129571-71-7

Basic information

• Product Name: (E)-1-phenyl-1,4-pentadien-3-ol
• CAS NO: 129571-71-7
• Molecular Weight: 160.216
• Mol File: 129571-71-7.mol
• Article Data: 31

Chemical Properties

• CAS DataBase Reference: (E)-1-phenyl-1,4-pentadien-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-phenyl-1,4-pentadien-3-ol(129571-71-7)
• EPA Substance Registry System: (E)-1-phenyl-1,4-pentadien-3-ol(129571-71-7)

Safety Data

• Hazardous Substances Data: 129571-71-7(Hazardous Substances Data)

Upstream product

• 14371-10-9 (E)-3-phenylpropenal 
• 2768-02-7 (vinyl)trimethoxylsilane 
• 593-60-2 Vinyl bromide 
• 14604-31-0 (E)-1-phenylpent-1-en-4-yn-3-ol 
• 108-86-1 bromobenzene 
• 922-65-6 divinylcarbinol 
• 1826-67-1 vinyl magnesium bromide 
• 104-55-2 3-phenyl-propenal 

Downstream Products

• 3152-68-9 (1E)-1-phenylpent-1-en-3-one 
• 1215019-99-0 C₁₉H₁₉NO₄S 
• 1434336-46-5 7-phenylspiro[5.5]undecane-1,5,9-trione 
• 1628340-90-8 (E)-4-bromo-1-phenylpent-1-en-3-one 
• 109529-98-8 ((1E,3E)-5-bromopenta-1,3-dien-1-yl)benzene 
• 58927-91-6 cis-5-phenyl-3-penten-1-ol 
• 687638-55-7 [(E)-1-phenylpenta-1,4-dien-3-yloxy](tert-butyl)dimethylsilane 
• 615547-08-5 2-((E)-Hexa-3,5-dienyl)-2-((2E,4E)-5-phenyl-penta-2,4-dienyl)-malonic acid bis-(2,2,2-trifluoro-ethyl) ester 
• 192886-57-0 (4E)-5-phenylpenta-2,4-dien-1-ol 
• 129646-80-6 (S,E)‐1‐phenylpenta‐1,4‐dien‐3‐ol 
• 135663-94-4 (1S,2S,3S)-1,2-epoxy-1-phenyl-4-penten-3-ol 
• 135663-95-5 (2R,3R)-1,2-epoxy-5-phenyl-4-penten-3-ol 
• 1004960-59-1 (R,E)‐1‐phenylpenta‐1,4‐dien‐3‐ol 
• 129646-81-7 Acetic acid (E)-(R)-3-phenyl-1-vinyl-allyl ester 

Relevant articles and documents

Counteranion-controlled regioselectivity in palladium-catalyzed allylic amination of dienyl allylic carbonates

A regioselective Pd-catalyzed allylic amination reaction of dienyl allylic carbonates and aromatic amines has been developed by means of phosphoramidite-palladium catalysis. The regioselectivity could be altered by the counterion of the π-allylpalladium intermediate. As a result, either branched Z-dienyl allylic amines or linear conjugated allylic amines were generated in high levels of regioselectivity from the same substrates by tuning the reaction conditions.

Iridium-Catalyzed Asymmetric Allylic Alkylation of Deconjugated Butyrolactams

Compared with the ever-growing list of nonprochiral nucleophiles in Ir-catalyzed asymmetric allylic substitution reactions, prochiral nucleophiles are less studied. We present a new prochiral nucleophile, namely, deconjugated butyrolactam, for Ir-catalyze

Chiral naphthyl-C2-indole as scaffold for phosphine organocatalysis: Application in asymmetric formal [4 + 2] cycloaddition reactions

The applications of a newly designed chiral naphthyl-C2-indole bifunctional phosphine organocatalyst in stereoselective formal [4 + 2] cycloaddition reactions were reported. The chiral naphthyl-C2-indole skeleton was introduced to bifunctional phosphine o