828915-76-0

Basic information

• Product Name: INDEX NAME NOT YET ASSIGNED
• CAS NO: 828915-76-0
• Molecular Formula: C₉H₁₂O₄S
• Molecular Weight: 216.25
• Product Categories: METHYL
• Mol File: 828915-76-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: INDEX NAME NOT YET ASSIGNED(CAS DataBase Reference)
• NIST Chemistry Reference: INDEX NAME NOT YET ASSIGNED(828915-76-0)
• EPA Substance Registry System: INDEX NAME NOT YET ASSIGNED(828915-76-0)

Safety Data

• Hazardous Substances Data: 828915-76-0(Hazardous Substances Data)

Upstream product

• 1622-32-8 2-Chloroethanesulfonyl chloride 
• 445399-68-8 (2S)-2-(furan-2-yl)propan-1-ol 
• 828915-74-8 (S)-2-Bromo-1-furan-2-yl-ethanol 
• 828915-75-9 (R)-2-oxiranylfuran 
• 15109-94-1 1-(2-furyl)-2-bromoethanone 

Downstream Products

• 828915-81-7 (R)-2-{(3S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-3-[2-(dimethyl-phenyl-silanyl)-ethyl]-6-methylene-cyclohex-1-enyl}-propan-1-ol 
• 828915-82-8 ({2-[(1S,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-3-((R)-2-iodo-1-methyl-ethyl)-4-methylene-cyclohex-2-enyl]-ethyl}-dimethyl-silanyl)-benzene 
• 828915-84-0 (S)-4-{(3S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-3-[2-(dimethyl-phenyl-silanyl)-ethyl]-6-methylene-cyclohex-1-enyl}-pentanoic acid methyl ester 
• 828915-85-1 (S)-4-{(3S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-3-[2-(dimethyl-phenyl-silanyl)-ethyl]-6-methylene-cyclohex-1-enyl}-pentanoic acid 
• 828915-80-6 [(2-{6-(tert-butyl-dimethyl-silanyloxy)-3-[2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-4-methylene-cyclohex-2-enyl}-ethyl)-dimethyl-silanyl]-benzene 
• 828915-83-9 2-((S)-2-{(3S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-3-[2-(dimethyl-phenyl-silanyl)-ethyl]-6-methylene-cyclohex-1-enyl}-propyl)-malonic acid dimethyl ester 
• 828915-79-3 (1R,2S)-2-[2-(Dimethyl-phenyl-silanyl)-ethyl]-4-((R)-2-hydroxy-1-methyl-ethyl)-5-methylene-cyclohex-3-enol 

Relevant articles and documents

A concise sultone route to highly oxygenated 1,10-seco-eudesmanolides - enantioselective total synthesis of the antileukemic sesquiterpene lactones (-)-eriolanin and (-)-eriolangin

Using a sultone as the key intermediate, the first enantioselective total synthesis of the antileukemic 1,10-seco-eudesmanolides (-)-eriolanin (1) and (-)-eriolangin (2) was achieved, which also established the hitherto unknown absolute configuration of t

Enantioselective total synthesis of the highly oxygenated 1,10-seco-eudesmanolides eriolanin and eriolangin

Sultones of swing: A sultone served as the key intermediate in the first enantioselective total syntheses of the bioactive title compounds (see scheme), the absolute configuration of which is now established. Starting from 2-bromo-1-(2-furyl)ethanone, 24