324738-51-4

Basic information

• Product Name: 2′-N-benzylaminophenylacetylene
• Synonyms: 2′-N-benzylaminophenylacetylene
• CAS NO: 324738-51-4
• Molecular Weight: 207.275
• Mol File: 324738-51-4.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 2′-N-benzylaminophenylacetylene(CAS DataBase Reference)
• NIST Chemistry Reference: 2′-N-benzylaminophenylacetylene(324738-51-4)
• EPA Substance Registry System: 2′-N-benzylaminophenylacetylene(324738-51-4)

Safety Data

• Hazardous Substances Data: 324738-51-4(Hazardous Substances Data)

Upstream product

• 87587-25-5 N-benzyl-2-[2-(trimethylsilyl)acetylenyl]aniline 
• 76464-99-8 N-benzyl-2-iodoaniline 
• 615-43-0 2-iodophenylamine 
• 15111-14-5 2-iodo-N-(phenylmethylene)-benzenamine 
• 100-52-7 benzaldehyde 
• 103529-16-4 2-[(trimethylsilyl)ethynyl]aniline 
• 1066-54-2 trimethylsilylacetylene 

Downstream Products

• 324738-52-5 benzyl(2-ethynylphenyl)carbamyl chloride 
• 18217-64-6 (E)-1-benzyl-3-(methoxycarbonyl)methylene-1,3-dihydroindol-2-one 
• 1562569-64-5 4-benzyl-3-tosyl-3,4-dihydro-[1,2,3]triazolo[4,5-b]indole 
• 1615652-89-5 1-benzyl-3-diethoxyphosphoryloxy-4-methylene-3-phenyl-3,4-dihydro-2-quinolone 
• 1615653-09-2 1-benzyl-3-diisopropoxyphosphoryloxy-4-methylene-3-phenyl-3,4-dihydro-2-quinolone 
• 1615653-11-6 1-benzyl-3-diethoxyphosphoryloxy-3-(4-methoxyphenyl)-4-methylene-3,4-dihydro-2-quinolone 
• 1615653-25-2 C₂₈H₃₀NO₆P 
• 1615653-12-7 1-benzyl-3-(4-chlorophenyl)-3-diethoxyphosphoryloxy-4-methylene-3,4-dihydro-2-quinolone 
• 1615653-26-3 C₂₇H₂₇ClNO₅P 
• 1615653-13-8 1-benzyl-3-diethoxyphosphoryloxy-3-(4-fluorophenyl)-4-methylene-3,4-dihydro-2-quinolone 
• 1615653-27-4 C₂₇H₂₇FNO₅P 
• 1615653-14-9 1-benzyl-3-diethoxyphosphoryloxy-3-(3-methoxyphenyl)-4-methylene-3,4-dihydro-2-quinolone 
• 1615653-28-5 C₂₈H₃₀NO₆P 
• 1615653-15-0 1-benzyl-3-diethoxyphosphoryloxy-4-methylene-3-(2-methylphenyl)-3,4-dihydro-2-quinolone 

Relevant articles and documents

Photoinduced synthesis of fluorinated dibenz[: B, e] azepines via radical triggered cyclization

A simple, mild and efficient approach to access fluorinated dibenz[b,e]azepines via visible-light photoredox catalysis is presented. Inexpensive and commercially available fluoroalkyl anhydrides in concert with pyridine N-oxide are employed as the source

Indazole 2-oxides compound and method for preparing indazole 2-oxides compound for providing a nitrogen heterocyclic compound used as a precursor for drugs

Provided is a method for preparing an indazole 2-oxides compound, which comprises the step of: performing a cyclization reaction on 2-alkynyl aniline compound and tert-butylnitrite represented by formula (1) in the presence of bis(dibenzylideneacetone) palladium so as to produce an indazole 2-oxides compound, in which, in the formulae (1) and (2), R1 , R2 , R3 and R4 are each hydrogen, halogen or alkyl group; X1 represents an alkyl group, a first chemical structure, a second chemical structure or a third chemical structure where T1 , T2 , T3 , T4 and T5 are each hydrogen, halogen, alkoxy group, or alkyl group; X2 represents hydrogen, cycloalkyl group, alkyl group, alkenyl group, thienyl group, unsubstituted phenyl group, or substituted phenyl group, where the substituent is selected from the group consisting of an alkyl group, an alkoxy group, a halogen, a haloalkyl group, -CN, or -NO2.

Bis(dibenzylideneacetone)palladium(0)/tert-Butyl Nitrite- Catalyzed Cyclization of o-Alkynylanilines with tert-Butyl Nitrite: Synthesis and Applications of Indazole 2-Oxides

An efficient method for the synthesis of 1-benzyl/arylindazole 2-oxides via a bis(dibenzylideneacetone)palladium(0) [Pd(dba)2]/tert-butyl nitrite (TBN)-catalyzed reaction of o-alkynylaniline derivatives with TBN is reported. The overall transfo