57009-70-8

Basic information

• Product Name: 1,3-Dithiane, 2-(3,4,5-trimethoxyphenyl)-
• CAS NO: 57009-70-8
• Molecular Formula: C13H18O3S2
• Molecular Weight: 286.416
• Mol File: 57009-70-8.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 1,3-Dithiane, 2-(3,4,5-trimethoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dithiane, 2-(3,4,5-trimethoxyphenyl)-(57009-70-8)
• EPA Substance Registry System: 1,3-Dithiane, 2-(3,4,5-trimethoxyphenyl)-(57009-70-8)

Safety Data

• Hazardous Substances Data: 57009-70-8(Hazardous Substances Data)

Upstream product

• 109-80-8 1.3-propanedithiol 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 59276-37-8 3,4,5-trimethoxybenzaldehyde dimethyl acetal 

Downstream Products

• 828921-09-1 [2-(3,4,5-trimethoxy-phenyl)-[1,3]dithian-2-yl]-methanol 
• 89018-72-4 2-(3-hydroxy-4-methoxyphenyl)-1-(3,4,5-trimethoxyphenyl)ethan-1-one 
• 89064-44-8 5-[(2R)-2-hydroxy-2-(3,4,5-trimethoxyphenyl)ethyl]-2-methoxyphenol 
• 72690-16-5 (3S,4S)-4-(benzo[d][1,3]dioxol-5-ylmethyl)-3-(3,4,5-trimethoxybenzyl)dihydrofuran-2(3H)-one 
• 76236-34-5 (4S,5S)-4-(3,4,5-Trimethoxy-benzyl)-5-trityloxymethyl-dihydro-furan-2-one 
• 61038-90-2 (+)-stegane 
• 61038-90-2 (-)-isostegane 
• 41451-68-7 (+)-steganacin 
• 54094-07-4 4-chloro-3’,4’,5’-trimethoxybenzophenone 
• 26186-46-9 4-fluoro-3’,4’,5’-trimethoxybenzophenone 

Relevant articles and documents

Enantioselective Synthesis of a Furan Lignan (+)-Sylvone

A synthesis of natural tetrahydrofuran lignan (+)-sylvone is achieved starting from methyl allenoate in 5 steps. The synthesis begins from an enantioselective aldol reaction of methyl allenoate with 3,4-dimethoxybenzaldehyde to afford α-addition aldol add

Synthesis of 1,3-dithiane and 1,3-dithiolane derivatives by tungstate sulfuric acid: Recyclable and green catalyst

An efficient, novel, and environmentally benign procedure for the thioacetalization of aliphatic and aromatic carbonyl compounds in the presence of catalytic amounts of tungstate sulfuric acid under solvent-free conditions to afford 1,3-dithianes and 1,3-

Synthesis and cytotoxic activities of 4,5-diarylisoxazoles

A series of 4,5-diarylisoxazoles related to combretastatin A-4 (CA-4) were synthesized and evaluated for cytotoxicity against three human cancer cell lines. Among them, compound 6e showed better cytotoxic activity than CA-4 in HeLa and HepG2 cell lines as