphinoyl carbene PhCCH2P(S)Ph2 (5) has been prepared by irradiation of the corresponding diazo compound. The relative rates for insertion into the OH bond of methanol and for addition to the double bond of 2-methyl-2-but