75553-23-0

Basic information

• Product Name: 2-Penten-1-ol, 5-phenyl-, (2E)-
• CAS NO: 75553-23-0
• Molecular Formula: C11H14O
• Molecular Weight: 162.232
• Mol File: 75553-23-0.mol
• Article Data: 70

Chemical Properties

• CAS DataBase Reference: 2-Penten-1-ol, 5-phenyl-, (2E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Penten-1-ol, 5-phenyl-, (2E)-(75553-23-0)
• EPA Substance Registry System: 2-Penten-1-ol, 5-phenyl-, (2E)-(75553-23-0)

Safety Data

• Hazardous Substances Data: 75553-23-0(Hazardous Substances Data)

Upstream product

• 26429-97-0 methyl (2E)-5-phenyl-2-pentenoate 
• 126435-89-0 (E)-5-phenyl-2-penten-1-ol acetate 
• 39520-63-3 (Z)-5-phenylpent-2-en-1-ol 
• 16520-62-0 4-Phenyl-1-butyne 
• 104-53-0 3-phenyl-propionaldehyde 
• 930-22-3 epoxybutene 
• 2549-99-7 benzyl triethoxysilane 
• 1236009-38-3 [(2R,3R)-3-(2-phenylethyl)thiiran-2-yl]methyl dimethylcarbamate 
• 24271-22-5 5-phenyl-2(E)-pentenoic acid 
• 55282-95-6 ethyl (2E)-5-phenylpent-2-enoate 
• 485809-19-6 5-phenyl-2-pentenoic acid chloride 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 6790-38-1 1,2-epoxy-3-vinylpropane 
• 100-56-1 phenylmercury(II) chloride 

Downstream Products

• 142096-79-5 (-)-(1R,2R)-2-(2-phenylethyl)cyclopropylmethanol 
• 142096-79-5 (+)-(1S,2S)-2-(2-phenylethyl)cyclopropylmethanol 
• 125303-61-9 [(2S,3S)-3-phenethyloxiran-2-yl]methanol 
• 154428-47-4 (2R,3R)-trans-2,3-epoxy-5-phenyl-1-pentanol 
• 138662-21-2 (2S,3R)-2,3-epoxy-5-phenylpentan-1-ol 
• 100564-78-1 (2R)-(tert-butoxycarbonylamino)-4-phenylbutanoic acid 
• 82732-07-8 Boc-L-homophenylalanine 
• 154079-57-9 (2S,3S)-3-(tert-butoxycarbonylamino)-5-phenyl-1,2-pentanediol 
• 154079-56-8 (2S,3S)-3-diphenylmethylamino-5-phenyl-1,2-pentanediol 
• 74940-33-3 Dithiocarbonic acid S-methyl ester S-(1-phenethyl-allyl) ester 
• 71292-39-2 Ethyl 3-(2-phenylethyl)-4-pentenoate 
• 126435-89-0 (E)-5-phenyl-2-penten-1-ol acetate 
• 639005-99-5 (E)-(5-chloropent-3-en-1-yl)benzene 
• 639004-50-5 (Z)-(5-chloro-3-penten-1-yl)benzene 

Relevant articles and documents

Ligand-controlled cobalt-catalyzed remote hydroboration and alkene isomerization of allylic siloxanes

The Co-catalyzed remote hydroboration and alkene isomerization of allylic siloxanes were realized by a ligand-controlled strategy. The remote hydroboration with dcype provided borylethers, while xantphos favored the formation of silyl enol ethers.

Iridium-Catalyzed Regioselective Hydroalkynylation of Internal Alkenes Directed by an Oxime

We report here an iridium-catalyzed hydroalkynylation of allylic alcohols protected by an oxime group. Catalytic alkynylation occurs exclusively at the distal position of the alkene. This method generates γ-alkynyl alcohol oximes directly from internal alkenes and terminal alkynes. The oxime group can be readily removed to afford a free alcohol, thus providing an indirect route for the catalytic hydroalkynylation of allylic alcohols.

Copper-Catalyzed Perfluoroalkylation of Allyl Phosphates with Stable Perfluoroalkylzinc Reagents

A general and practical method for copper-catalyzed cross-coupling of allyl phosphates with stable perfluoroalkylzinc reagents has been developed. The reaction proceeds under mild reaction conditions with high efficiency, good functional group tolerance, and high regio- A nd stereoselectivities and provides general, straightforward, and useful access to allyl-perfluoroalkyl compounds. Preliminary mechanistic studies reveal that the allyl copper intermediate may be involved in the catalytic cycle.