128414-17-5

Basic information

• Product Name: (S)-4-<(Benzyloxycarbonyl)amino>tetrahydrofuran-2-ol
• Synonyms: (S)-4-<(Benzyloxycarbonyl)amino>tetrahydrofuran-2-ol
• CAS NO: 128414-17-5
• Molecular Weight: 237.255
• Mol File: 128414-17-5.mol

Chemical Properties

• CAS DataBase Reference: (S)-4-<(Benzyloxycarbonyl)amino>tetrahydrofuran-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4-<(Benzyloxycarbonyl)amino>tetrahydrofuran-2-ol(128414-17-5)
• EPA Substance Registry System: (S)-4-<(Benzyloxycarbonyl)amino>tetrahydrofuran-2-ol(128414-17-5)

Safety Data

• Hazardous Substances Data: 128414-17-5(Hazardous Substances Data)

Upstream product

• 87219-29-2 benzyl (3S)-5-oxotetrahydro-3-furanylcarbamate 

Downstream Products

• 128414-12-0 ((S)-2-[1,3]Dithiolan-2-yl-1-formyl-ethyl)-carbamic acid benzyl ester 
• 128414-15-3 [(2R,3S)-2-((R)-1-Hydroxy-ethyl)-5-methoxy-tetrahydro-furan-3-yl]-carbamic acid benzyl ester 
• 128414-16-4 ((2R,3R,4S)-3-Hydroxy-2-isobutyl-6-methoxy-tetrahydro-pyran-4-yl)-carbamic acid benzyl ester 
• 128414-13-1 ((1S,2R,3R)-1-[1,3]Dithiolan-2-ylmethyl-2,3-dihydroxy-butyl)-carbamic acid benzyl ester 
• 128414-14-2 ((1S,2R,3R)-1-[1,3]Dithiolan-2-ylmethyl-2,3-dihydroxy-5-methyl-hexyl)-carbamic acid benzyl ester 
• 174743-98-7 [(1S,3R)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-3-hydroxy-pent-4-enyl]-carbamic acid benzyl ester 
• 174848-54-5 [(1S,3S)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-3-hydroxy-pent-4-enyl]-carbamic acid benzyl ester 
• 1053271-26-3 C₂₈H₃₉NO₅SeSi 
• 128414-11-9 ((S)-2-[1,3]Dithiolan-2-yl-1-hydroxymethyl-ethyl)-carbamic acid benzyl ester 

Relevant articles and documents

New methodology for the synthesis of unsaturated 8-, 9- and 10-membered lactams

Unsaturated 8-, 9- and 10-membered medium ring lactams 1 (n = 1, 2, 3) have been prepared in good yield by the Claisen rearrangement of the vinyl-substituted precursors 3 in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU).

Stereoselective Synthesis of 3-Amino 1,2-Diols via Intermolecular Pinacol Cross-Coupling of α-Aldehydes with Aliphatic Aldehydes. Short Asymmetric Syntheses of Two 2,3,6-Trideoxy-3-amino Sugars

syn,syn-3-Amino 1,2-diols are prepared via a pinacol cross coupling reaction between N-Cbz- or N-Boc-α-amino aldehydes and aliphatic aldehydes.Application of this methodology to the synthesis of two amino sugars starting from N-Cbz-L-aspartic acid are described.