125775-13-5

Basic information

• Product Name: 2-Propenoic acid, 3-[2-(1-pentenyl)phenyl]-, (E,Z)-
• CAS NO: 125775-13-5
• Molecular Formula: C14H16O2
• Molecular Weight: 216.28
• Mol File: 125775-13-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-Propenoic acid, 3-[2-(1-pentenyl)phenyl]-, (E,Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 3-[2-(1-pentenyl)phenyl]-, (E,Z)-(125775-13-5)
• EPA Substance Registry System: 2-Propenoic acid, 3-[2-(1-pentenyl)phenyl]-, (E,Z)-(125775-13-5)

Safety Data

• Hazardous Substances Data: 125775-13-5(Hazardous Substances Data)

Upstream product

• 141-82-2 malonic acid 
• 220903-35-5 (Z)-2-(pent-1-en-1-yl)benzaldehyde 
• 125775-12-4 3-<2-(1(Z)-pentenyl)phenyl>-2(E)-propenoic acid ethyl ester 
• 101-83-7 N-cyclohexyl-cyclohexanamine 
• 643-79-8 o-phthalic dicarboxaldehyde 
• 86867-62-1 (E)-3-(2-formylphenyl)propenoic acid ethyl ester 
• 110683-65-3 ((E)-2-Pent-1-enyl)-benzoic acid methyl ester 
• 128839-50-9 2-(1-Z-pentenyl)benzyl alcohol 
• 128839-49-6 methyl (Z)-2-(pent-1-en-1-yl)benzoate 
• 4122-56-9 methyl o-formylbenzoate 
• 378759-67-2 ethyl (E)-3-(2-iodophenyl)-2-propenoate 
• 5159-41-1 2-iodobenzyl alcohol 
• 26260-02-6 2-iodobenzaldehyde 
• 953391-26-9 ethyl E-2-(1-pentynyl)cinnamate 

Downstream Products

• 220903-36-6 3-(2-(1-Z-pentenyl)phenyl)-E-acrylic acid hydroxyazo benzotriazolyl ester 
• 147317-36-0 epi-pepticinnamin E 
• 125774-71-2 WS₉₃₂₆A 
• 147317-36-0 pepticinnamin E 

Relevant articles and documents

Concise synthesis of pentenyl phenyl acrylic acid

Pentenyl phenyl acrylic acid is a structural unit of pepticinnamin E, a natural product and a bisubstrate inhibitor of FPTase. In this article, a new synthetic strategy was developed to prepare pentenyl phenyl acrylic acid with high stereoselectivity and

Synthesis and in vitro evaluation of the Ras farnesyltransferase inhibitor pepticinnamin E

A modularly built bisubstrate inhibitor, the natural product pepticinnamin E (shown on the right) was synthesized for the first time. In the case of in vitro assays it inhibits the enzyme farnesyltransferase with respect to both the peptide substrate and farnesylpyrophosohate (K1 = 30 and 8 μM, respectively). The inhibitory activity is decisively influenced by the central tripeptide unit and the absolute configuration of the non-proteinogenic amino acid incorporated therein.

Structure of WS9326A, a Novel Tachykinin Antagonist from a Streptomyces

A novel tachykinin antagonist WS9326A was isolated from Streptomyces violaceoniger no. 9326.It is an acylated macrocyclic heptapeptide lactone consisting of L-Thr, (E)-dehydro-N-methyltyrosine ((E)-ΔMeTyr), L-Leu, D-Phe, L-allo-Thr, L-Asn, L-Ser, and 3-2