125783-05-3

Basic information

• Product Name: methyl (E)-2-pentyl-3-phenylprop-2-enoate
• Synonyms: methyl (E)-2-pentyl-3-phenylprop-2-enoate
• CAS NO: 125783-05-3
• Molecular Weight: 232.323
• Mol File: 125783-05-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: methyl (E)-2-pentyl-3-phenylprop-2-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (E)-2-pentyl-3-phenylprop-2-enoate(125783-05-3)
• EPA Substance Registry System: methyl (E)-2-pentyl-3-phenylprop-2-enoate(125783-05-3)

Safety Data

• Hazardous Substances Data: 125783-05-3(Hazardous Substances Data)

Upstream product

• 542-69-8 1-iodo-butane 
• 124957-36-4 Methyl 3-acetoxy-2-methylene-3-phenylpropanoate 
• 15676-66-1 tri-n-butylindium 

Downstream Products

• 15327-04-5 2-benzyl-heptanoic acid methyl ester 
• 109619-81-0 2-pentyl-3t-phenyl-acrylic acid 
• 1220187-74-5 (E)-2-benzylidene-N-methylheptanamide 

Relevant articles and documents

Organic reactions in water: An efficient zinc-mediated stereoselective synthesis of (E)- and (Z)-trisubstituted alkenes using unactivated alkyl halides

(Chemical Equation Presented) Treatment of the acetyl derivatives of the Baylis-Hillman adducts 3-hydroxy-2-methylene-alkanoates and 3-hydroxy-2- methylene-alkanenitriles with unactivated alkyl halides in the presence of Zn in saturated aqueous NH4/

ORGANIC COMPOUNDS

Disclosed are compounds having the ability to modulate, namely to improve, enhance and or modify fragrance compositions due to their ability to inhibit cytochrome P450 enzymes, e.g. CYP2A13 and CYP2B6.

Applications of the Baylis-Hillman Reaction 2: a Simple Stereoselective Synthesis of (E)- and (Z)-Trisubstituted Alkenes

Reaction of Grignard reagents with methyl 3-acetoxy-2-methylenealkanoates produces (2E)-2-substituted alk-2-enoates, whereas a similar reaction with 3-acetoxy-2-methylenealkanenitriles provides (2Z)-2-substituted alk-2-enenitriles in high (Z)-stereoselectivity.