445399-68-8

Basic information

• Product Name: (2S)-2-(furan-2-yl)propan-1-ol
• Synonyms: (2S)-2-(furan-2-yl)propan-1-ol
• CAS NO: 445399-68-8
• Molecular Weight: 126.155
• Mol File: 445399-68-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S)-2-(furan-2-yl)propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-2-(furan-2-yl)propan-1-ol(445399-68-8)
• EPA Substance Registry System: (2S)-2-(furan-2-yl)propan-1-ol(445399-68-8)

Safety Data

• Hazardous Substances Data: 445399-68-8(Hazardous Substances Data)

Upstream product

• 445399-67-7 (R)-1-((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-2-furan-2-yl-propan-1-one 
• 132819-58-0 2-(furan-2-yl)propan-1-ol 
• 240801-32-5 vinyl 3-(4-methylphenyl)propanoate 

Downstream Products

• 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 
• 828915-80-6 [(2-{6-(tert-butyl-dimethyl-silanyloxy)-3-[2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-4-methylene-cyclohex-2-enyl}-ethyl)-dimethyl-silanyl]-benzene 
• 828915-85-1 (S)-4-{(3S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-3-[2-(dimethyl-phenyl-silanyl)-ethyl]-6-methylene-cyclohex-1-enyl}-pentanoic acid 
• 828915-84-0 (S)-4-{(3S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-3-[2-(dimethyl-phenyl-silanyl)-ethyl]-6-methylene-cyclohex-1-enyl}-pentanoic acid methyl ester 
• 828915-82-8 ({2-[(1S,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-3-((R)-2-iodo-1-methyl-ethyl)-4-methylene-cyclohex-2-enyl]-ethyl}-dimethyl-silanyl)-benzene 
• 828915-81-7 (R)-2-{(3S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-3-[2-(dimethyl-phenyl-silanyl)-ethyl]-6-methylene-cyclohex-1-enyl}-propan-1-ol 
• 828915-79-3 (1R,2S)-2-[2-(Dimethyl-phenyl-silanyl)-ethyl]-4-((R)-2-hydroxy-1-methyl-ethyl)-5-methylene-cyclohex-3-enol 
• 828915-76-0 (1S,2S,6S,8R)-2-Methyl-4,11-dioxa-5-thia-tricyclo[6.2.1.0^1,6]undec-9-ene 5,5-dioxide 

Relevant articles and documents

Enzymatic kinetic resolution of 1-(3′-furyl)-3-buten-1-ol and 2-(2′-furyl)-propan-1-ol

The enzymatic kinetic resolution of the racemic alcohols 1-(3′-furyl)-3-buten-1-ol (±)-1 and 2-(2′-furyl)propan-1-ol (±)-2 was investigated by screening a range of lipases and esterases for enantioselective transacylation, as well as for enantioselective hydrolysis. For both alcohols, lipase-catalyzed hydrolysis of the derived racemic acetate gave the best results for accessing the desired (S)-enantiomers. In the case of the secondary alcohol (±)-1, ASL turned out to be the optimum enzyme, whereas PPL was found to be superior in the case of the primary alcohol (±)-2. Additionally, an alternative access to (S)-2 via Oppolzer's camphor sultam methodology is described.