35281-62-0

Basic information

• Product Name: Benzenemethanol, a-(1-ethenylidenepentyl)-
• CAS NO: 35281-62-0
• Molecular Formula: C14H18O
• Molecular Weight: 202.296
• Mol File: 35281-62-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, a-(1-ethenylidenepentyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, a-(1-ethenylidenepentyl)-(35281-62-0)
• EPA Substance Registry System: Benzenemethanol, a-(1-ethenylidenepentyl)-(35281-62-0)

Safety Data

• Hazardous Substances Data: 35281-62-0(Hazardous Substances Data)

Upstream product

• 18495-26-6 1-bromo-2-heptyne 
• 100-52-7 benzaldehyde 
• 109-72-8 n-butyllithium 
• 16156-58-4 prop-2-yn-1-ol methanesulfonate 
• 693-03-8 n-butyl magnesium bromide 
• 13280-09-6 4-chloro-1-phenyl-2-butyn-1-ol 
• 32904-84-0 4-hydroxy-4-phenyl-2-butynyl methyl ether 
• 693-04-9 butyl magnesium bromide 
• 100859-51-6 1-chloro-2-heptyne 

Downstream Products

• 1422370-66-8 4-butyl-3-pentyl-5-phenyl-2(5H)-furanone 
• 3437-90-9 3-benzylideneheptan-2-one 
• 1344703-78-1 2-(n-butyl)-5,5,6,6,7,7,8,8,8-nonafluoro-3-iodo-1-phenyl-2-octen-1-ol 
• 1276669-04-5 methyl 2-butyl-1-phenyl-2,3-butadien-1-yl carbonate 
• 1276669-16-9 (E)-3-butyl-4-phenyl-1,3-butadien-2-yl 4-nitrobenzoate 
• 1276669-03-4 2-butyl-1-phenyl-2,3-butadien-1-yl 4-nitrobenzonate 
• 1276668-98-4 2-butyl-1-phenyl-2,3-butadien-1-yl acetate 
• 123707-41-5 (E)-3-butyl-4-phenyl-3-buten-2-one 
• 1276669-17-0 (E)-methyl 3-butyl-4-phenyl-1,3-butadien-2-yl carbonate 
• 1276668-88-2 (E)-3-butyl-1-iodo-4-phenyl-3-buten-2-one 
• 1276669-21-6 (Z)-3-butyl-4-phenyl-1,3-butadien-2-yl acetate 
• 1276669-11-4 (E)-3-butyl-4-phenyl-1,3-butadien-2-yl acetate 
• 1039769-77-1 3-butyl-2-phenyl-4-(5'-phenyl-1',3'-pentadien-3'(E)-2'-yl)-2,5-dihydrofuran 
• 1039769-37-3 3-butyl-2-phenyl-4-(1',3'-butadien-2'-yl)-2,5-dihydrofuran 

Relevant articles and documents

Copper-Catalyzed Direct and Stereoselective Synthesis of Conjugated Enynes from α-Allenols

A novel strategy for the stereoselective synthesis of conjugated enynes directly from α-allenols has been developed. The reaction proceeds with perfect E-selectivity and exhibits high functional group compatibility. This catalytic system can also be applied to the stereoselective synthesis of conjugated dienynes and enediynes. (Figure presented.).

An efficient CuCN-catalyzed synthesis of optically active 2,3-allenols from optically active 1-substituted 4-chloro-2-butyn-1-ols

(Chemical Equation Presented) The sequential treatment of optically active terminal propargylic alcohols with n-BuLi/(HCHO)n and regioselective chlorination afforded the corresponding optically active 4-chloro-2-butyn-1-ols. With R1

PdI2-catalyzed coupling-cyclization reactions involving two different 2,3-allenols: An efficient synthesis of 4-(1′,3′-dien- 2′-yl)-2,5-dihydrofuran derivatives

Transition-metal-catalyzed dimeric coupling-cyclization reactions of two different 2,3-allenols afforded 4-(1′,3′-dien-2′-yl)-2,5- dihydrofuran derivatives 3. 2-Substituted 2,3-allenols 1 cyclized to form the 2,5-dihydrofuran ring, whereas the 2-unsubstit