6669-14-3

Basic information

• Product Name: Benzene, 1,1'-[(2-propenyloxy)methylene]bis-
• CAS NO: 6669-14-3
• Molecular Formula: C16H16O
• Molecular Weight: 224.302
• Mol File: 6669-14-3.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-[(2-propenyloxy)methylene]bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-[(2-propenyloxy)methylene]bis-(6669-14-3)
• EPA Substance Registry System: Benzene, 1,1'-[(2-propenyloxy)methylene]bis-(6669-14-3)

Safety Data

• Hazardous Substances Data: 6669-14-3(Hazardous Substances Data)

Upstream product

• 91-01-0 1,1-Diphenylmethanol 
• 107-18-6 allyl alcohol 
• 503-30-0 trimethylene oxide 
• 67-56-1 methanol 
• 1439-07-2 trans-Stilbene oxide 
• 908093-98-1 diazodiphenylmethane 
• 20907-32-8 sodium allyloxide 
• 90-99-3 diphenylchloromethane 
• 776-74-9 Bromodiphenylmethane 

Downstream Products

• 91-01-0 1,1-Diphenylmethanol 
• 119-61-9 benzophenone 
• 1337990-79-0 C₁₆H₁₆O 
• 5467-43-6 1,3,3-triphenylpropyne 
• 4286-85-5 4,4-diphenyl-1-butene 
• 6926-47-2 diphenylmethylazide 
• 101-81-5 Diphenylmethane 
• 6668-85-5 1-benzhydryloxy-3-piperidin-1-yl-propan-2-ol 
• 127022-64-4 C₂₁H₂₄O 
• 127022-57-5 C₂₁H₂₆O 
• 127022-59-7 C₂₁H₂₄O 
• 4165-79-1 1,1-diphenyl-3-buten-1-ol 
• 6669-15-4 <(diphenylmethoxy)methyl>oxirane 

Relevant articles and documents

Practical preparation of diphenylmethyl ethers from 2-diphenylmethoxypyridine using catalytic iron(III) chloride

A novel facile synthetic method for producing diphenylmethyl (DPM) ethers from 2-diphenylmethoxypyridine was developed. A variety of DPM ethers was successfully achieved with high yield via treatment of alcohols with 2-diphenylmethoxypyridine in the presence of catalytic FeCl3. The procedure is a practical and efficient synthetic procedure to protect various alcohols, and it can be applied to prepare bioactive compounds.

Boron Trifluoride?Diethyl Ether-Catalyzed Etherification of Alcohols: A Metal-Free Pathway to Diphenylmethyl Ethers

A novel boron trifluoride?diethyl ether (BF3?OEt2)-catalyzed etherification procedure has been developed in which primary and secondary alcohols are easily converted into diphenylmethyl ethers with yields of up to 99%.

Niobium(V) pentachloride: an efficient catalyst for C-, N-, O-, and S-nucleophilic substitution reactions of benzylic alcohols

Benzylic alcohols undergo easy C-, N-, O-, and S- centered nucleophilic substitution reactions with a catalytic amount of NbCl5.