585-49-9

Basic information

• Product Name: Benzene, 1-(2-propenyloxy)-3-(trifluoromethyl)-
• CAS NO: 585-49-9
• Molecular Formula: C10H9F3O
• Molecular Weight: 202.176
• Mol File: 585-49-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(2-propenyloxy)-3-(trifluoromethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(2-propenyloxy)-3-(trifluoromethyl)-(585-49-9)
• EPA Substance Registry System: Benzene, 1-(2-propenyloxy)-3-(trifluoromethyl)-(585-49-9)

Safety Data

• Hazardous Substances Data: 585-49-9(Hazardous Substances Data)

Upstream product

• 98-17-9 3-Trifluoromethylphenol 
• 106-95-6 allyl bromide 

Downstream Products

• 98-17-9 3-Trifluoromethylphenol 
• 61761-32-8 5-fluoronaphthalen-1-ol 
• 1629184-55-9 2-(allyloxy)-1-propyl-4-(trifluoromethyl)benzene 
• 1629184-56-0 2-allyl-6-propyl-3-(trifluoromethyl)phenol 
• 902261-47-6 3-(3-trifluoromethyl-phenoxy)-propane-1,2-diol 
• 325-36-0 2-allyl-5-trifluoromethyl-anisole 
• 582-14-9 2-propyl-5-trifluoromethyl-anisole 
• 618-05-3 2-propyl-5-(trifluoromethyl)phenol 
• 448-36-2 2-methoxy-4-(trifluoromethyl)-benzoic acid 
• 585-43-3 2-allyl-5-trifluoromethyl phenol 
• 41389-17-7 2-allyl-5-(trifluoromethyl)phenol 

Relevant articles and documents

A mild and practical method for deprotection of aryl methyl/benzyl/allyl ethers with HPPh2andtBuOK

A general method for the demethylation, debenzylation, and deallylation of aryl ethers using HPPh2andtBuOK is reported. The reaction features mild and metal-free reaction conditions, broad substrate scope, good functional group compatibility, and high chemical selectivity towards aryl ethers over aliphatic structures. Notably, this approach is competent to selectively deprotect the allyl or benzyl group, making it a general and practical method in organic synthesis.

A transition-metal-free synthesis of fluorinated naphthols

Herein, we describe a transition-metal-free protocol for the conversion of simple 2-allyl-3-(trifluoromethyl)phenols into substituted 5-fluoronaphthalen-1- ols. The key events of this reaction include the selective activation of two C-F bonds and formatio

Process for the Preparation of Prostaglandin Analogues and Intermediates Thereof

The present application provides intermediates for preparing prostaglandin analogues and processes for preparing prostaglandin analogues and intermediates thereof. The intermediates include: A compound of formula (6): R1 represents H, C1-C5-alkyl, or benzyl, in particular isopropyl.