6304-96-7

Basic information

• Product Name: .alpha.-D-Glucopyranoside, methyl 6-deoxy-6-iodo-, triacetate
• Synonyms: .alpha.-D-Glucopyranoside, methyl 6-deoxy-6-iodo-, triacetate;Nsc43157
• CAS NO: 6304-96-7
• Molecular Formula: C₁₃H₁₉IO₈
• Molecular Weight: 430.19
• Mol File: 6304-96-7.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Density: 1.53g/cm³
• Refractive Index: 1.655
• CAS DataBase Reference: .alpha.-D-Glucopyranoside, methyl 6-deoxy-6-iodo-, triacetate(CAS DataBase Reference)
• NIST Chemistry Reference: .alpha.-D-Glucopyranoside, methyl 6-deoxy-6-iodo-, triacetate(6304-96-7)
• EPA Substance Registry System: .alpha.-D-Glucopyranoside, methyl 6-deoxy-6-iodo-, triacetate(6304-96-7)

Safety Data

• Hazardous Substances Data: 6304-96-7(Hazardous Substances Data)

Usage

General Description

.alpha.-D-Glucopyranoside, methyl 6-deoxy-6-iodo-, triacetate is a chemical compound that is a derivative of glucose. It is a white to off-white solid and is often used in organic synthesis and as a reagent in chemical reactions. The triacetate form of the compound makes it more stable and easier to handle in the laboratory. .alpha.-D-Glucopyranoside, methyl 6-deoxy-6-iodo-, triacetate is widely used in the production of pharmaceuticals, as well as in the research and development of new chemical compounds. Its specific properties and reactivity make it a valuable tool in organic chemistry and chemical synthesis.

InChI:InChI=1/C19H19BrN4O4S/c1-3-24-18(17(20)12-21-24)19(25)22-13-6-10-16(11-7-13)29(26,27)23-14-4-8-15(28-2)9-5-14/h4-12,23H,3H2,1-2H3,(H,22,25)

Upstream product

• 108-24-7 acetic anhydride 
• 97-30-3 methyl-alpha-D-glucopyranoside 

Downstream Products

• 24871-54-3 acetoxy α-D-2,3,4-triacetoxy-6-deoxy-6-iodoglucopyranoside 
• 4969-34-0 methyl 2,3,4-tri-O-acetyl-6-deoxy-6-nitro-α-D-glucopyranoside 
• 1623075-87-5 7-O-(1-O-methyl-2,3,4-tri-O-acetyl-6-deoxy-α-D-glicopyrane-6-yl)-genistein 
• 1623075-86-4 7,4'-di-O-(1-O-methyl-2,3,4-tri-O-acetyl-6-deoxy-α-D-glicopyrane-6-yl)-genistein 
• 1623075-91-1 7,4'-di-O-(1-O-methyl-6-deoxy-α-D-glicopyrane-6yl)-genistein 
• 1623075-89-7 7-O-(1-O-methyl-6-deoxy-α-D-glicopyrane-6-yl)-genistein 
• 87940-06-5 (2R,3S,4S,5S)-2,3,4-Tris-benzyloxy-5-hydroxy-cyclohexanone oxime 
• 87984-31-4 (2S,3R,4S,5R) 5-hydroxy-2,3,4-tris(benzyloxy) cyclohexane-1-one 
• 87940-07-6 (1S,2R,3R,4S,5R)-2,3,4-Tri-O-benzylcyclohexane-1,2,3,4,5-pentol 
• 87940-07-6 (1R,2R,3R,4S,5S)-2,3,4-Tri-O-benzylcyclohexane-1,2,3,4,5-pentol 
• 87940-07-6 (1R,2R,3R,4S,5R)-2,3,4-Tri-O-benzylcyclohexane-1,2,3,4,5-pentol 
• 87984-35-8 (2-L-1,3/2,4,5)-1-amino-2,3,4-tri-O-benzyl-2,3,4,5-cyclohexanetetrol 
• 87940-08-7 (2-L-1,2,4,5/3)-1-amino-2,3,4-tri-O-benzyl-2,3,4,5-cyclohexanetetrol 
• 85716-45-6 1L-(2,4,5/3)-2,3,4-Tri-O-benzyl-2,3,4,5-tetrahydroxy-1-cyclohexanon 

Relevant articles and documents

Calcium hypophosphite mediated deiodination in water: Mechanistic insights and applications in large scale syntheses of d-quinovose and d-rhamnose

The inorganic calcium hypophosphite was found to be a cheap, non-toxic, water-soluble and environmentally friendly reducing reagent for radical deiodination in water. Thorough mechanism studies revealed that calcium hypophosphite was oxidized to water insoluble calcium phosphite which was the major co-product of the deiodination reaction. Based on this observation, a practical synthesis of rare d-quinovose and d-rhamnose from cheap and commercially available materials on a hundred-mmol scale was reported.