165874-22-6

Usage

Uses

Used in Pharmaceutical Industry:
.beta.-D-Allopyranoside, 2-propenyl 2-(acetylamino)-2-deoxy-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)is used as a potential pharmaceutical agent for its possible biological activity. The presence of a 2-deoxy sugar and various functional groups may contribute to its effectiveness in targeting specific biological pathways or interactions.
Used in Chemical Industry:
In the chemical industry, .beta.-D-Allopyranoside, 2-propenyl 2-(acetylamino)-2-deoxy-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)can be utilized as a building block or intermediate in the synthesis of more complex molecules. Its unique structure and functional groups make it a valuable component in the development of novel chemical compounds with specific properties and applications.
Used in Drug Delivery Systems:
.beta.-D-Allopyranoside, 2-propenyl 2-(acetylamino)-2-deoxy-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)may also be employed in the development of drug delivery systems, where its unique structure and functional groups can be leveraged to improve the delivery, bioavailability, and therapeutic outcomes of various pharmaceutical agents. This could involve the design of targeted drug carriers or the enhancement of drug solubility and stability.
Used in Research and Development:
.beta.-D-Allopyranoside, 2-propenyl 2-(acetylamino)-2-deoxy-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)can serve as a valuable research tool in the study of various biological processes and interactions. Its unique structure and functional groups may provide insights into the mechanisms of action of certain biological systems, leading to the discovery of new therapeutic targets or strategies.

Upstream product

• 165874-19-1 allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-methanesulfonyl-β-D-glucopyranoside 
• 65947-37-7 allyl 2-deoxy-2-acetamido-4,6-O-benzylidene-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 165874-21-5 allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-allopyranoside 

Downstream Products

• 165375-33-7 allyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-allopyranoside 
• 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 
• 165375-32-6 prop-1-enyl 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 
• 165874-25-9 allyl 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.