6027-62-9

Basic information

• Product Name: 3-deoxy-3-iodo-1,2:5,6-di-O-isopropylidene-α-D-allofuranose
• CAS NO: 6027-62-9
• Molecular Weight: 370.184
• Mol File: 6027-62-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-deoxy-3-iodo-1,2:5,6-di-O-isopropylidene-α-D-allofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 3-deoxy-3-iodo-1,2:5,6-di-O-isopropylidene-α-D-allofuranose(6027-62-9)
• EPA Substance Registry System: 3-deoxy-3-iodo-1,2:5,6-di-O-isopropylidene-α-D-allofuranose(6027-62-9)

Safety Data

• Hazardous Substances Data: 6027-62-9(Hazardous Substances Data)

Upstream product

• 80667-81-8 1,2:5,6-di-O-isopropylidene-3-O-(N-imidazole-1-sulfonyl)-α-D-glucofuranose 

Downstream Products

• 13265-86-6 3-S-Benzyl-1,2:5,6-di-O-isopropyliden-3-thio-α-D-glucose 
• 16848-19-4 3-amino-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-glucofuranoside 
• 108380-26-3 Methyl 6-O-benzyl-3,5-dideoxy-2-methylthiocarbonyl (α- and β-)-D-erythrohexofuranoside 
• 108380-25-2 Methyl 6-O-benzyl-3,5-dideoxy-(α- and β-)-D-erythrohexofuranoside 
• 108380-27-4 Methyl 6-O-benzyl-2,3,5-trideoxy-(α,β)-D-glycerohexofuranoside 
• 108380-24-1 6-O-Benzyl-3,5-dideoxy-1,2-O-isopropylidene-α-D-erythro-hexofuranose 
• 108380-28-5 (S)-5-(2-(benzyloxy)ethyl)dihydrofuran-2(3H)-one 
• 108380-29-6 (S)-5-(2-Benzyloxy-ethyl)-tetrahydro-furan-2-ol 
• 16848-19-4 3-amino-3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 81645-66-1 3-benzamido-3-deoxy-1,2-O-isopropylidene-α-D-glucofuranose 3,5,6-N,O,O-bicyclophosphite 
• 81645-61-6 3-benzamido-3-deoxy-1,2-O-isopropylidene-α-D-glucofuranose 
• 81645-62-7 3-Benzamido-3-desoxy-1,2;5,6-di-O-isopropyliden-α-D-glucofuranose 
• 107690-56-2 (1R,5R)-6-acetyl-2-oxa-6-azabicyclo<3.3.0>octan-3-one 
• 197302-50-4 Toluene-4-sulfonic acid (R)-2-((3aR,5R,6S,6aS)-6-diethylthiocarbamoylsulfanyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-2-hydroxy-ethyl ester 

Relevant articles and documents

Design and reactivity of organic functional groups - Preparation and nucleophilic displacement reactions of imidazole-1-sulfonates (imidazylates)

Imidazole-1-sulfonate, a new type of leaving group by remote activation, allows facile S(N)2 substitution reactions at sterically crowded centers with various nucleophiles under mild conditions. It could be easily prepared from alcohols with cheap reagent