460745-20-4

Basic information

• Product Name: Allyl 3-O-benzyl-a-L-rhamnopyranoside
• Synonyms: Allyl 3-O-benzyl-a-L-rhamnopyranoside;Allyl 3-O-benzyl-alpha-L-rhamnopyranoside;Allyl 3-O-benzyl-α-L-rhaMnopyranoside
• CAS NO: 460745-20-4
• Molecular Formula: C₁₆H₂₂O₅
• Molecular Weight: 294.34288
• Mol File: 460745-20-4.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Allyl 3-O-benzyl-a-L-rhamnopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Allyl 3-O-benzyl-a-L-rhamnopyranoside(460745-20-4)
• EPA Substance Registry System: Allyl 3-O-benzyl-a-L-rhamnopyranoside(460745-20-4)

Safety Data

• Hazardous Substances Data: 460745-20-4(Hazardous Substances Data)

Usage

Uses

Used in Organic Chemistry and Pharmaceutical Research:
Allyl 3-O-benzyl-a-L-rhamnopyranoside is utilized as a building block for the synthesis of more complex molecules, contributing to the advancement of organic chemistry and the development of novel pharmaceuticals.
Used in the Food Industry:
In the food industry, Allyl 3-O-benzyl-a-L-rhamnopyranoside is used as a natural sweetener for its sweetening properties, offering a healthier alternative to artificial sweeteners in various foods and beverages.
Used in Drug Development:
Allyl 3-O-benzyl-a-L-rhamnopyranoside's specific chemical structure makes it a promising candidate in drug development, potentially leading to the creation of new medications with antimicrobial or antioxidant properties, enhancing therapeutic options in various medical fields.

Upstream product

• 64650-81-3 allyl α-L-rhamnopyranoside 
• 100-39-0 benzyl bromide 
• 3615-41-6 L-Rhamnose 

Downstream Products

• 460745-21-5 allyl 2,4-di-O-[(2S)-2-methylbutyryl]-3-O-benzyl-α-L-rhamnopyranoside 
• 940274-20-4 allyl 2-O-acetyl-3-O-benzyl-α-L-rhamnopyranoside 
• 940274-21-5 allyl 2-O-benzoyl-3-O-benzyl-α-L-rhamnopyranoside 
• 943307-50-4 allyl 3-O-benzyl-2-O-chloroacetyl-α-L-rhamnopyranoside 
• 940274-22-6 allyl 3-O-benzyl-2-O-(p-tolylsulfonyl)-α-L-rhamnopyranoside 
• 460745-23-7 O-2,4-di-O-[(2S)-2-methylbutyryl]-3-O-benzyl-L-rhamnopyranosyl trichloroacetimidate 
• 460745-22-6 2,4-di-O-[(2S)-2-methylbutyryl]-3-O-benzyl-α-L-rhamnopyranose 

Relevant articles and documents

Efficient synthesis of building blocks for branched rhamnogalacturonan i fragments

Starting from allyl 2-O-acetyl-3-O-benzyl-α-l-rhamnopyranoside (3), allyl (2,3,4,6-tetra-O-benzoyl-β-d-galactopyranosyl)-(1→4)-2-O-acetyl- 3-O-benzyl-α-l-rhamnopyranoside (5) was synthesized under Helferich conditions. Module 5 was converted to 2,3,4,6-te

Total synthesis of woodrosin I - Part 1: Preparation of the building blocks and evaluation of the glycosylation strategy

The preparation of three building blocks required for the total synthesis of woodrosin I (1) is outlined, a complex resin glycoside bearing a macrolide ring which spans four of the five sugars of its oligosaccharide backbone. Key steps involve the enantio

Total synthesis of woodrosin I

The reliability of ring-closing metathesis, even in complex cases, is highlighted in the first total synthesis of the structurally intriguing resin glycoside woodrosin I (1). The synthesis also shows the maturity of the trichloroacetimidate method for gly