2484-81-3

Basic information

• Product Name: methyl 2-O-acetyl-3-(acetylamino)-4,6-O-benzylidene-3-deoxyhexopyranoside
• CAS NO: 2484-81-3
• Molecular Formula: C₁₈H₂₃NO₇
• Molecular Weight: 365.3777
• Mol File: 2484-81-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 550.9°C at 760 mmHg
• Flash Point: 286.9°C
• Density: 1.28g/cm³
• Vapor Pressure: 3.51E-12mmHg at 25°C
• Refractive Index: 1.549
• CAS DataBase Reference: methyl 2-O-acetyl-3-(acetylamino)-4,6-O-benzylidene-3-deoxyhexopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-O-acetyl-3-(acetylamino)-4,6-O-benzylidene-3-deoxyhexopyranoside(2484-81-3)
• EPA Substance Registry System: methyl 2-O-acetyl-3-(acetylamino)-4,6-O-benzylidene-3-deoxyhexopyranoside(2484-81-3)

Safety Data

• Hazardous Substances Data: 2484-81-3(Hazardous Substances Data)

Usage

Description

Methyl 2-O-acetyl-3-(acetylamino)-4,6-O-benzylidene-3-deoxyhexopyranoside is a complex organic chemical compound that features a hexopyranoside ring with acetyl and benzylidene functional groups. methyl 2-O-acetyl-3-(acetylamino)-4,6-O-benzylidene-3-deoxyhexopyranoside is recognized for its potential as a versatile building block in the realms of organic synthesis and carbohydrate chemistry.

Uses

Used in Organic Synthesis:
Methyl 2-O-acetyl-3-(acetylamino)-4,6-O-benzylidene-3-deoxyhexopyranoside serves as a valuable building block in organic synthesis, allowing for the creation of a variety of complex molecules. Its unique structure provides a foundation for further chemical modifications and the development of new compounds with specific properties.
Used in Carbohydrate Chemistry:
In carbohydrate chemistry, this compound is utilized for studying the fundamental roles that carbohydrates play in biological systems. Its structure enables researchers to probe and understand carbohydrate interactions and functions within living organisms.
Used in Pharmaceutical Industry:
Methyl 2-O-acetyl-3-(acetylamino)-4,6-O-benzylidene-3-deoxyhexopyranoside holds promise in the pharmaceutical industry as a starting material for the synthesis of potential drug candidates. Its unique attributes may contribute to the development of novel therapeutic agents.
Used in Biotechnology:
Within the biotechnology sector, this compound can be employed as a tool for investigating carbohydrate-protein interactions, which are crucial in numerous biological processes. Understanding these interactions can lead to advancements in areas such as drug discovery and the design of bioactive molecules.
Further research is essential to fully explore the potential uses and properties of methyl 2-O-acetyl-3-(acetylamino)-4,6-O-benzylidene-3-deoxyhexopyranoside, expanding its applications across various scientific and industrial fields.

Upstream product

• 66537-92-6 methyl 2,3-anhydro-4,6-benzylidene-α-D-allopyranoside 
• 3162-96-7 4,6-O-benzylidene-1-O-methyl-α-D-glucopyranoside 
• 99745-99-0 methyl 3-amino-4,6-O-benzylidene-3-deoxy-α-D-glucopyranoside 
• 108-24-7 acetic anhydride 
• 134341-61-0 O²,O⁴-benzylidene-O³-(1-methoxy-2-oxo-ethyl)-erythrose 
• 101223-51-2 methyl 4,6-O-benzylidene-3-deoxy-3-phenylazo-α-D-glucopyranoside 
• 71184-15-1 methyl-3-deoxyamino-4,6-dioxabenzylidene-α-D-altropyranose 
• 3150-15-0 methyl 2,3-anhydro-4,6-O-benzilidene-α-D-mannopyranoside 
• 86420-78-2 methyl 2,3-anhydro-4,6-O-benzylidene-β-D-talopyranoside 
• 6748-86-3 methyl 4,6-O-benzylidene-β-D-galactopyranoside 2,3-di-O-p-toluenesulfonate 
• 3258-19-3 methyl-(2,3-anhydro-β-D-talopyranoside) 
• 71117-36-7 methyl 4,6-O-(S)-benzylidene-β-D-galactopyranoside 
• 35780-89-3 methyl-[O²-(toluene-4-sulfonyl)-β-D-galactopyranoside] 
• 86420-69-1 methyl 4,6-O-benzylidene-β-D-galactopyranoside 2-O-p-toluenesulfonate 

Downstream Products

• 2595-38-2 Methyl-(3-acetamino-3-deoxy-2,4,6-tri-O-acetyl-α-D-glucopyranosid) 
• 107650-89-5 methyl 3-acetamido-2-O-acetyl-3-deoxy-6-O-tosyl-α-D-glucopyranoside 
• 107741-02-6 (1S,2R,8S,8aR)-1,2,8-tris(benzyloxy)-octahydro-5-indolizinone 
• 107650-91-9 (2R,3S,4R)-1-acetyl-3,4-bis(benzyloxy)-2-<(1S)-1-benzyloxy-3-carboxypropyl>pyrrolidine 
• 107741-00-4 (2S,3S,4R)-1-acetyl-3,4-bis(benzyloxy)-2-<(1R)-1-benzyloxy-2,2-bis(ethylthio)ethyl>pyrrolidine 
• 107741-01-5 (2R,3S,4R)-1-acetyl-3,4-bis(benzyloxy)-2-<(1S)-1-benzyloxy-3-(ethoxycarbonyl)propyl>pyrrolidine 
• 107793-88-4 (2R,3S,4R)-1-acetyl-3,4-bis(benzyloxy)-2-<(1S,2E)-1-benzyloxy-3-ethoxycarbonyl-2-propenyl>pyrrolidine 
• 112533-90-1 methyl-[O²,O⁴-diacetyl-3-acetylamino-O⁶-(toluene-4-sulfonyl)-3-deoxy-α-D-altropyranoside] 
• 576-44-3 kanosamine 

Relevant articles and documents

Toward fluorinated aminoglycosides: Structural studies of phenylhydrazine condensation with carbohydrate derivatives

The reaction of phenylhydrazine with a sugar dialdehyde in water, as a key step for the synthesis of the 3-amino-3-deoxy-d-glucose moiety contained in kanamycin, has been revisited. Structural studies (IR and NMR as well as a simple theoretical model base