254891-75-3

Basic information

• Product Name: 2-Furanmethanol, 5-ethynyltetrahydro-, (2R,5S)- (9CI)
• Synonyms: 2-Furanmethanol, 5-ethynyltetrahydro-, (2R,5S)- (9CI)
• CAS NO: 254891-75-3
• Molecular Formula: C₇H₁₀O₂
• Molecular Weight: 126.1531
• Mol File: 254891-75-3.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Furanmethanol, 5-ethynyltetrahydro-, (2R,5S)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Furanmethanol, 5-ethynyltetrahydro-, (2R,5S)- (9CI)(254891-75-3)
• EPA Substance Registry System: 2-Furanmethanol, 5-ethynyltetrahydro-, (2R,5S)- (9CI)(254891-75-3)

Safety Data

• Hazardous Substances Data: 254891-75-3(Hazardous Substances Data)

Upstream product

• 936915-96-7 tert-butyl-(5-ethynyl-tetrahydro-furan-2-ylmethoxy)-diphenyl-silane 
• 113730-85-1 (S)-1-((R)-1,4-dioxaspiro[4.5]decan-2-yl)pent-4-en-1-ol 
• 936924-59-3 [5-(1,4-dioxa-spiro[4.5]dec-2-yl)-tetrahydro-furan-2-yl]-methanol 
• 936915-95-6 5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-2-carbaldehyde 
• 936915-83-2 benzoic acid 1-(1,4-dioxa-spiro[4.5]dec-2-yl)-pent-4-enyl ester 
• 936915-94-5 1-[5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-ethane-1,2-diol 
• 936915-91-2 benzoic acid 1-(1,4-dioxa-spiro[4.5]dec-2-yl)-4,5-dihydroxy-pentyl ester 
• 254891-63-9 (3S,6S)-3-acetoxy-6,7-(isopropylidenedioxy)hept-1-yne 
• 254891-64-0 (3S,6S)-3-acetoxy-6,7-dihydroxyhept-1-yne 
• 254891-61-7 (2R,3S,6S)-1-chloro-2,3-epoxy-6,7-(isopropylidenedioxy)heptane 
• 254891-62-8 (3S,6S)-3-hydroxy-6,7-(isopropylidenedioxy)hept-1-yne 
• 161954-37-6 ethyl (2E,6S)-6,7-(isopropylidenedioxy)hept-2-enoate 
• 161954-38-7 (2E,6S)-6,7-(isopropylidenedioxy)hept-2-en-1-ol 
• 161954-39-8 (2S,3S,6S)-2,3-epoxy-6,7-(isopropylidenedioxy)heptan-1-ol 

Downstream Products

• 254891-76-4 (2R,5S)-cis-5-ethynyl-2-[(p-toluenesulfonyloxy)methyl]tetrahydrofuran 

Relevant articles and documents

(R)-2,3-Cyclohexylideneglyceraldehyde: a novel template for simple entry into both cis- and trans-2,5-disubstituted tetrahydrofurans

Sharpless asymmetric dihydroxylation at the terminal olefin of benzoates 3a and 3b, using both AD-mix α and AD-mix β afforded only one diastereomer of diols 5a and 5b, respectively. Diols 5a and 5b were easily transformed into cis- and trans-2,5-disubstit