159407-19-9

Basic information

• Product Name: Phenyl 4,6-O-Benzylidene-1-thio-a-D-mannopyranoside
• Synonyms: Phenyl 4,6-O-[(R)-Phenylmethylene]-1-thio-α-D-mannopyranoside;Phenyl 4,6-O-Benzylidene-1-thio-α-D-mannopyranoside; Phenyl 4,6-O-(Phenylmethylene)-1-thio-a-D-mannopyranoside;Phenyl 4,6-O-[(R)-Phenylmethylene]-1-thio-a-D-mannopyranoside;Phenyl 4,6-O-Benzylidene-1-thio-a-D-mannopyranoside;Phenyl 4,6-O-(Phenylmethylene)-1-thio-α-D-mannopyranoside
• CAS NO: 159407-19-9
• Molecular Formula: C₁₉H₂₀O₅S
• Molecular Weight: 360.42
• Product Categories: Aromatics Compounds;Aromatics;Carbohydrates & Derivatives;Sulfur & Selenium Compounds
• Mol File: 159407-19-9.mol
• Article Data: 26

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• Solubility: Chloroform
• CAS DataBase Reference: Phenyl 4,6-O-Benzylidene-1-thio-a-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Phenyl 4,6-O-Benzylidene-1-thio-a-D-mannopyranoside(159407-19-9)
• EPA Substance Registry System: Phenyl 4,6-O-Benzylidene-1-thio-a-D-mannopyranoside(159407-19-9)

Safety Data

• Hazardous Substances Data: 159407-19-9(Hazardous Substances Data)

Usage

Description

Phenyl 4,6-O-Benzylidene-1-thio-α-D-mannopyranoside, with the CAS number 159407-19-9, is a white solid compound that is primarily utilized in the field of organic synthesis. It is a derivative of mannopyranoside, which is a type of sugar molecule, and features a benzylidene group attached to the 4,6-O positions. This unique structure makes it a valuable component in the synthesis of various organic compounds.

Uses

Used in Organic Synthesis:
Phenyl 4,6-O-Benzylidene-1-thio-α-D-mannopyranoside is used as a synthetic building block for the creation of complex organic molecules. Its unique structure allows for a wide range of applications in the synthesis of various compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Phenyl 4,6-O-Benzylidene-1-thio-α-D-mannopyranoside is used as a key intermediate in the synthesis of novel drug candidates. Its unique structure can be exploited to design and develop new molecules with potential therapeutic applications.
Used in Research and Development:
Phenyl 4,6-O-Benzylidene-1-thio-α-D-mannopyranoside is also used in research and development laboratories for the study of various chemical reactions and processes. Its unique structure makes it an ideal candidate for exploring new synthetic routes and methodologies in organic chemistry.
Used in Material Science:
In the field of material science, Phenyl 4,6-O-Benzylidene-1-thio-α-D-mannopyranoside can be used as a component in the development of new materials with specific properties. Its unique structure can contribute to the design of materials with tailored characteristics, such as improved stability, reactivity, or selectivity.

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 2936-70-1 (2R,3S,4S,5S,6R)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol 
• 65236-83-1 phenyl 2,3,4,6-tetra-O-benzoyl-1-thio-α-D-mannopyranoside 
• 83-87-4 D-Mannose pentaacetate 
• 13992-16-0 phenyl 2,3,4,6-tetra-O-acetyl-1-thio-α-D-mannopyranoside 
• 108-98-5 thiophenol 
• 4163-65-9 per-O-acetyl-α-D-mannopyranose 
• 530-26-7 D-Mannose 
• 121524-01-4 phenyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-mannopyranoside 
• 151763-69-8 phenyl 1-thio-D-mannopyranoside 

