1352561-81-9

Basic information

• Product Name: C₂₈H₃₀O₆S
• Synonyms: C₂₈H₃₀O₆S
• CAS NO: 1352561-81-9
• Molecular Weight: 494.609
• Mol File: 1352561-81-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₂₈H₃₀O₆S(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₈H₃₀O₆S(1352561-81-9)
• EPA Substance Registry System: C₂₈H₃₀O₆S(1352561-81-9)

Safety Data

• Hazardous Substances Data: 1352561-81-9(Hazardous Substances Data)

Usage

General Description

C28H30O6S is a chemical compound that is classified as an organic sulfur compound. It consists of 28 carbon atoms, 30 hydrogen atoms, 6 oxygen atoms, and 1 sulfur atom, and has a molecular weight of 490.6 g/mol. C₂₈H₃₀O₆S's structure indicates the presence of several functional groups, including carbon-carbon double bonds, carbon-carbon single bonds, and sulfur-hydrogen bonds. The specific properties and uses of this compound are not specified in the chemical formula alone, so further information about its intended application, potential hazards, and reactivity would be needed to fully understand its significance.

Upstream product

• 604-69-3 β-D-glucose pentaacetate 
• 67-56-1 methanol 
• 868241-49-0 (p-methylphenyl) 4,6-O-benzylidene-1-thio-β-D-glucopyranoside 
• 1152-39-2 p-methylphenyl 1-thio-β-D-glucopyranoside 
• 106-45-6 para-thiocresol 
• 28244-94-2 p-tolyl-2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 850416-39-6 p-methylphenyl 2,3-di-O-benzyl-4,6-O-(R)-benzylidene-1-thio-β-D-glucopyranoside 
• 219518-19-1 4-methylphenyl 4,6-O-benzylidene-1-thio-β-D-glucopyranoside 
• 74-88-4 methyl iodide 
• 596087-18-2 4-methylphenyl 2,3-di-O-benzyl-1-thio-β-D-glucopyranoside 

Downstream Products

• 1352561-84-2 C₅₁H₅₆O₁₃ 
• 1352561-50-2 C₃₀H₃₂O₇S 
• 87907-01-5 methyl (2,3-di-O-benzyl-4-O-chloroacetyl-α-D-glucopyranosyl bromide)uronate 
• 87907-02-6 O-(methyl 2,3-di-O-benzyl-4-O-(chloroacetyl)-β-D-glucopyranosyluronate)-(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 
• 99541-27-2 O-(6-O-acetyl-2-azido-3,4-di-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-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 
• 135362-96-8 O-(6-O-acetyl-2-azide-3,4-di-O-benzyl-2-deoxy-2-α-D-glucopyranosyl)-(1→4)-O-(methyl 2,3-di-O-benzyl-β-D-glucopyranosyluronate)-(1→4)-3,6-di-O-acetyl-2-azido-2-deoxy-β-D-glucopyranosyl trichloroacetimidate 
• 135362-95-7 O-(6-O-acetyl-2-azide-3,4-di-O-benzyl-2-deoxy-2-α-D-glucopyranosyl)-(1→4)-O-(methyl 2,3-di-O-benzyl-β-D-glucopyranosyluronate)-(1→4)-3,6-di-O-acetyl-2-azido-2-deoxy-α-D-glucopyranosyl trichloroacetimidate 
• 1610791-09-7 C₃₀H₃₁ClO₇S 

Relevant articles and documents

PREPARATION OF MONOSACCHARIDES, DISACCHARIDES, TRISACCHARIDES, AND PENTASACCHARIDES OF HEPARINOIDS

The present invention provides preparations of monosaccharides, disaccharides, trisaccharides, and pentasaccharides of heparinoids. The present invention also provides novel monosaccharides, disaccharides, trisaccharides and pentasaccharides for use in th

Exploring and exploiting the reactivity of glucuronic acid donors

The relative reactivity of glucuronic acid esters was established in a series of competition experiments, in which two thioglucoside and/or thioglucuronic acid ester donors competed for a limited amount of activator (NIS-TfOH). Although glucuronic acid esters are often considered to be of very low reactivity, the series of competition reactions revealed that the reactivity of the glucuronic acid esters studied is sufficient to provide productive glycosylation reactions. The latter is illustrated in the synthesis of two Streptococcus pneumoniae trisaccharides, in which the applicability of the two similarly protected frame-shifted thiodisaccharide donors, Glc-GlcA and GlcA-Glc, were compared. The Glc-GlcA disaccharide, featuring the glucuronic acid donor moiety, proved to be the most productive in the assembly of a protected S. pneumoniae trisaccharide.