84518-62-7

Basic information

• Product Name: 2,5-3,4-dianhydroaltritol
• Synonyms: 2,5-3,4-dianhydroaltritol;2,5:3,4-dianhydro-D-Altritol
• CAS NO: 84518-62-7
• Molecular Formula: C₆H₁₀O₄
• Molecular Weight: 146.141
• Mol File: 84518-62-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 310.2°C at 760 mmHg
• Flash Point: 141.4°C
• Appearance: /
• Density: 1.369g/cm³
• Vapor Pressure: 5.46E-05mmHg at 25°C
• Refractive Index: 1.514
• CAS DataBase Reference: 2,5-3,4-dianhydroaltritol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-3,4-dianhydroaltritol(84518-62-7)
• EPA Substance Registry System: 2,5-3,4-dianhydroaltritol(84518-62-7)

Safety Data

• Hazardous Substances Data: 84518-62-7(Hazardous Substances Data)

Usage

General Description

2,5-3,4-dianhydroaltritol is a chemical compound that belongs to the class of alcohols. It is a cyclic ether and has a molecular formula C6H10O3. It is synthesized from sugar alcohols and has potential applications in the pharmaceutical industry as a building block for various drugs and drug intermediates. Its unique structure and reactivity make it a versatile compound for use in organic synthesis, and it is of interest to researchers for its potential biological activity. However, further studies are needed to fully understand its properties and potential uses.

InChI:InChI=1/C6H10O4/c7-1-3-5-6(10-5)4(2-8)9-3/h3-8H,1-2H2/t3-,4-,5-,6+/m1/s1

Upstream product

• 66-84-2 D-(+)-glucosamine hydrochloride 
• 41107-82-8 2,5-anhydro-D-mannitol 
• 128899-62-7 (2R,2'R,3'S,2''S)-[2,2';3',2'']Teroxirane 

Downstream Products

• 798574-25-1 2,5:3,4-dianhydro-1,6-di-O-trityl-D-altritol 
• 91383-05-0 2,5-anhydro-1,6-di-O-benzoyl-D-iditol 
• 91318-12-6 2,5:3,4-dianhydro-1,6-di-O-benzoyl-D-altritol 

Relevant articles and documents

Efficient and Easy Access to Optically Pure Tetrasubstituted Tetrahydrofurans via Stereoselective Opening of C2-Symmetric Epoxide and Aziridine Rings

An efficient and facile protocol to functionalize position C-3 of 2,5-anhydro-D-mannitol via diastereoselective ring opening of a C2-symmetric epoxide 2,5:3,4-dianhydro-D-allitol 3 has been developed. This method is protecting-group-free, high-

2,5-ANHYDRO-D-HEXITOLS: SYNTHESES OF 2,5-ANHYDRO-D-ALTRITOL AND 2,5-ANHYDRO-D-IDITOL

2,5-Anhydro-D-altritol (2a) and the previously-unknown 2,5-anhydro-D-iditol (3a) have been prepared from 2,5-anhydro-D-mannitol (1a).The preparation of 3a from the intermediate epoxide 7b is particularly sensitive to pH, and a mechanism is proposed to explain this.Attention is drawn to the limitations of the trifluoroperacetic acid-disodium hydrogenphosphate procedure for the epoxidation of alkenes of diminished reactivity.