Downstream Products

• 159407-17-7 phenyl 2,3-di-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside 
• 158716-07-5 phenyl 3-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside 
• 168138-26-9 phenyl 4,6-O-benzylidene-3-O-(4-methoxybenzyl)-1-thio-α-D-mannopyranoside 
• 263543-67-5 S-phenyl 2,3-O-carbonyl-4,6-O-benzylidene-1-thia-α-D-mannopyranoside 
• 407616-82-4 S-phenyl 2,3-di-O-allyl-4,6-O-benzylidene-1-thia-α-D-mannopyranoside 
• 407616-83-5 S-phenyl 2,3-di-O-p-bromobenzyl-4,6-O-benzylidene-1-thia-α-D-mannopyranoside 
• 403646-50-4 S-phenyl 4,6-O-benzylidene-2,3-di-O-(p-methoxybenzyl)-1-thio-α-D-mannnopyranoside 
• 158716-08-6 phenyl 4,6-O-benzylidene-2-O-benzyl-1-deoxy-1-thio-α-D-mannopyranoside 
• 634597-88-9 (2R,4aR,6R,7S,8R,8aR)-8-(tert-Butyl-diphenyl-silanyloxy)-2-phenyl-6-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol 
• 340161-12-8 phenyl 2-O-acetyl-4,6-O-banelidene-1-thio-α-D-mannopyranoside 
• 915221-33-9 phenyl 4,6-O-benzylidene-3-O-(3-naphthalen-1-yl-prop-2-ynyl)-1-thio-α-D-mannopyranoside 
• 922183-00-4 phenyl 4,6-O-benzylidene-3-O-tert-butyldimethylsilyl-1-thio-α-D-mannopyranoside 
• 951025-06-2 phenyl 4,6-O-benzylidene-3-O-(2-methylnaphthyl)-1-thio-α-D-mannopyranoside 
• 855306-46-6 methyl 4,6-O-benzylidene-2-O-(prop-2-ynyl)-β-D-mannopyranoside 

Relevant articles and documents

Synthesis of optically pure, differentially protected 1,4- and 1,6-mannosyl-D-myo-inositol derivatives from 7-oxabicyclo[2.2.1]heptan-2-one

Efficient procedures to prepare 4-O-mannosyl conduritol B derivatives from mannosyl oxanorbornanes are described. The osmium-catalyzed cis-dihydroxylation of the corresponding 1-O-acetates displays high π-facial selectivity syn to the acetate functionalit

Deuterium labelling to extract local stereochemical information by VCD spectroscopy in the C-D stretching region: A case study of sugars

Stereochemical elucidation of molecules with multiple chiral centers is difficult. Even with VCD spectroscopy, excluding all but one diastereomeric structural candidate is challenging because the stereochemical inversion of one chiral center among many centers does not always result in noticeable differences in their VCD spectra. This work demonstrates that the introduction of a suitable VCD chromophore with absorption in the 2300-1900 cm-1 region can be used for extracting local stereochemical information and for the stereochemical assignment of the C-1 position of various sugars as a case study. Through studies on a series of epimeric pairs of monosaccharides and their derivatives, we found that the introduction of one -OCD3 group to each C-1 position produced almost mirror-image VCD patterns in the 2300-1900 cm-1 region depending on the C-1 stereochemistry irrespective of the other molecular moieties. This work also shows that comparison of the observed VCD signals and the calculated ones enables the stereochemical assignment of a chiral center in the vicinity of the chromophore. This study provides a proof of concept that the use of a VCD chromophore in the 2300-1900 cm-1 region enables the analysis of selected stereochemistry of suitable molecular systems. Further studies on this concept should lead to the development of a method useful for the structural elucidation of other types of complex molecules.

A Synthetic Carbohydrate-Protein Conjugate Vaccine Candidate against Klebsiella pneumoniae Serotype K2

Klebsiella pneumoniae causes pneumonia and liver abscesses in humans worldwide and contains virulence factor capsular polysaccharides and lipopolysaccharides linked to the cell wall. Although capsular polysaccharides are good antigens for vaccine producti