150412-80-9

Basic information

• Product Name: 4-Methoxyphenyl 4-O-(beta-D-Galactopyranosyl)-beta-D-glucopyranoside
• Synonyms: 4-Methoxyphenyl 4-O-(beta-D-Galactopyranosyl)-beta-D-glucopyranoside;4-Methoxyphenyl 4-O-(b-D-galactopyranosyl)-b-D-glucopyranoside;4-Methoxyphenyl 4-O-(beta-D-Galactopyranosyl)-beta-D-glucopyranoside LacMP;4-Methoxyphenyl 4-O-β-D-Galactopyranosyl-β-D-glucopyranoside;(1-4)Glc-βGalβGalβ(1-4)Glc-&beta
• CAS NO: 150412-80-9
• Molecular Formula: C₁₉H₂₈O₁₂
• Molecular Weight: 448.42
• Mol File: 150412-80-9.mol

Chemical Properties

• Boiling Point: 742.152°C at 760 mmHg
• Flash Point: 402.639°C
• Appearance: /
• Density: 1.585g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.641
• PKA: 12.60±0.70(Predicted)
• CAS DataBase Reference: 4-Methoxyphenyl 4-O-(beta-D-Galactopyranosyl)-beta-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Methoxyphenyl 4-O-(beta-D-Galactopyranosyl)-beta-D-glucopyranoside(150412-80-9)
• EPA Substance Registry System: 4-Methoxyphenyl 4-O-(beta-D-Galactopyranosyl)-beta-D-glucopyranoside(150412-80-9)

Safety Data

• Hazardous Substances Data: 150412-80-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
4-Methoxyphenyl 4-O-(beta-D-Galactopyranosyl)-beta-D-glucopyranoside is used as a potential candidate for drug development due to its antioxidant and anti-inflammatory properties. Its presence in plant-based foods suggests that it may have beneficial effects on human health, making it a valuable compound for further research and development in the creation of new pharmaceuticals and treatments.
Used in Nutraceutical Applications:
In the nutraceutical industry, 4-Methoxyphenyl 4-O-(beta-D-Galactopyranosyl)-beta-D-glucopyranoside is used for its potential health benefits. Its antioxidant and anti-inflammatory properties may contribute to the development of dietary supplements and functional foods that promote overall health and well-being.
Used in Research and Development:
4-Methoxyphenyl 4-O-(beta-D-Galactopyranosyl)-beta-D-glucopyranoside is utilized in research and development settings to study its chemical properties, potential health benefits, and possible applications in various industries. This glycoside serves as a subject of interest for scientists and researchers who aim to understand its full potential and explore its use in creating innovative products and treatments.

InChI:InChI=1/C19H28O12/c1-27-8-2-4-9(5-3-8)28-18-16(26)14(24)17(11(7-21)30-18)31-19-15(25)13(23)12(22)10(6-20)29-19/h2-5,10-26H,6-7H2,1H3/t10-,11-,12-,13-,14+,15-,16-,17+,18+,19-/m0/s1

Upstream product

• 150-76-5 4-methoxy-phenol 
• 3616-19-1 1',2',3',6',2,3,4,6-octa-O-acetyl-β-D-lactose 
• 160227-12-3 4-methoxyphenyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-glucopyranoside 

Downstream Products

• 409060-31-7 p-methoxyphenyl (2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 717132-42-8 4-methoxyphenyl 3,4-O-isopropylidene-β-D-galactopyranosyl(1->4)-β-D-glucopyranoside 
• 1399293-58-3 4-methoxyphenyl 3'-O-[3,5-bis(trifluoromethyl)benzenesulfonyl]-β-D-lactopyranoside 
• 389812-57-1 p-methoxyphenyl O-(3-O-allyl-2-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 717132-48-4 4-methoxyphenyl 2,4,6-tri-O-benzyl-3-O-(2-naphthyl)methyl-β-D-galactopyranosyl(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 717132-51-9 4-methoxyphenyl 2,4,6-tri-O-benzyl-3-C-ethoxysulfonylmethyl-β-D-gulopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 717132-45-1 4-methoxyphenyl 2,6-di-O-benzyl-3-O-(2-naphthyl)methyl-β-D-galactopyranosyl(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 717132-47-3 4-methoxyphenyl 3-O-allyl-2,4,6-tri-O-benzyl-β-D-galactopyranosyl(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 717132-50-8 4-methoxyphenyl 2,4,6-tri-O-benzyl-β-D-xylo-hex-3-ulopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 717132-49-5 4-methoxyphenyl 2,4,6-tri-O-benzyl-β-D-galactopyranosyl(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 717132-44-0 4-methoxyphenyl 3-O-allyl-2,6-di-O-benzyl-β-D-galactopyranosyl(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 717132-43-9 4-methoxyphenyl 2,6-di-O-benzyl-3,4-O-isopropylidene-β-D-galactopyranosyl(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 358681-61-5 p-methoxyphenyl (2,6-di-O-benzyl-β-D-galactopyranosyl)-(1→4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 898826-58-9 p-methoxyphenyl 2,6-di-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-benzoyl-β-D-glucopyranoside 

Relevant articles and documents

Facile synthesis of 1-thio-β-lactoside clusters scaffolded onto p-methoxyphenyl, β-D-galactopyranoside, β-D-glucopyranoside, and lactoside

The free-radical addition of 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1 →4)-2,3,6-tri-O-acetyl-1-thio-β-D-glucopyranose to the allyl ether functions of p-methoxyphenyl per-O-allyl-D-galactopyranoside, D-glucopyranoside, and lactoside provides a concise and effective route for synthesis of glycoside clusters, of use for exploring anti-metastatic activity.

'Armed-disarmed' glycosidation strategy based on glycosyl donors and acceptors carrying phosphoroamidate as a leaving group: A convergent synthesis of globotriaosylceramide

A stereocontrolled synthesis of globotriaosylceramide with three different glycosidic linkages has been accomplished by linear and convergent routes exploiting 'armed-disarmed' glycosidation methodology based on glycosyl donors and acceptors carrying tetramethylphosphoroamidate as a leaving group. In particular, the convergent strategy featuring a coupling of a galactosyl(1→4)-galactosyl donor with a glucosylceramide derivative has proven to be extremely efficient.

Cyclo-glycosylation of (1→4)-linked glycohexaoses: Synthesis of cyclolactohexaose

Cyclo-glycosylation of (2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-{(1→4)-(2,3,6-tri-O-benzyl- β-D-glucopyranosyl)-(1→4)-(2,3,6-tri-O-benzyl-α-D- galactopyranosyl)}2-(1→4)-(2,3,6-tri-O-benzyl-α/ β-glucopyranosyl fluoride and subsequent deprotection of the product gave an excellent yield of cyclo-lactohexaose.