488-64-2

Basic information

• Product Name: inosose
• Synonyms: inosose;(2S)-2β,3α,4β,5α,6β-Pentahydroxycyclohexanone;1-Oxo-1-deoxy-L-scyllo-inositol;2-Oxo-2-deoxy-myo-inositol;D-myo-2-Inosose;myo-2-Inosose;myo-Inosose- 2;D-epi-3-Inosose
• CAS NO: 488-64-2
• Molecular Formula: C₆H₁₀O₆
• Molecular Weight: 178.14
• Mol File: 488-64-2.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 368.6°Cat760mmHg
• Flash Point: 190.9°C
• Appearance: /
• Density: 2.026g/cm³
• Vapor Pressure: 6.25E-07mmHg at 25°C
• Refractive Index: 1.748
• CAS DataBase Reference: inosose(CAS DataBase Reference)
• NIST Chemistry Reference: inosose(488-64-2)
• EPA Substance Registry System: inosose(488-64-2)

Safety Data

• Hazardous Substances Data: 488-64-2(Hazardous Substances Data)

Usage

Description

Inosose is a carbohydrate derivative belonging to the class of inositol glycosides. It is a cyclic sugar derivative that can be found in trace amounts in certain plants and microorganisms. Due to its unique chemical structure and properties, inosose has potential pharmaceutical and biotechnological applications.

Uses

Used in Pharmaceutical Formulations:
Inosose is used as a drug carrier or stabilizer for enhancing the efficacy and stability of pharmaceutical formulations.
Used in Production of Natural Products and Biofuels:
Inosose serves as a key component in the production of natural products and biofuels, contributing to the development of sustainable energy sources and eco-friendly products.
Used in Therapeutic Applications:
Inosose is used as a potential therapeutic agent for the treatment of various diseases, including cancer and neurodegenerative disorders, due to its promising medicinal properties.
Used in Research and Development:
Inosose is utilized in research and development for further exploration of its potential applications and to unlock new possibilities in the fields of medicine, biotechnology, and energy.

InChI:InChI=1/C6H10O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-5,7-11H/t1?,2-,3+,4+,5-

Upstream product

• 106600-11-7 2,3,4,5,6-penta-O-benzyl-scyllo-inosose 
• 319-89-1 tetrahydroxy-1,4-quinone 
• 87-89-8 D-myo-inositol 
• 576-63-6 cis-inositol 

Downstream Products

• 15110-70-0 Croconic acid dianion 
• 28737-41-9 Rhodizonate dianion 
• 527-42-4 1-deoxy-scyllo-inositol 
• 7045-48-9 myo-inosose-⁽²⁾-phenylhydrazone 
• 1254-38-2 inositol peracetate 
• 20108-71-8 hexa-O-acetyl-epi-inositol 
• 87-89-8 D-myo-inositol 
• 488-58-4 epi-Inositol 
• 69422-80-6 ubiquinol-3 
• 95778-33-9 1,2,3,4-tetramethoxy-5-methyl-6-((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)benzene 
• 35896-58-3 2,3,4,5-tetramethoxytoluene 
• 21450-56-6 1,2,3,4-tetramethoxybenzene 
• 642-96-6 1,2,3,4-tetrahydroxybenzene 
• 24924-09-2 1,2,3,5-tetraacetoxy-benzene 

Relevant articles and documents

Protecting group directed stereoselective reduction of an epi-inosose: Efficient synthesis of epi-inositol

A facile and high yielding synthesis of epi-inositol via stereoselective reduction of a pentaprotected epi-inosose is reported. Extent of stereoselectivity during the hydride reduction appears to depend on the ability of the substrate to complex with metal ions in the reducing agent.

Stereoselective oxidation of protected inositol derivatives catalyzed by inositol dehydrogenase from Bacillus subtilis

Inositol dehydrogenase (EC 1.1.1.18) from Bacillus subtilis is shown to have a nonpolar cavity adjacent to the active site, allowing racemic protected inositol derivatives such as 4-O-benzyl-myo-inositol to be recognized with very high apparent stereoselectivity.

Synthesis of 1,2,3,4-tetrahydroxybenzene from D-glucose: Exploiting myo- inositol as a precursor to aromatic chemicals [11]

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