85739-50-0

Basic information

• Product Name: C₁₅H₁₅N
• Synonyms: C₁₅H₁₅N
• CAS NO: 85739-50-0
• Molecular Weight: 209.291
• Mol File: 85739-50-0.mol
• Article Data: 16

Chemical Properties

• CAS DataBase Reference: C₁₅H₁₅N(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₅H₁₅N(85739-50-0)
• EPA Substance Registry System: C₁₅H₁₅N(85739-50-0)

Safety Data

• Hazardous Substances Data: 85739-50-0(Hazardous Substances Data)

Upstream product

• 1312030-02-6 chalcone-imine 
• 94-41-7 benzalacetophenone 
• 6502-38-1 chalcone oxime 
• 1024757-02-5 N-[(2E)-1,3-diphenyl-2-propen-1-yl]-4-nitrobenzenesulfonamide 
• 774-48-1 (diethoxymethyl)benzene 
• 51608-60-7 N-(benzylidene)-p-methylbenzenesulfonamide 
• 292639-13-5 (E)-N-(1,3-diphenylallyl)-4-methylbenzenesulfonamide 
• 87751-69-7 rac-(E)-1,3-diphenyl-3-acetoxy-prop-1-ene 
• 4248-19-5 tert-butyl carbazate 
• 3412-44-0 (1E)-1,3-diphenylpropene 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 52322-76-6 1,3-diphenyl-3-methoxyaminopropan-1-one 
• 7570-84-5 trans-2-phenyl-3-benzoylaziridine 
• 72923-08-1 3-imino-1,3-diphenyl-N-(4-methylphenyl)-prop-1-enylamine 

Downstream Products

• 1289143-00-5 C₂₃H₂₁NO 
• 1174154-30-3 (R,E)-N-(1,3-diphenylallyl)benzamide 
• 1289142-69-3 (S,E)-N-(1,3-diphenylallyl)benzamide 
• 1356494-19-3 (E)-1,3-diphenyl-2-propene-1-amine hydrochloride 
• 292639-13-5 (E)-N-(1,3-diphenylallyl)-4-methylbenzenesulfonamide 
• 174709-05-8 (E)-1,3-diphenyl-3-(N,N-diallylamino)propene 

Relevant articles and documents

Rh(iii)-Catalyzed allylic C-H amidation of unactivated alkenes within situgenerated iminoiodinanes

Rh(iii)-catalyzed allylic C-H amidation of substituted alkenes within situgenerated iminoiodinanes is demonstrated. The presented protocol is compatible with differently functionalized unactivated terminal alkenes and internal alkenes. In terminal alkenes

Kinetic resolution of primary allylic amines via palladium-catalyzed asymmetric allylic alkylation of malononitriles

A range of primary allylic amines were resolved with selectivity factors of up to 491 through [Pd(allyl)Cl]2/(S)-BINAP-catalyzed and mesitylsulfonyl hydrazide-accelerated asymmetric allylic alkylation of malononitriles involving enantioselectiv

Electrophilic addition of allylic carbocations to 2-cyclopropylidene-2- arylethanols: A strategy to 3-oxabicyclo[3.2.0]heptanes

We have developed an electrophilic addition of allylic carbocations to 2-cyclopropylidene-2-arylethanols constructing carbon-carbon bonds with excellent regio- and stereoselectivities. The reaction affords 3-oxabicyclo[3.2.0]heptanes in moderate to good y