81176-43-4

Basic information

• Product Name: (S,E)-4-Phenyl-3-butene-2-ol
• Synonyms: (2S,3E)-4-Phenyl-3-butene-2-ol;(S)-1-[(E)-Styryl]ethanol;(S,E)-4-Phenyl-3-butene-2-ol;[2S,3E,(-)]-4-Phenyl-3-buten-2-ol;[S,E,(-)]-4-Phenyl-3-buten-2-ol
• CAS NO: 81176-43-4
• Molecular Formula: C₁₀H₁₂O
• Molecular Weight: 0
• Mol File: 81176-43-4.mol
• Article Data: 187

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (S,E)-4-Phenyl-3-butene-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (S,E)-4-Phenyl-3-butene-2-ol(81176-43-4)
• EPA Substance Registry System: (S,E)-4-Phenyl-3-butene-2-ol(81176-43-4)

Safety Data

• Hazardous Substances Data: 81176-43-4(Hazardous Substances Data)

Usage

General Description

(S,E)-4-Phenyl-3-butene-2-ol is a chemical compound with the molecular formula C10H14O. It is an unsaturated alcohol that consists of a butene backbone with a phenyl group attached to one of the carbon atoms. (S,E)-4-Phenyl-3-butene-2-ol is often used in the synthesis of various organic compounds and is also known for its pleasant floral aroma. It can be found in a variety of natural sources, including certain flowers and plants. Additionally, (S,E)-4-Phenyl-3-butene-2-ol is utilized in the production of fragrances, flavors, and other aromatic products due to its unique olfactory properties. Overall, this compound has several important industrial and commercial applications, making it a valuable chemical in the field of organic chemistry.

Upstream product

• 87246-95-5 (R)-(-)-α-Phenyl-γ-methylallyl alcohol 
• 36004-04-3 ethyl (E)-1-phenylbut-1-en-3-ol 
• 14371-10-9 (E)-3-phenylpropenal 
• 544-97-8 dimethyl zinc(II) 
• 134837-48-2 (S)-1-{[Dimethyl-((E)-(S)-1-methyl-3-phenyl-allyl)-silanyl]-methyl}-2-methoxymethyl-pyrrolidine 
• 95482-80-7 1-(4-methylphenylsulfinyl)-4-phenyl-(2R,3E)-3-buten-2-ol 
• 135758-87-1 (1S,2E)-benzoic acid 1-methyl-3-phenylallyl ester 
• 1896-62-4 (E)-benzalacetone 
• 105-45-3 acetoacetic acid methyl ester 
• 108-05-4 vinyl acetate 
• 82045-04-3 (rac)-(E)-2-acetoxy-4-phenylbut-3-ene 
• 74457-38-8 (E)‐4‐phenylbut‐3‐en‐2‐yl acetate 
• 97-72-3 2-Methylpropionic anhydride 
• 123-62-6 propionic acid anhydride 

Downstream Products

• 2344-70-9 1-phenyl-3-butanol 
• 79594-10-8 (E)-(3-methylhept-1-en-1-yl)benzene 
• 96391-85-4 4-phenyl-2-octene 
• 96391-86-5 [(R)-((Z)-1-Propenyl)-pentyl]-benzene 
• 95190-90-2 (2S)-(4-phenylbut-3-en-2-yl) N-phenylbenzimidate 
• 231305-22-9 ethyl (2S,3E)-(4-phenyl-3-buten-2-yl)carbonate 
• 586341-97-1 (3R,4E)-2-methyl-3-phenylhex-4-enoic acid 
• 1174006-11-1 (S,E)-4-phenylbut-3-en-2-yl 2-(tert-butoxycarbonylamino)acetate 
• 1174006-12-2 (S)-[(S,E)-4-phenylbut-3-en-2-yl] 2-(tert-butoxycarbonylamino)propanoate 
• 1461649-10-4 (R,E)-1-methyl-4-(4-phenylbut-3-en-2-yl)benzene 

Relevant articles and documents

Chirality transfer during the [2,3]-sila-Wittig rearrangement and cyclopropanation reaction of optically active [(sec-allyloxy)silyl]lithiums

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Nickel-Catalyzed Enantioselective Hydroboration of Vinylarenes

The enantioselective hydroboration of vinylarenes catalyzed by a chiral, nonracemic nickel catalyst is presented as a facile method for generating chiral benzylic boronate esters. Various vinylarenes react with bis(pinacolato)diboron (B2pin2) in the presence of MeOH as a hydride source to form chiral boronate esters in up to 92% yield with up to 94% ee. The use of anhydrous Me4NF to activate B2pin2 is crucial for ensuring fast transmetalation to achieve high enantioselectivities.

Cobalt-Catalyzed Enantiospecific Dynamic Kinetic Cross-Electrophile Vinylation of Allylic Alcohols with Vinyl Triflates

Asymmetric cross-electrophile coupling has emerged as a promising tool for producing chiral molecules; however, the potential of this chemistry with metals other than nickel remains unknown. Herein, we report a cobalt-catalyzed enantiospecific vinylation