84518-62-7 Usage
Uses
Used in Pharmaceutical Industry:
2,5-3,4-Dianhydroaltritol is used as a building block for the development of various drugs and drug intermediates due to its unique structure and reactivity, which allows for the creation of a wide range of pharmaceutical compounds.
Used in Organic Synthesis:
2,5-3,4-Dianhydroaltritol is used as a versatile compound in organic synthesis for its potential to form a variety of chemical products, given its reactivity and cyclic ether nature.
Used in Research:
2,5-3,4-Dianhydroaltritol is used as a subject of research for its potential biological activity, with further studies needed to fully understand its properties and explore additional applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 84518-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,1 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 84518-62:
(7*8)+(6*4)+(5*5)+(4*1)+(3*8)+(2*6)+(1*2)=147
147 % 10 = 7
So 84518-62-7 is a valid CAS Registry Number.
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
84518-62-7Relevant academic research and scientific papers
Efficient and Easy Access to Optically Pure Tetrasubstituted Tetrahydrofurans via Stereoselective Opening of C2-Symmetric Epoxide and Aziridine Rings
Kumar Kondapi, Venkata Pavan,Soueidan, Olivier-Mohamad,Hosseini, Seyedeh Nargess,Jabari, Nauras,West, Frederick G.
, p. 1367 - 1379 (2016/03/16)
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
Otero, Dario A.,Simpson, Ronald
, p. 79 - 86 (2007/10/02)
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.
