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
• Article Data: 3

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

General Description

Allyl 3-O-benzyl-a-L-rhamnopyranoside is a chemical compound that consists of an allyl group attached to the third carbon of a benzyl group which is in turn attached to a-L-rhamnopyranose. Allyl 3-O-benzyl-a-L-rhamnopyranoside is a type of glycoside, which is a molecule that contains a sugar group bonded to a non-sugar group. It is often used in organic chemistry and pharmaceutical research as a building block for the synthesis of more complex molecules. Additionally, it has potential applications in the food industry, as glycosides are known for their sweetening properties and may be used as natural sweeteners in foods and beverages. The compound's specific chemical structure makes it useful in the development of new drugs and may also have antimicrobial or antioxidant properties.

Upstream product

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

Downstream Products

• 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 
• 460745-21-5 allyl 2,4-di-O-[(2S)-2-methylbutyryl]-3-O-benzyl-α-L-rhamnopyranoside 

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

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