165874-25-9

Usage

Uses

Used in Pharmaceutical Industry:
.beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)is used as a potential pharmaceutical candidate for various applications due to its complex structure and the presence of multiple functional groups. These groups may allow for interactions with biopolymers and macromolecules, making it a promising compound for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, .beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)- can be used as a starting material or a model for studying the properties and reactivity of similar complex organic molecules. Understanding its behavior can contribute to the advancement of synthetic chemistry and the development of new compounds with specific applications.
Used in Material Science:
The unique structure of .beta.-D-Allopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)may also find applications in material science. Its properties could be exploited to create new materials with specific characteristics, such as improved stability, reactivity, or selectivity in various chemical processes.

Upstream product

• 85-44-9 phthalic anhydride 
• 165874-22-6 allyl 2-acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-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 
• 165874-19-1 allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-methanesulfonyl-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 165874-26-0 allyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-allopyranoside 
• 114853-35-9 allyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 65947-37-7 allyl 2-deoxy-2-acetamido-4,6-O-benzylidene-β-D-glucopyranoside 

Downstream Products

• 165874-29-3 C₅₈H₅₀Cl₃N₃O₁₃ 
• 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 
• 165874-28-2 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-allopyranose 
• 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 
• 165874-24-8 2,2,2-Trichloro-acetimidic acid (4aR,6S,7R,8S,8aS)-8-benzyloxy-7-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl ester 
• 165874-23-7 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-allopyranose 
• 165375-33-7 allyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-allopyranoside 
• 165375-32-6 prop-1-enyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-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.