19877-13-5

Basic information

• Product Name: 1,2-O-ISOPROPYLIDENE-3-BENZYLOXY-5,6-DIDEOXY-GLUCOFURANOSE
• Synonyms: 1,2-O-ISOPROPYLIDENE-3-BENZYLOXY-5,6-DIDEOXY-GLUCOFURANOSE
• CAS NO: 19877-13-5
• Molecular Formula: C₁₆H₂₀O₄
• Molecular Weight: 276.33
• Mol File: 19877-13-5.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 354.1°Cat760mmHg
• Flash Point: 114.2°C
• Appearance: /
• Density: 1.15g/cm³
• Vapor Pressure: 7.01E-05mmHg at 25°C
• Refractive Index: 1.544
• CAS DataBase Reference: 1,2-O-ISOPROPYLIDENE-3-BENZYLOXY-5,6-DIDEOXY-GLUCOFURANOSE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-O-ISOPROPYLIDENE-3-BENZYLOXY-5,6-DIDEOXY-GLUCOFURANOSE(19877-13-5)
• EPA Substance Registry System: 1,2-O-ISOPROPYLIDENE-3-BENZYLOXY-5,6-DIDEOXY-GLUCOFURANOSE(19877-13-5)

Safety Data

• Hazardous Substances Data: 19877-13-5(Hazardous Substances Data)

Usage

Chemical compound

A substance with a specific molecular structure that is formed by a chemical reaction.

Complex molecular structure

The compound has a complex arrangement of atoms and functional groups.

Contains isopropylidene, benzyloxy, and dideoxy functional groups

These functional groups give the compound its unique properties and reactivity.

Derivative of glucopyranose

Glucopyranose is a type of sugar, and the compound is derived from it.

Used in organic chemistry synthesis

The compound is used as a building block for more complex molecules in organic chemistry.

Building block for complex molecules

The compound can be used to create more complex molecules with potential applications.

Potential applications in the pharmaceutical industry

The compound has potential uses in the development of new drugs.

Development of antiviral and antimicrobial agents

The compound may be used to create new drugs that fight viruses and bacteria.

Unique structure and reactivity

The compound's structure and reactivity make it a valuable tool for creating novel chemical compounds.

Creation of novel chemical compounds with potential therapeutic properties

The compound can be used to create new compounds that may have therapeutic benefits.

InChI:InChI=1/C16H20O4/c1-4-12-13(17-10-11-8-6-5-7-9-11)14-15(18-12)20-16(2,3)19-14/h4-9,12-15H,1,10H2,2-3H3/t12-,13+,14?,15?/m1/s1

Upstream product

• 22331-18-6 O³-benzyl-O¹,O²-isopropylidene-O⁵,O⁶-bis-(toluene-4-sulfonyl)-α-D-glucofuranose 
• 60-29-7 diethyl ether 
• 917-54-4 methyllithium 
• 35781-78-3 5,6-anhydro-3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 18439-45-7 3-O-benzyl-6-deoxy-1,2-O-isopropylidene-5-C-methyl-β-L-ido-pentofuranose 
• 99750-18-2 3-O-benzyl-6-deoxy-1,2-O-isopropylidene-5-O-methanesulfonyl-β-L-idofuranose 
• 22331-19-7 3-O-benzyl-1,2-O-isopropylidene-5,6-di-O-mesyl-α-D-glucofuranose 
• 868078-60-8 (3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-5-oxiranyl-tetrahydro-furo[2,3-d][1,3]dioxole 
• 18439-45-7 3-O-Benzyl-6-desoxy-1,2-O-isopropyliden-α-D-gluco-hexofuranose 
• 22529-61-9 (1R)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro(2,3-d)(1,3)dioxol-5-yl)ethane-1,2-diol 
• 127666-20-0 3-O-benzyl-6-deoxy-6-iodo-1,2-O-isopropylidene-5-O-(diphenylphosphinyl)-α-D-glucofuranose 
• 120368-01-6 3-O-benzyl-6-deoxy-1,2-O-isopropylidene-5-O-methanesulphonyl-α-D-glucofuranose 
• 100-39-0 benzyl bromide 
• 7284-07-3 5,6-dideoxy-1,2-O-isopropylidene-α-D-xylo-hex-5-eno-furanose 

Downstream Products

• 30361-13-8 (4S)-O³-benzyl-O¹,O²-isopropylidene-4-[(Ξ)-3-(4-nitro-phenyl)-4,5-dihydro-isoxazol-5-yl]-β-L-threofuranose 
• 149774-48-1 (5R)-5-(3-O-benzyl-1,2-O-isopropylidene-α-D-xylo-tetrofuranos-4-yl)-3-(1,2:3,4-di-O-isopropylidene-D-arabino-tetritol-1-yl)-4,5-dihydroisoxazole 
• 18417-40-8 diethyl 1,2,5-oxadiazole-3,4-dicarboxylate 2-oxide 
• 118226-62-3 (5R)-5-(3-O-benzyl-1,2-O-isopropylidene-α-D-xylo-tetrafuranos-4-yl)-3-ethoxycarbonyl-2-isoxazoline 
• 118374-38-2 (5S)-5-(3-O-benzyl-1,2-O-isopropylidene-α-D-xylo-tetrafuranos-4-yl)-3-ethoxycarbonyl-2-isoxazoline 
• 888-71-1 3,5-diphenyl-1,2,4-oxadiazole 
• 5585-14-8 3,4-diphenyl-furazan 2-oxide 
• 118332-61-9 (5R)-5-(3-O-benzyl-1,2-O-isopropylidene-α-D-xylo-tetrafuranos-4-yl)-3-phenyl-2-isoxazoline 
• 118332-63-1 (5S)-5-(3-O-benzyl-1,2-O-isopropylidene-α-D-xylo-tetrafuranos-4-yl)-3-phenyl-2-isoxazoline 
• 80502-02-9 methyl 3-O-benzyl-5,6-dideoxy-α,β-D-xylo-hex-5-enofuranoside 
• 89755-60-2 (-)-3-O-benzyl-5-deoxy-5-C-methyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 204057-85-2 (3aR,5S,6R,6aR)-6-Benzyloxy-5-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-1-iodo-decyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole 
• 204057-92-1 (3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-5-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyl)-tetrahydro-furo[2,3-d][1,3]dioxole 
• 204057-84-1 (3aR,5S,6R,6aR)-6-Benzyloxy-2,2-dimethyl-5-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-1-iodo-octyl)-tetrahydro-furo[2,3-d][1,3]dioxole 

Relevant articles and documents

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Construction of key building blocks towards the synthesis of cortistatins

This work reports the construction of key building blocks towards the synthesis of cortistatins; a family of steroidal alkaloids. Cortistatin A, being a primary target due to its superior biological properties over other congeners, has been prepared by two different synthetic routes. Synthesis of the precursor to the heavily substituted A-ring starting from d-glucose and construction of the DE-ring junction employing a Hajos-Parrish ketone as a chiral pool have been demonstrated. Efforts are underway to assemble these key fragments and build towards the total synthesis of cortistatin A.

Synthesis of a furanosyl-pyranone derivative related to the tri-o-heterocyclic core of herbicidins

A new compound that is structurally related to the undecose ring structure of herbicidins has been prepared. The synthesis of this novel furanosyl-pyranone derivative was made possible through the regioselective reductive ring-opening of a 3,5-O-benzylidene-D-xylofuranose and the hetero-Diels-Alder reaction of an aldehyde and a Danishefsky-type diene. The highly functionalized pyranone derivative can be a useful precursor for the synthesis of herbicidins.