218461-31-5

Basic information

• Product Name: 3-(2,4,6-trimethoxy-3,5-dimethyl-benzyloxy)-propan-1-ol
• CAS NO: 218461-31-5
• Molecular Weight: 284.353
• Mol File: 218461-31-5.mol

Chemical Properties

• CAS DataBase Reference: 3-(2,4,6-trimethoxy-3,5-dimethyl-benzyloxy)-propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2,4,6-trimethoxy-3,5-dimethyl-benzyloxy)-propan-1-ol(218461-31-5)
• EPA Substance Registry System: 3-(2,4,6-trimethoxy-3,5-dimethyl-benzyloxy)-propan-1-ol(218461-31-5)

Safety Data

• Hazardous Substances Data: 218461-31-5(Hazardous Substances Data)

Upstream product

• 95467-63-3 3,5-dimethyl-2,4,6-trimethoxybenzyl chloride 
• 504-63-2 trimethyleneglycol 

Downstream Products

• 218461-35-9 1-[3-(2,4,6-trimethoxy-3,5-dimethyl-benzyloxy)-propyl]-4-vinyloxy-azetidin-2-one 
• 218461-45-1 formic acid 4-oxo-1-[3-(2,4,6-trimethoxy-3,5-dimethyl-benzyloxy)-propyl]-azetidin-2-yl ester 
• 218461-41-7 trifluoro-methanesulfonic acid 3-(2,4,6-trimethoxy-3,5-dimethyl-benzyloxy)-propyl ester 

Relevant articles and documents

Synthesis of 1-oxacephams via improved cyclization of N-substituted-4- formyloxyazetidin-2-ones

The Lewis acid promoted cyclisation of N-substituted-4- formyloxyazetidin-2-ones, easily available from 4-vinyloxyazetidin-2-one is described. The efficiency of the ring closure reaction, to give 1-oxacephams, depends on the oxygen protected-activated group and the Lewis acid.