2595-07-5

Basic information

• Product Name: ALLYL-BETA-D-GALACTOPYRANOSIDE
• Synonyms: ALLYL-BETA-D-GALACTOPYRANOSIDE;.beta.-D-Galactopyranoside, 2-propenyl;Allylb-galactopyranoside;allyl galactopyranoside;ALLYL-SS-D-GALACTOPYRANOSIDE;Allyl-beta-galactopyranoside;2-Propen-1-yl-beta-D-galactopyranoside;2-Propenyl-beta-D-galactoside
• CAS NO: 2595-07-5
• Molecular Formula: C₉H₁₆O₆
• Molecular Weight: 220.22
• EINECS: 1533716-785-6
• Mol File: 2595-07-5.mol
• Article Data: 67

Chemical Properties

• Boiling Point: 415 °C at 760 mmHg
• Flash Point: 204.8 °C
• Appearance: /
• Density: 1.37g/cm³
• Vapor Pressure: 1.27E-08mmHg at 25°C
• Refractive Index: 1.549
• Storage Temp.: 2-8°C
• CAS DataBase Reference: ALLYL-BETA-D-GALACTOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: ALLYL-BETA-D-GALACTOPYRANOSIDE(2595-07-5)
• EPA Substance Registry System: ALLYL-BETA-D-GALACTOPYRANOSIDE(2595-07-5)

Safety Data

• Hazardous Substances Data: 2595-07-5(Hazardous Substances Data)

Usage

Description

ALLYL-BETA-D-GALACTOPYRANOSIDE is a chemical compound that serves as a flavoring and fragrance ingredient, characterized by its galactoside structure where a galactose unit is bound to another molecule. It is naturally present in fruits and vegetables and is also synthesized for a variety of applications. ALLYL-BETA-D-GALACTOPYRANOSIDE is recognized for its sweet and fruity aroma, making it a popular choice as a flavor enhancer in the food industry and as a fragrance component in perfumes and cosmetics. Beyond its sensory attributes, ALLYL-BETA-D-GALACTOPYRANOSIDE also exhibits potential medicinal properties, such as anti-inflammatory and antioxidant effects.

Uses

Used in Food Industry:
ALLYL-BETA-D-GALACTOPYRANOSIDE is used as a flavor enhancer for its sweet and fruity aroma, adding depth and complexity to food products.
Used in Perfume and Cosmetics Industry:
ALLYL-BETA-D-GALACTOPYRANOSIDE is used as a fragrance ingredient to provide a pleasant and fruity scent in perfumes and cosmetics, enhancing the sensory experience of these products.
Used in Medicinal Applications:
ALLYL-BETA-D-GALACTOPYRANOSIDE is used for its potential anti-inflammatory and antioxidant properties, suggesting a role in the development of treatments for various conditions where these properties could be beneficial.

InChI:InChI=1/C9H16O6/c1-2-3-14-9-8(13)7(12)6(11)5(4-10)15-9/h2,5-13H,1,3-4H2/t5-,6+,7+,8-,9?/m1/s1

Upstream product

• 28244-97-5 phenyl-1-thio-α-D-galactopyranoside 
• 107-18-6 allyl alcohol 
• 28512-68-7 phenyl 2,3,4,6-tetra-O-acetyl-1-thio-α-D-galactopyranoside 
• 25878-60-8 D-galactose pentaacetate 
• 10257-28-0 D-Galactose 
• 16754-50-0 triallyl orthoformate 
• 4163-60-4 β-D-galactose peracetate 
• 10343-15-4 allyl 2,3,4,6-tetra-O-acetyl-D-galactopyranoside 
• 106-95-6 allyl bromide 
• 70191-05-8 2,3,4,6-tetra-O-acetyl-β-D-galactopyranose 
• 3646-73-9 α-D-galactopyranose 
• 7226-48-4 1,2,3,4,6-penta-O-acetyl-β-D-galactopyranoside 
• 151168-59-1 1-propynyl-β-D-galactopyranoside 
• 1190202-85-7 but-2-yn-1-yl β-D-galactopyranoside 

Downstream Products

• 99541-24-9 O-(2,3-di-O-benzyl-β-D-glucopyranosyl)-(1->4)-3-O-acetyl-1,6-anhydro-2-azido-2-deoxy-β-D-glucopyranose 
• 99541-26-1 O-(methyl 2,3-di-O-benzyl-β-D-glucopyranosyluronate)-(1->4)-3-O-acetyl-1,6-anhydro-2-azido-2-deoxy-β-D-glucopyranose 
• 1354826-74-6 (2S,3S,4R,5R,6S)-2-allyl-6-(azidomethyl)-1-benzyl-3,4,5-tris(benzyloxy)piperidine 

Relevant articles and documents

Anomeric alkylations and acylations of unprotected mono- and disaccharides mediated by pyridoneimine in aqueous solutions

A site-specific deprotonation followed by alkylations and acylations of sugar hemiacetals to the corresponding alkyl glycosides and acylated sugars in aqueous solutions is disclosed herein. Pyridoneimine as a new base is developed to mediate the deprotonation of readily available sugar hemiacetals and further reactions with alkylation and acylation agents.

Synthesis, Conformational Analysis, and Complexation Study of an Iminosugar-Aza-Crown, a Sweet Chiral Cyclam Analog

A new family of chiral C2 symmetric tetraazamacrocycles, coined ISAC for IminoSugar Aza-Crown, incorporating two iminosugars adopting a 4C1 conformation is disclosed. Multinuclear NMR experiments on the corresponding Cdsu

Preparation method of fondaparinux sodium disaccharide intermediate

The invention discloses a preparation method of fondaparinux sodium disaccharide intermediate. 1-O-substituent sulfonyl-2,3-bis-O-benzyl-4,6-O-benzylidene-beta-D-glucopyranose directly reacts with 1,6-dehydrated-2-deoxy-2-azido-3-O-acetyl-beta-D-glucopyranose to prepare the fondaparinux sodium disaccharide intermediate as shown in a formula I; and meanwhile, the fondaparinux sodium intermediate asshown in the formula I can be used as a raw material to synthesize fondaparinux sodium intermediate as shown in a formula IV. The preparation method is simple and small in steps, the yield is high, the atomic utilization rate is high, the three wastes are small, and the preparation method is suitable for industrial large-scale production. Please see the description for the formula.