70078-14-7

Basic information

• Product Name: 1-(1-diazoethyl)-4-methoxybenzene
• Synonyms: 1-(1-diazoethyl)-4-methoxybenzene
• CAS NO: 70078-14-7
• Molecular Weight: 162.191
• Mol File: 70078-14-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-(1-diazoethyl)-4-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1-diazoethyl)-4-methoxybenzene(70078-14-7)
• EPA Substance Registry System: 1-(1-diazoethyl)-4-methoxybenzene(70078-14-7)

Safety Data

• Hazardous Substances Data: 70078-14-7(Hazardous Substances Data)

Upstream product

• 6310-14-1 4'-methoxyacetophenone hydrazone 
• 32117-52-5 1-(1-(4-methoxyphenyl)ethylidene)-2-tosylhydrazine 
• 100-06-1 1-(4-methoxyphenyl)ethanone 

Downstream Products

• 25287-28-9 N-phenyl[1-(4-methoxyphenyl)ethylidene]amine 
• 29338-71-4 1-bromo-1-(4-methoxyphenyl)ethene 
• 21399-34-8 1,2-bis(1-(4-methoxyphenyl)ethylidene)hydrazine 
• 637-69-4 4-Methoxystyrene 
• 130690-85-6 (3R,4R)-4-Chloro-3-(4-methoxy-phenyl)-3-methyl-5,5-bis-trimethylsilanyl-4,5-dihydro-3H-[1,2,4]diazaphosphole 
• 130690-85-6 (3S,4R)-4-Chloro-3-(4-methoxy-phenyl)-3-methyl-5,5-bis-trimethylsilanyl-4,5-dihydro-3H-[1,2,4]diazaphosphole 
• 68408-52-6 ω-Jod-4-methoxyacetophenonazin 

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

Enantioselective Synthesis of Trisubstituted Allenes via Cu(I)-Catalyzed Coupling of Diazoalkanes with Terminal Alkynes

A highly enantioselective synthesis of trisubstituted allenes has been achieved through Cu(I)-catalyzed cross-coupling of aryldiazoalkanes and terminal alkynes with chiral bisoxazoline ligands. Alkynyl migratory insertion of Cu(I) carbene is proposed as t

CYCLOADDITIONS OF DISUBSTITUTED DIAZO COMPOUNDS TO P-CHLORO(BISTRIMETHYLSILYL) METHYLENE PHOSPHINE.

Disubstituted diazo compounds rapidly add to P-chloro (bistrimethylsilyl) methylene phosphine at low temperature. 1H, 31P and 13C NMR allow the characterization of the resulting cycloadducts and the establisment of the stereochemistry of the resulting cycloadducts which are potential precursors of ?3λ5 bis methylene phosphorane by nitrogen extrusion.