88842-13-1

Basic information

• Product Name: 2-Pentenoic acid, 5-phenyl-, ethyl ester, (Z)-
• CAS NO: 88842-13-1
• Molecular Formula: C13H16O2
• Molecular Weight: 204.269
• Mol File: 88842-13-1.mol
• Article Data: 29

Chemical Properties

• CAS DataBase Reference: 2-Pentenoic acid, 5-phenyl-, ethyl ester, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pentenoic acid, 5-phenyl-, ethyl ester, (Z)-(88842-13-1)
• EPA Substance Registry System: 2-Pentenoic acid, 5-phenyl-, ethyl ester, (Z)-(88842-13-1)

Safety Data

• Hazardous Substances Data: 88842-13-1(Hazardous Substances Data)

Upstream product

• 104-53-0 3-phenyl-propionaldehyde 
• 4083-85-6 triphenyl(carbethoxymethyl)phosphonium bromide 
• 121192-49-2 P--P,P-diphenyl-P-methylphosphonium trifluoromethanesulfonate 
• 1099-45-2 ethyl (triphenylphosphoranylidene)acetate 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 100-52-7 benzaldehyde 
• 250607-16-0 3-(1'-hydroxy-3'-phenylpropyl)-5,5-dimethyloxazolidin-2-one 
• 508230-18-0 C₂₂H₁₅F₁₂O₄P 
• 250607-11-5 3-(3'-phenylpropionyl)-5,5-dimethyloxazolidin-2-one 
• 13950-58-8 ethyl 2-(triphenylsilyl)acetate 
• 16139-79-0 ethyl diphenylphosphonoacetate 
• 1071-46-1 hydrogen ethyl malonate 
• 122-97-4 3-Phenyl-1-propanol 
• 188945-44-0 ethyl 2-[bis(2-isopropylphenoxy)phosphoryl]acetate 

Downstream Products

• 112087-56-6 (2Z)-5-phenylpent-2-enal 
• 1198356-01-2 (R)-ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-phenylpentanoate 
• 182417-58-9 (R)-3-hydroxy-5-phenyl-pentanoic acid ethyl ester 
• 88842-06-2 Toluene-4-sulfonic acid (2S,3R)-3-hydroxy-2-methoxy-5-phenyl-pentyl ester 
• 88853-99-0 (2R,3S)-2-Methoxy-5-phenyl-1-(tetrahydro-pyran-2-yloxy)-pentan-3-ol 
• 88842-14-2 (2S,3R)-5-Phenyl-1-(tetrahydro-pyran-2-yloxy)-pentane-2,3-diol 
• 344889-82-3 2-((Z)-5-Phenyl-pent-2-enyloxy)-tetrahydro-pyran 
• 88842-05-1 (2S,3R)-2-Methoxy-5-phenyl-pentane-1,3-diol 
• 74824-85-4 (2S,3R)-3-Methoxy-2-phenethyl-oxetane 
• 134420-94-3 ethyl 3-(benzylamino)-5-phenylvalerate 
• 138034-94-3 (Z)-5-Phenylpent-2-enoic Acid 
• 39520-63-3 (Z)-5-phenylpent-2-en-1-ol 

Relevant articles and documents

Essential structural features of (2Z,4E)-5-phenylpenta-2,4-dienoic acid for inhibition of root gravitropism

Previously, we found (2Z,4E)-5-phenylpenta-2,4-dienoic acid (ku-76) to be a selective inhibitor of root gravitropic bending of lettuce radicles at 5 μM, with no concomitant growth inhibition. Here, we describe a structure-activity relationship study of ku

Facile synthesis of α, β-unsaturated esters through a one-pot copper-catalyzed aerobic oxidation-Wittig reaction

An efficient one-pot synthesis of α, β-unsaturated esters through the aerobic oxidation – Wittig tandem reaction of alcohols and phosphorous ylide is developed. This new method operates under mild reaction conditions, and uses CuI/TEMPO (TEMPO = 2,2,6,6-tetramethylpiperidine-N-oxyl) as co-catalyst and air (O2) as the oxidant. It tolerates a wide range of functionalized benzylic alcohol and aliphatic alcohols.

Molybdenum-Catalyzed Stereospecific Deoxygenation of Epoxides to Alkenes

Mild and simple catalytic systems consisting of molybdenum(VI) dichloride dioxide [MoO2Cl2] as a catalyst and a phosphine as reductant have been developed for the stereospecific deoxygenation of epoxides to alkenes. The reactions using 1,2-bis(diphenylphosphino)ethane (dppe) and triphenylphosphine (PPh3) proceed with retention and inversion of stereochemistry, respectively. The mild reaction tolerates the presence of various functional groups and affords stereodefined substituted olefins in good yields. (Figure presented.).