1392227-39-2

Basic information

• Product Name: (E)-iso-propyl 2-(3-n-butoxy-3-oxoprop-1-en-1-yl)-4-methoxybenzoate
• Synonyms: (E)-iso-propyl 2-(3-n-butoxy-3-oxoprop-1-en-1-yl)-4-methoxybenzoate
• CAS NO: 1392227-39-2
• Molecular Weight: 320.386
• Mol File: 1392227-39-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-iso-propyl 2-(3-n-butoxy-3-oxoprop-1-en-1-yl)-4-methoxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-iso-propyl 2-(3-n-butoxy-3-oxoprop-1-en-1-yl)-4-methoxybenzoate(1392227-39-2)
• EPA Substance Registry System: (E)-iso-propyl 2-(3-n-butoxy-3-oxoprop-1-en-1-yl)-4-methoxybenzoate(1392227-39-2)

Safety Data

• Hazardous Substances Data: 1392227-39-2(Hazardous Substances Data)

Upstream product

• 141-32-2 acrylic acid n-butyl ester 
• 6938-38-1 4-methoxy-benzoic acid isopropyl ester 

Relevant articles and documents

Oxidative alkenylation of aromatic esters by ruthenium-catalyzed twofold C-H bond cleavages

Cationic ruthenium(II) complexes enabled catalytic twofold C-H bond functionalizations with weakly coordinating aromatic esters in a highly chemo-, site- and diastereo-selective as well as site selective fashion. The oxidative Fujiwara-Moritani-type alkenylation provided step-economical access to diversely substituted styrenes and proved viable in an aerobic manner. Mechanistic studies were indicative of a reversible acetate-assisted cycloruthenation step.