1296671-54-9

Basic information

• Product Name: (2R,3R,4S)-3-(3,4,5-trimethoxybenzyl)-4-(3,4,5-trimethoxyphenyl)-2-((R)-4-ethyl-2-oxo-oxazolidin-3-yl)-3,4-dihydro-2H-pyran-6-carboxylic acid methyl ester
• Synonyms: (2R,3R,4S)-3-(3,4,5-trimethoxybenzyl)-4-(3,4,5-trimethoxyphenyl)-2-((R)-4-ethyl-2-oxo-oxazolidin-3-yl)-3,4-dihydro-2H-pyran-6-carboxylic acid methyl ester
• CAS NO: 1296671-54-9
• Molecular Weight: 601.651
• Mol File: 1296671-54-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3R,4S)-3-(3,4,5-trimethoxybenzyl)-4-(3,4,5-trimethoxyphenyl)-2-((R)-4-ethyl-2-oxo-oxazolidin-3-yl)-3,4-dihydro-2H-pyran-6-carboxylic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R,4S)-3-(3,4,5-trimethoxybenzyl)-4-(3,4,5-trimethoxyphenyl)-2-((R)-4-ethyl-2-oxo-oxazolidin-3-yl)-3,4-dihydro-2H-pyran-6-carboxylic acid methyl ester(1296671-54-9)
• EPA Substance Registry System: (2R,3R,4S)-3-(3,4,5-trimethoxybenzyl)-4-(3,4,5-trimethoxyphenyl)-2-((R)-4-ethyl-2-oxo-oxazolidin-3-yl)-3,4-dihydro-2H-pyran-6-carboxylic acid methyl ester(1296671-54-9)

Safety Data

• Hazardous Substances Data: 1296671-54-9(Hazardous Substances Data)

Upstream product

• 98974-04-0 (4R)-4-ethyl-1,3-oxazolidin-2-one 
• 121667-78-5 3-(3',4',5'-trimethoxyphenyl)propanal 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 59276-37-8 3,4,5-trimethoxybenzaldehyde dimethyl acetal 
• 20329-98-0 (E)-3,4,5-trimethoxy-cinnamic acid 
• 53560-26-2 3-(3,4,5-trimethoxyphenyl)propan-1-ol 
• 1296671-51-6 3-(3-(3,4,5-Trimethoxyphenyl)prop-1-(E)-enyl)-4-(R)-ethyloxazolidin-2-one 
• 162087-77-6 (E)-2-oxo-4-(3,4,5-trimethoxyphenyl)but-3-enoic acid methyl ester 

Relevant articles and documents

New two-step sequence involving a hetero-Diels-Alder and a nonphenolic oxidative coupling reaction: A convergent access to analogs of steganacin

A new family of analogs of steganacin, an important antimitotic compound, was accessed. It takes advantage of a completely stereoselective sequence of two key steps. The central dihydropyrane core is built by a highly diastereoselective and facially controlled hetero-Diels-Alder reaction. It is followed by a nonphenolic biaryl oxidative coupling with a complete atropo-stereoselectivity. It leads to a quick way to form cyclic biaryl lignans.