165874-28-2

Usage

Uses

Used in Organic Chemistry:
.beta.-D-Allopyranose, 2-deoxy-4-O-2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)-.beta.-D-allopyranosyl-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3,6-bis-O-(phenylmethyl)is used as a complex carbohydrate derivative for various organic synthesis processes due to its unique structure and potentially diverse reactivity.
Used in Pharmaceutical Industry:
.beta.-D-Allopyranose, 2-deoxy-4-O-2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)-.beta.-D-allopyranosyl-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3,6-bis-O-(phenylmethyl)is used as a potential candidate for drug development in the pharmaceutical industry, given its unique structure and the possibility of diverse reactivity.
Used in Materials Science:
.beta.-D-Allopyranose, 2-deoxy-4-O-2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)-.beta.-D-allopyranosyl-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3,6-bis-O-(phenylmethyl)is used as a potential building block for the development of novel materials in materials science, taking advantage of its complex structure and functional groups.

Upstream product

• 165375-33-7 allyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-allopyranoside 
• 165874-26-0 allyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-allopyranoside 
• 165874-21-5 allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-allopyranoside 
• 165874-20-4 allyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-3-O-trifluoromethanesulfonyl-β-D-glucopyranoside 
• 165375-32-6 prop-1-enyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-allopyranoside 
• 165874-25-9 allyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-allopyranoside 
• 165874-23-7 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-allopyranose 
• 165874-19-1 allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-methanesulfonyl-β-D-glucopyranoside 
• 165874-22-6 allyl 2-acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-β-D-allopyranoside 
• 114853-35-9 allyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 65947-37-7 allyl 2-deoxy-2-acetamido-4,6-O-benzylidene-β-D-glucopyranoside 
• 85-44-9 phthalic anhydride 
• 165874-27-1 allyl 3,6-di-O-benzyl-4-O-(3-O-benzyl-4,6-benzylidene-2-deoxy-2-phthalimido-β-D-allopyranosyl)-2-deoxy-2-phthalimido-β-D-allopyranoside 

Downstream Products

• 165874-29-3 C₅₈H₅₀Cl₃N₃O₁₃ 
• 158528-74-6 (1S,5S)-3-dimethylamino-8-exo-hydroxymethyl-7-endo-hydroxy-2-oxa-4-azabicyclo<3.3.0>oct-3-en-6-endo-yl 2-acetamido-4-O-(2-acetamido-2-deoxy-β-D-allopyranosyl)-2-deoxy-β-D-allopyranoside 

Relevant academic research and scientific papers

Syntheses of the Fungicide/Insecticide Allosamidin and a Structural Isomer

A synthesis of the naturally occurring inhibitor of chitin metabolism, allosamidin 1, involves, as the key step, condensation between the allosamizoline derivative 39, prepared following oxyamination of the cyclopentene 19, and the disaccharide glycosylating agent 54 which was synthesised from 2-acetamido-2-deoxy-D-glucose.The structural isomer 59 of allosamidin is also reported.Brief biological test results obtained using isomers 1 and 59 are recorded.