849938-20-1

Basic information

• Product Name: Phenyl 3,4-Di-O-acetyl-α-O-benzyl-1-thio-α-L-rhamnopyranoside
• Synonyms: Phenyl 3,4-Di-O-acetyl-α-O-benzyl-1-thio-α-L-rhamnopyranoside;Phenyl 6-Deoxy-2-O-(phenylMethyl)-1-thio-α-L-Mannopyranoside Diacetate
• CAS NO: 849938-20-1
• Molecular Formula: C₂₃H₂₆O₆S
• Molecular Weight: 430.51394
• Product Categories: 13C & 2H Sugars;Carbohydrates & Derivatives;Sulfur & Selenium Compounds
• Mol File: 849938-20-1.mol
• Article Data: 2

Chemical Properties

• Melting Point: 95-97?C
• Appearance: /
• Solubility: Dichloromethane, Ethyl Acetate, Methanol
• CAS DataBase Reference: Phenyl 3,4-Di-O-acetyl-α-O-benzyl-1-thio-α-L-rhamnopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Phenyl 3,4-Di-O-acetyl-α-O-benzyl-1-thio-α-L-rhamnopyranoside(849938-20-1)
• EPA Substance Registry System: Phenyl 3,4-Di-O-acetyl-α-O-benzyl-1-thio-α-L-rhamnopyranoside(849938-20-1)

Safety Data

• Hazardous Substances Data: 849938-20-1(Hazardous Substances Data)

Usage

Description

Phenyl 3,4-Di-O-acetyl-α-O-benzyl-1-thio-α-L-rhamnopyranoside is a complex organic compound characterized by its unique molecular structure. It is a glycoside derivative, featuring a phenyl group, acetyl groups, a benzyl group, and a thio-linked rhamnopyranoside moiety. Phenyl 3,4-Di-O-acetyl-α-O-benzyl-1-thio-α-L-rhamnopyranoside is known for its potential applications in various fields, particularly in organic synthesis, due to its versatile chemical properties.

Uses

Used in Organic Synthesis:
Phenyl 3,4-Di-O-acetyl-α-O-benzyl-1-thio-α-L-rhamnopyranoside is used as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure allows for selective reactions and modifications, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Phenyl 3,4-Di-O-acetyl-α-O-benzyl-1-thio-α-L-rhamnopyranoside is used as a precursor for the synthesis of bioactive compounds. Its ability to form glycosidic linkages with other molecules makes it a promising candidate for the development of new drugs with improved pharmacological properties, such as enhanced solubility, stability, and bioavailability.
Used in Agrochemical Industry:
Phenyl 3,4-Di-O-acetyl-α-O-benzyl-1-thio-α-L-rhamnopyranoside also finds applications in the agrochemical industry, where it is used as a starting material for the synthesis of novel agrochemicals. Its potential to be modified and functionalized allows for the development of new pesticides, herbicides, and other agrochemicals with improved efficacy and selectivity.
Used in Research and Development:
In the field of research and development, Phenyl 3,4-Di-O-acetyl-α-O-benzyl-1-thio-α-L-rhamnopyranoside serves as a valuable tool for studying the synthesis and properties of complex organic molecules. Its unique structure and reactivity make it an ideal candidate for exploring new reaction pathways, catalysts, and synthetic strategies, ultimately contributing to the advancement of organic chemistry.

Upstream product

• 849938-16-5 phenyl 2-O-benzyl-1-thio-α-L-rhamnopyranoside 
• 108-24-7 acetic anhydride 

Downstream Products

• 77307-50-7 Kaempferol-3-O-(3,4-O-diacetyl-α-L-rhamnopyranoside) 
• 849938-27-8 5,7-bis(benzyloxy)-2-(4-benzyloxyphenyl)-3-[3,4-di-O-acetyl-2-O-benzyl-α-L-rhamnopyranosyloxy]-4H-chromen-4-one 
• 849938-23-4 3,4-di-O-acetyl-2-O-benzyl-α-L-rhamnopyranosyl bromide 

Relevant articles and documents

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