554447-15-3

Basic information

• Product Name: (S)-benzoic acid N'-[1-(4-methoxyphenyl)but-3-enyl]hydrazide
• Synonyms: (S)-benzoic acid N'-[1-(4-methoxyphenyl)but-3-enyl]hydrazide
• CAS NO: 554447-15-3
• Molecular Weight: 296.369
• Mol File: 554447-15-3.mol

Chemical Properties

• CAS DataBase Reference: (S)-benzoic acid N'-[1-(4-methoxyphenyl)but-3-enyl]hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-benzoic acid N'-[1-(4-methoxyphenyl)but-3-enyl]hydrazide(554447-15-3)
• EPA Substance Registry System: (S)-benzoic acid N'-[1-(4-methoxyphenyl)but-3-enyl]hydrazide(554447-15-3)

Safety Data

• Hazardous Substances Data: 554447-15-3(Hazardous Substances Data)

Upstream product

• 14850-87-4 (E)-N′-(4-methoxybenzylidene)benzohydrazide 
• 106-95-6 allyl bromide 
• 14850-86-3 N'-(4-methoxybenzylidene)benzohydrazide 
• 107-37-9 allyltrichlorosilane 

Downstream Products

• 188425-29-8 (1S)-1-(4-methoxyphenyl)but-3-en-1-amine 

Relevant articles and documents

Indium-mediated catalytic enantioselective allylation of N -benzoylhydrazones using a protonated chiral amine

A catalytic enantioselective indium-mediated allylation of N-benzoylhydrazones in conjunction with a protonated chiral amine affording enantioenriched homoallylic amines with an extremely high level of enantioselectivity and chemical yield was developed.

The sulfinyl moiety in Lewis base-promoted allylations

By employing Senanayake's oxathiazolidine-2-oxide reagent, a collection of sulfinamides was prepared and provided the first examples of sulfinamides promoting the allylation of benzaldehyde and N-benzoylhydrazones with allyltrichlorosilane. The optimum su

Indium-mediated asymmetric allylation of acylhydrazones using a chiral urea catalyst

(Chemical Equation Presented) Urea-ka! A new role for urea-based chiral catalysts has been uncovered in the asymmetric allylation of acylhydrazones with allylindium reagents (see scheme; Bz: benzoyl). The best results were obtained using the bifunctional