4646-99-5

Basic information

• Product Name: 3-Cinnamyloxy-methoxy-benzol
• Synonyms: 3-Cinnamyloxy-methoxy-benzol
• CAS NO: 4646-99-5
• Molecular Weight: 240.302
• Mol File: 4646-99-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-Cinnamyloxy-methoxy-benzol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Cinnamyloxy-methoxy-benzol(4646-99-5)
• EPA Substance Registry System: 3-Cinnamyloxy-methoxy-benzol(4646-99-5)

Safety Data

• Hazardous Substances Data: 4646-99-5(Hazardous Substances Data)

Upstream product

• 150-19-6 O-methylresorcine 
• 4392-24-9 3-bromo-1-phenyl-1-propenyl bromide 
• 2687-12-9 cinnamyl chloride 

Downstream Products

• 1393362-06-5 2-cinnamyl-5-methoxyphenol 
• 1393362-04-3 4-methoxy-1-(1-phenylallyl)-2-(vinyloxy)benzene 
• 1393362-05-4 4-phenyl-7-methoxy-4H-chromene 
• 4647-01-2 5-methoxy-2-(1-phenylallyl)phenol 
• 300-57-2 allylbenzene 

Relevant articles and documents

From precursor to catalyst: The involvement of [Ru(η5- Cp*)Cl2]2 in highly branch selective allylic etherification of cinnamyl chlorides

(RuCp*Cl2)2, a general entry into Cp*Ru sandwich and half-sandwich chemistry was first used as a precatalyst in allylic etherification of cinnamyl chlorides with up to 98:2 regioselectivity (19 examples). Both the solvent effect and the exsiccant reaction condition are crucial to the reactivity and selectivity. Preliminary mechanism studies and the demonstration of Fluoxetine synthesis were presented in this work as well.