140705-14-2

Basic information

• Product Name: 2-(3-methoxy-2-propoxy-5-((2S,5S)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran-2-yl)phenylsulfonyl)ethanol
• Synonyms: 2-(3-methoxy-2-propoxy-5-((2S,5S)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran-2-yl)phenylsulfonyl)ethanol;(2S,5S)-2-[3-[[2-[(tert-Butyldimethylsilyl)oxy]ethyl]sulfonyl]-5-methoxy-4-propoxyphenyl]-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran
• CAS NO: 140705-14-2
• Molecular Formula: C₃₁H₄₈O₉SSi
• Molecular Weight: 624.86
• Mol File: 140705-14-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 683.572°C at 760 mmHg
• Flash Point: 367.211°C
• Appearance: /
• Density: 1.114
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.508
• CAS DataBase Reference: 2-(3-methoxy-2-propoxy-5-((2S,5S)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran-2-yl)phenylsulfonyl)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-methoxy-2-propoxy-5-((2S,5S)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran-2-yl)phenylsulfonyl)ethanol(140705-14-2)
• EPA Substance Registry System: 2-(3-methoxy-2-propoxy-5-((2S,5S)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran-2-yl)phenylsulfonyl)ethanol(140705-14-2)

Safety Data

• Hazardous Substances Data: 140705-14-2(Hazardous Substances Data)

Usage

Methoxy group

Presence indicates potential solubility and lipophilicity.

Propoxy group

Presence indicates potential solubility and lipophilicity.

Phenyl group

Contributes to the compound's structure and stability.

Tetrahydrofuran ring

Adds structural complexity and may have applications in drug development or material science.

Sulfonyl group

Indicates the presence of a sulfonated phenyl compound.

Ethanol group

Contributes to the compound's structure and stability.

Structural complexity

Suggests potential for pharmaceutical or industrial applications, such as drug development, material science, or chemical synthesis.

InChI:InChI=1/C31H48O9SSi/c1-11-14-38-30-27(36-7)19-22(20-28(30)41(32,33)16-15-39-42(9,10)31(2,3)4)24-13-12-23(40-24)21-17-25(34-5)29(37-8)26(18-21)35-6/h17-20,23-24H,11-16H2,1-10H3/t23-,24-/m0/s1

Upstream product

• 2675-79-8 1-bromo-3,4,5-trimethoxybenzene 
• 81952-68-3 1-lithio-3,4,5-trimethoxybenzene 
• 141869-80-9 (S)-5-{3-[2-(tert-Butyl-dimethyl-silanyloxy)-ethanesulfonyl]-5-methoxy-4-propoxy-phenyl}-dihydro-furan-2-one 
• 140705-18-6 (S)-5-[3-(2-Hydroxy-ethylsulfanyl)-5-methoxy-4-propoxy-phenyl]-dihydro-furan-2-one 
• 133095-92-8 4-(3-Iodo-5-methoxy-4-propoxy-phenyl)-4-oxo-butyric acid tert-butyl ester 
• 133095-94-0 (S)-4-Hydroxy-4-(3-iodo-5-methoxy-4-propoxy-phenyl)-butyric acid 
• 133095-95-1 4[3-Methoxy-4-n-propyloxy-5-iodophenyl]-4S-butyrolactone 
• 481725-17-1 (1R,2S,3S,5S,6R,7S)-4,10-dioxa-3-[3-methoxy-5-(2'-t-butyldimethylsilyloxyethanesulfanyl)-4-propoxy]-5-[(3',4',5')-trimethoxyphenyl]-tricyclo[5.2.1.0^2,6]dec-8-en-3-ol 
• 481725-18-2 (1R,2S,3S,5S,6R,7S)-4,10-dioxa-3-[3-methoxy-5-(2'-t-butyldimethylsilyloxyethanesulfanyl)-4-propoxy]-5-[(3',4',5')-trimethoxyphenyl]-tricyclo[5.2.1.0^2,6]dec-8-ene 
• 481725-19-3 (2S,5S)-2-(3',4',5'-trimethoxyphenyl)-5-[3-methoxy-5-(2'-t-butyldimethylsilyloxyethanesulfanyl)-4-propoxyphenyl]-2,5-dihydrofuran 
• 481725-15-9 (S)-((1S,2S,3R,4R)-3-Hydroxymethyl-7-oxa-bicyclo[2.2.1]hept-5-en-2-yl)-(3,4,5-trimethoxy-phenyl)-methanol 
• 481725-11-5 1-bromo-3-methoxy-4-propoxy-5-(2'-tert-butyldimethylsilyloxyethanesulfanyl)benzene 
• 481725-16-0 (1R,2S,5S,6R,7S)-5-[(3',4',5')-trimethoxyphenyl]-4,10-dioxatricyclo[5.2.1.0^2,6]dec-8-en-3-one 
• 481725-13-7 1-bromo-3-methoxy-4-propoxy-5-(2'-hydroxyethanesulfanyl)benzene 

Downstream Products

• 135947-75-0 MK 287 

Relevant articles and documents

Enantioselective synthesis of the PAF antagonist MK-287

Following a general method of synthesis of optically active 2,5-disubstituted tetrahydrofurans, an enantioselective synthesis of the PAF antagonist, MK-287 is described.