400091-05-6

Basic information

• Product Name: 4-METHOXYPHENYL 3-O-ALLYL-4,6-O-BENZYLIDENE-BETA-D-GALACTOPYRANOSIDE
• Synonyms: 4-METHOXYPHENYL 3-O-ALLYL-4,6-O-BENZYLIDENE-BETA-D-GALACTOPYRANOSIDE;4-Methoxyphenyl3-O-allyl-4,6-O-benzylidene-b-D-galactopyranoside;4-Methoxyphenyl 3-O-Allyl-4,6-O-benzylidene-β-D-galactopyranoside;4-Methoxyphenyl 3-O-allyl-4,6-O-benzylidene-β-D-galactopyranoside ,98%;4-Methoxyphenyl 3-O-Allyl-4,6-O-benzylidene-β(4AR,6S,7R,8R,8aS)-8-(allyloxy)-6-(4-methoxyphenoxy)-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-ol;(2S,4aR,6S,7R,8R,8aS)-6-(4-methoxyphenoxy)-2-phenyl-8-prop-2-enoxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-7-ol
• CAS NO: 400091-05-6
• Molecular Formula: C₂₃H₂₆O₇
• Molecular Weight: 414.45
• Product Categories: Biochemistry;Galactose;Glycosides;O-Substituted Sugars;Sugars
• Mol File: 400091-05-6.mol
• Article Data: 2

Chemical Properties

• Melting Point: 228 °C
• Boiling Point: 589.86oC at 760 mmHg
• Flash Point: 310.536oC
• Appearance: /
• Density: 1.278g/cm3
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: -47.5 ° (C=0.5, Pyridine)
• Storage Temp.: Freezer
• PKA: 12.58±0.70(Predicted)
• CAS DataBase Reference: 4-METHOXYPHENYL 3-O-ALLYL-4,6-O-BENZYLIDENE-BETA-D-GALACTOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHOXYPHENYL 3-O-ALLYL-4,6-O-BENZYLIDENE-BETA-D-GALACTOPYRANOSIDE(400091-05-6)
• EPA Substance Registry System: 4-METHOXYPHENYL 3-O-ALLYL-4,6-O-BENZYLIDENE-BETA-D-GALACTOPYRANOSIDE(400091-05-6)

Safety Data

• Hazardous Substances Data: 400091-05-6(Hazardous Substances Data)

Usage

Chemical Properties

White solid

InChI:InChI=1/C23H26O7/c1-3-13-26-21-19(24)23(28-17-11-9-16(25-2)10-12-17)29-18-14-27-22(30-20(18)21)15-7-5-4-6-8-15/h3-12,18-24H,1,13-14H2,2H3/t18-,19-,20+,21-,22+,23-/m1/s1

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 144985-19-3 p-methoxyphenyl 3-O-allyl-β-D-galactopyranoside 
• 3150-20-7 4-methoxyphenyl β-D-galactopyranoside 
• 150-76-5 4-methoxy-phenol 
• 4163-60-4 β-D-galactose peracetate 
• 2872-65-3 4-methoxyphenyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 

Downstream Products

• 400091-16-9 phenyl 3-O-allyl-6-O-benzyl-2-O-pivaloyl-1-thio-β-D-galactopyranoside 
• 400091-07-8 4-methoxyphenyl 3-O-allyl-6-O-benzyl-2-O-pivaloyl-β-D-galactopyranoside 
• 400091-21-6 phenyl 4-O-acetyl-3-O-allyl-6-O-benzyl-2-O-pivaloyl-1-thio-β-D-galactopyranoside 
• 144985-21-7 Acetic acid (2R,3R,4S,5S,6R)-4-allyloxy-5-benzyloxy-6-benzyloxymethyl-2-chloro-tetrahydro-pyran-3-yl ester 
• 144985-28-4 Acetic acid (4aR,6S,7R,8S,8aS)-8-allyloxy-6-[(2R,3S,4S,5R,6S)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-((3R,4S,5R,6R)-4,5,6-tris-benzyloxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 
• 144985-29-5 (4aR,6S,7R,8S,8aR)-7-Benzyloxy-6-[(2R,3S,4S,5R,6S)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-((3R,4S,5R,6R)-4,5,6-tris-benzyloxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-ol 
• 144985-26-2 2,2-Dimethyl-propionic acid (2R,3R,4S,5R)-5-((2S,3R,4S,5S,6R)-3-acetoxy-4-allyloxy-5-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-2,4-bis-benzyloxy-tetrahydro-pyran-3-yl ester 
• 144985-35-3 2,2-Dimethyl-propionic acid (2R,3R,4S,5R)-5-((2R,3R,4S,5S,6R)-3-acetoxy-4-allyloxy-5-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-2,4-bis-benzyloxy-tetrahydro-pyran-3-yl ester 
• 144985-27-3 2,2-Dimethyl-propionic acid (2R,3R,4S,5R)-5-((2S,3R,4S,5S,6R)-4-allyloxy-3,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-2,4-bis-benzyloxy-tetrahydro-pyran-3-yl ester 
• 144985-16-0 2,2-Dimethyl-propionic acid (2R,3R,4S,5R)-2,4-bis-benzyloxy-5-((2S,3R,4S,5R,6R)-3,5-bis-benzyloxy-6-benzyloxymethyl-4-hydroxy-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl ester 
• 144985-20-6 Acetic acid (2S,3R,4S,5S,6R)-4-allyloxy-6-benzyloxymethyl-5-hydroxy-2-(4-methoxy-phenoxy)-tetrahydro-pyran-3-yl ester 
• 400091-06-7 4-methoxyphenyl 3-O-allyl-4,6-O-benzylidene-2-O-pivaloyl-β-D-galactopyranoside 

Relevant articles and documents

Directed and efficient syntheses of β(1→4)-linked galacto-oligosaccharides

Straightforward, preparatively efficient procedures are described for the construction of β(1→4)-intergalactosidic linkages up to the hexasaccharide level. Key elements were the use of phenylthio and/or phenyl sulfoxide functionalities for glycosylations and a judiciously designed blocking group pattern for donor and acceptor alike: pivaloyl protection at O-2 for securing β-selectivity, sterically undemanding allyl or benzyl groups at O-3 and O-6 to minimise the steric bulk around the unreactive galactosyl-4-OH, the p-methoxyphenyl moiety, readily replaceable by SPh, as an intermediate anomeric substituent, and an acetyl group for temporary protection of the terminal Gal-4-OH. This strategy lends itself to iterative block synthesis and interchange of donors and acceptors, thereby demonstrating the broad scope and generality of the overall approach. Although predicted by molecular modelling, inclinations towards starch-like coiling could not so far be verified in any of the galacto-tetra-, -penta-, or -hexaoses or their p-methoxyphenyl glycosides.