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

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

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

Synthesis of a potent and selective inhibitor of p90 Rsk

(Chemical Equation Presented) The synthesis of the naturally occurring kaempferol glycoside SL0101 has been accomplished, as has its biochemical evaluation. SL0101 exhibits selective and potent p90 Rsk inhibitory activity at nanomolar concentrations without inhibiting the function of upstream kinases such as MEK, Raf, or PKC. The synthesis verified the structural assignment of the natural product and has provided access to material sufficient for detailed biological evaluation.