1279230-33-9

Basic information

• Product Name: 4-DEOXY-L-FUCOSE
• Synonyms: 4-DEOXY-L-FUCOSE
• CAS NO: 1279230-33-9
• Molecular Formula: C6H12O4
• Molecular Weight: 148.16
• Product Categories: 13C & 2H Sugars;aldehydes;Carbohydrates & Derivatives
• Mol File: 1279230-33-9.mol
• Article Data: 11

Chemical Properties

• Melting Point: 142-143°C
• Boiling Point: 281.0±40.0 °C(Predicted)
• Appearance: /
• Density: 1.366±0.06 g/cm3(Predicted)
• Storage Temp.: -20°C Freezer
• Solubility: Acetonitrile (Slightly), Methanol (Slightly)
• PKA: 12.54±0.70(Predicted)
• CAS DataBase Reference: 4-DEOXY-L-FUCOSE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-DEOXY-L-FUCOSE(1279230-33-9)
• EPA Substance Registry System: 4-DEOXY-L-FUCOSE(1279230-33-9)

Safety Data

• Hazardous Substances Data: 1279230-33-9(Hazardous Substances Data)

Usage

Chemical Properties

White Crystals

Uses

A potential inhibitor of fucosyltransferase

Upstream product

• 55338-33-5 methyl 4,6-dideoxy-α-D-arabino-hexopyranoside 
• 56733-83-6 1,3-bis(N-benzyloxycarbonyl)-spectinomycin 
• 174278-21-8 Imidazole-1-carbothioic acid O-[(3aS,4S,6R,7R,7aS)-4-methoxy-2,2-dimethyl-6-(toluene-4-sulfonyloxymethyl)-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yl] ester 
• 73635-99-1 methyl 2,3-O-isopropylidene-4-deoxy-α-D-lyxo-hexopyranoside 
• 144872-97-9 methyl 4,6-dideoxy-2,3-O-isopropylidene-α-D-lyxo-hexopyranoside 
• 20585-18-6 methyl 4,6-dideoxy-α-D-glucopyranoside 
• 132867-76-6 1,2,3-tri-O-benzoyl-6-deoxy-α-L-galactopyranose 
• 132867-78-8 1,2,3-tri-O-benzoyl-4,6-dideoxy-4-iodo-α-L-glucopyranose 
• 73-34-7 6-deoxy-L-galactose 
• 132867-80-2 1,2,3-tri-O-benzoyl-4,6-dideoxy-α-L-xylo-hexopyranose 
• 99944-94-2 2,3-anhydro-5-O-benzyl-1,6,7,8-tetradeoxy-L-galacto-oct-6-enitol 

Downstream Products

• 91273-90-4 (E)-(4R,5R,7R)-4,5,7-Trihydroxy-oct-2-enoic acid 2-(toluene-4-sulfonyl)-ethyl ester 
• 148406-82-0 2-(p-tolylsulfonyl)ethyl (2E,4S,5S,7R)-7-hydroxy-4,5-isopropylidenedioxy-2-octenoate 
• 133463-56-6 2-(p-tolylsulfonyl)ethyl (10E,4S,5S,7R,13S)-13-t-butyldimethylsiloxy-4,5-isopropylidenedioxy-7-methyl-9-oxo-8-oxa-10-tetradecenoate 
• 133522-16-4 2-(p-tolylsulfonyl)ethyl (10E,4S,5S,7R,13R)-13-t-butyldimethylsiloxy-4,5-isopropylidenedioxy-7-methyl-9-oxo-8-oxa-10-tetradecenoate 
• 133463-55-5 2-(p-Toluenesulfonyl)ethyl (4S,5S,7R)-7-hydroxy-(4,5-dimethylmethylene)dioxyoctanoate 
• 91273-91-5 p-toluenesulfonylethyl (4R,5R,7R,2E)-7-hydroxy-4,5-dimethylmethylenedioxy-2-octenoate 
• 133522-15-3 2-(p-tolylsulfonyl)ethyl (10E,4R,5R,7R,13S)-13-t-butyldimethylsiloxy-4,5-isopropylidenedioxy-7-methyl-9-oxo-8-oxa-10-tetradecenoate 
• 133522-14-2 2-(p-Toluenesulfonyl)ethyl (4R,5R,7R)-7-hydroxy-(4,5-dimethylmethylene)dioxyoctanoate 
• 91273-90-4 (E)-(4S,5S,7R)-4,5,7-Trihydroxy-oct-2-enoic acid 2-(toluene-4-sulfonyl)-ethyl ester 

Relevant articles and documents

PREPARATION OF O-1 - C-6 AND O-7 - C-14 FRAGMENTS OF COLLETODIOL

(5S,2E)-5-Tetrahydropyranyloxy-2-hexenoic acid and p-toluenesulfonylethyl (4R,5R,7R,2E)-7-hydroxy-4,5-dimethylmethylenedioxy-2-octenoate were prepared from ethyl acetoacetate and D-glucose, respectively.

Sugar-Pirating as an Enabling Platform for the Synthesis of 4,6-Dideoxyhexoses

An efficient divergent synthetic strategy that leverages the natural product spectinomycin to access uniquely functionalized monosaccharides is described. Stereoselective 2′- and 3′-reduction of key spectinomycin-derived intermediates enabled facile acces

Synthesis of the 4-, 6-deoxy, and 4,6-dideoxy derivatives of D-mannose

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