165874-19-1

Basic information

• Product Name: .beta.-D-Glucopyranoside, 2-propenyl 2-(acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-, 3-methanesulfonate
• Synonyms: .beta.-D-Glucopyranoside, 2-propenyl 2-(acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-, 3-methanesulfonate
• CAS NO: 165874-19-1
• Molecular Formula: C₁₉H₂₅NO₈S
• Molecular Weight: 427.47
• Mol File: 165874-19-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 668.8±55.0 °C(Predicted)
• Appearance: /
• Density: 1.34±0.1 g/cm3(Predicted)
• PKA: 13.60±0.70(Predicted)
• CAS DataBase Reference: .beta.-D-Glucopyranoside, 2-propenyl 2-(acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-, 3-methanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: .beta.-D-Glucopyranoside, 2-propenyl 2-(acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-, 3-methanesulfonate(165874-19-1)
• EPA Substance Registry System: .beta.-D-Glucopyranoside, 2-propenyl 2-(acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-, 3-methanesulfonate(165874-19-1)

Safety Data

• Hazardous Substances Data: 165874-19-1(Hazardous Substances Data)

Usage

Description

.beta.-D-Glucopyranoside, 2-propenyl 2-(acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-, 3-methanesulfonate is a chemical compound derived from glucopyranoside, a type of sugar. It is characterized by the presence of a propenyl group, an acetylamino group, and a methanesulfonate group. .beta.-D-Glucopyranoside, 2-propenyl 2-(acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-, 3-methanesulfonate has potential medicinal properties and is of interest in pharmaceutical research due to its unique chemical structure and possible effects on various biological processes.

Uses

Used in Pharmaceutical Research:
.beta.-D-Glucopyranoside, 2-propenyl 2-(acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-, 3-methanesulfonate is used as a research compound for studying its potential medicinal properties. Its unique structure allows for investigation into the relationship between sugar compounds and biological activity, which could lead to the development of new drugs.
Used in Anti-Inflammatory and Antibacterial Applications:
In the field of medicine, .beta.-D-Glucopyranoside, 2-propenyl 2-(acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-, 3-methanesulfonate is used as a potential anti-inflammatory or antibacterial agent. Its effects on various biological processes are being studied to determine its suitability for these applications.
Used in Drug Delivery Systems:
The methanesulfonate group in .beta.-D-Glucopyranoside, 2-propenyl 2-(acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-, 3-methanesulfonate may make it useful as a prodrug for targeted delivery of pharmaceutical agents. This application is being explored in the development of novel drug delivery systems to improve the efficacy and bioavailability of various medications.

Upstream product

• 65947-37-7 allyl 2-deoxy-2-acetamido-4,6-O-benzylidene-β-D-glucopyranoside 
• 124-63-0 methanesulfonyl chloride 

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 
• 165874-25-9 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 
• 165874-22-6 allyl 2-acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-β-D-allopyranoside 
• 151895-57-7 allyl 2,3-dideoxy-2,3-(N-p-toluenesulfonylepimino)-β-D-allopyranoside 
• 165874-21-5 allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-allopyranoside 

Relevant articles and documents

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.