84709-85-3 Usage
Description
(3S,4S)-TETRAHYDROFURAN-3,4-DIOL is a tetrahydrofuran derivative, a type of organic compound characterized by a five-membered ring structure containing two oxygen atoms. It is a chiral molecule with specific stereochemistry, having the 3S and 4S configurations, which makes it a unique and valuable compound for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
(3S,4S)-TETRAHYDROFURAN-3,4-DIOL is used as a chiral building block for the synthesis of pharmaceutical compounds. Its unique stereochemistry allows for the creation of enantiomerically pure drugs, which can have different biological activities and reduce potential side effects.
Used in Chemical Synthesis:
(3S,4S)-TETRAHYDROFURAN-3,4-DIOL is used as an intermediate in the synthesis of various organic compounds, including natural products, agrochemicals, and other specialty chemicals. Its versatile structure and functional groups make it a valuable component in the development of new molecules with potential applications.
Used in Material Science:
(3S,4S)-TETRAHYDROFURAN-3,4-DIOL is used in the preparation of hyperbranched carbohydrate polymers via ring-opening reaction. These polymers have potential applications in various fields, such as drug delivery, tissue engineering, and nanotechnology, due to their unique properties, such as high molecular weight, branched structure, and biocompatibility.
Used in Research and Development:
(3S,4S)-TETRAHYDROFURAN-3,4-DIOL is used as a labelled analogue of 1,4-Anhydro-L-threitol, another tetrahydrofuran derivative. This allows researchers to study the properties and behavior of these compounds in various chemical and biological systems, leading to a better understanding of their potential applications and limitations.
Check Digit Verification of cas no
The CAS Registry Mumber 84709-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,0 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84709-85:
(7*8)+(6*4)+(5*7)+(4*0)+(3*9)+(2*8)+(1*5)=163
163 % 10 = 3
So 84709-85-3 is a valid CAS Registry Number.
84709-85-3Relevant articles and documents
Intramolecular dehydration of biomass-derived sugar alcohols in high-temperature water
Yamaguchi, Aritomo,Muramatsu, Natsumi,Mimura, Naoki,Shirai, Masayuki,Sato, Osamu
, p. 2714 - 2722 (2017)
The intramolecular dehydration of biomass-derived sugar alcohols d-sorbitol, d-mannitol, galactitol, xylitol, ribitol, l-arabitol, erythritol, l-threitol, and dl-threitol was investigated in high-temperature water at 523-573 K without the addition of any acid catalysts. d-Sorbitol and d-mannitol were dehydrated into isosorbide and isomannide, respectively, as dianhydrohexitol products. Galactitol was dehydrated into anhydrogalactitols; however, the anhydrogalactitols could not be dehydrated into dianhydrogalactitol products because of the orientation of the hydroxyl groups at the C-3 and C-6 positions. Pentitols such as xylitol, ribitol, and l-arabitol were dehydrated into anhydropentitols. The dehydration rates of the pentitols containing hydroxyl groups in the trans form, which remained as hydroxyl groups in the product tetrahydrofuran, were larger than those containing hydroxyl groups in the cis form because of the structural hindrance caused by the hydroxyl groups in the cis form during the dehydration process. In the case of the tetritols, the dehydration of erythritol was slower than that of threitol, which could also be explained by the structural hindrance of the hydroxyl groups. The dehydration of l-threitol was faster than that of dl-threitol, which implies that molecular clusters were formed by hydrogen bonding between the sugar alcohols in water, which could be an important factor that affects the dehydration process.
