39520-63-3

Basic information

• Product Name: 2-Penten-1-ol, 5-phenyl-
• CAS NO: 39520-63-3
• Molecular Formula: C11H14O
• Molecular Weight: 162.232
• Mol File: 39520-63-3.mol
• Article Data: 27

Chemical Properties

• CAS DataBase Reference: 2-Penten-1-ol, 5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Penten-1-ol, 5-phenyl-(39520-63-3)
• EPA Substance Registry System: 2-Penten-1-ol, 5-phenyl-(39520-63-3)

Safety Data

• Hazardous Substances Data: 39520-63-3(Hazardous Substances Data)

Upstream product

• 16900-77-9 5-phenyl-2-pentynol 
• 104-53-0 3-phenyl-propionaldehyde 
• 50-00-0 formaldehyd 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 930-22-3 epoxybutene 
• 2549-99-7 benzyl triethoxysilane 
• 26429-96-9 (Z)-5-phenyl-2-pentenoic acid methyl ester 
• 88842-13-1 (Z-)-ethyl 5-phenylpent-2-enoate 
• 129042-95-1 methyl 5-phenylpent-2-enoate 
• 93888-06-3 1-(oxiran-2-yl)-3-phenylpropan-1-ol 
• 37904-38-4 5-phenylpent-1-en-3-ol 
• 74940-41-3 1-(tributylstannyl)-5-phenyl-2-pentene 
• 6790-38-1 1,2-epoxy-3-vinylpropane 
• 100-56-1 phenylmercury(II) chloride 

Downstream Products

• 1318801-84-1 (Z)-3-iodo-5-phenylpent-2-en-1-ol 
• 1318801-85-2 (Z)-3-iodo-5-phenylpent-2-enal 
• 1318801-75-0 C₁₅H₁₆O₂ 
• 1318801-86-3 C₁₂H₁₃I 
• 1318801-69-2 (Z)-4-phenethylhepta-4,6-diene-2,3-dione 
• 1318801-74-9 C₁₅H₁₆O₂ 
• 945428-61-5 (E)-1-benzyloxy-5-phenylpent-2-ene 
• 945428-60-4 (Z)-1-benzyloxy-5-phenylpent-2-ene 
• 75553-23-0 (E)-5-phenyl-2-penten-1-ol 
• 1075-74-7 5-phenylpent-1-ene 

Relevant articles and documents

Stereoselective Carbocyclization of Vinyloxiranes Catalyzed by Lewis Acids: Construction of the Musellarin Tricyclic Core

Stereoselective carbocyclizations of vinyloxiranes were efficiently catalyzed by Lewis acids to provide cyclic homoallyl alcohols as single isomers. The choice of Lewis acid, B(C6F5)3 was crucial for the stereoselective tr

Cascade reaction including a formal [5?+?2] cycloaddition by use of alkyne-Co2(CO)6 complex

A new cascade reaction including formal [5 + 2] cycloaddition was developed. Treatment of homocinnamyl alcohol and Co2(CO)6-complexed arylpropynal with BF3·OEt2 resulted in the generation of hydrobenzocyclohepta

Tandem Catalysis: Transforming Alcohols to Alkenes by Oxidative Dehydroxymethylation

We report a Rh-catalyst for accessing olefins from primary alcohols by a C-C bond cleavage that results in dehomologation. This functional group interconversion proceeds by an oxidation-dehydroformylation enabled by N,N-dimethylacrylamide as a sacrificial acceptor of hydrogen gas. Alcohols with diverse functionality and structure undergo oxidative dehydroxymethylation to access the corresponding olefins. Our catalyst protocol enables a two-step semisynthesis of (+)-yohimbenone and dehomologation of feedstock olefins.