164267-53-2 Usage
Uses
Used in Pharmaceutical Industry:
(2R, 4R)-4-HYDROXYTETRAHYDROFURAN-2-METHANOL is used as a building block for the synthesis of various pharmaceuticals due to its unique cyclic structure and reactivity, contributing to the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
(2R, 4R)-4-HYDROXYTETRAHYDROFURAN-2-METHANOL is used as a reagent in the synthesis of novel organic compounds, enabling the creation of a wide range of chemical products with diverse applications.
Used as a Solvent in Polymer Industry:
(2R, 4R)-4-HYDROXYTETRAHYDROFURAN-2-METHANOL is used as a solvent for polymers, facilitating the processing and manufacturing of various polymer-based materials.
Used in Biotechnology Research:
(2R, 4R)-4-HYDROXYTETRAHYDROFURAN-2-METHANOL is used as a research compound in biotechnology, where its unique structural properties and reactivity are leveraged to explore new applications and advancements in the field.
Check Digit Verification of cas no
The CAS Registry Mumber 164267-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,2,6 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 164267-53:
(8*1)+(7*6)+(6*4)+(5*2)+(4*6)+(3*7)+(2*5)+(1*3)=142
142 % 10 = 2
So 164267-53-2 is a valid CAS Registry Number.
164267-53-2Relevant academic research and scientific papers
Intramolecular addition of carbon radicals to aldehydes: synthesis of enantiopure tetrahydrofuran-3-ols
Tiecco, Marcello,Testaferri, Lorenzo,Marini, Francesca,Sternativo, Silvia,Santi, Claudio,Bagnoli, Luana,Temperini, Andrea
, p. 5482 - 5489 (2008/01/07)
A simple and efficient substrate-controlled asymmetric synthesis of enantiopure tetrahydrofuran-3-ols by a 5-exo-trig radical cyclization is described. This cyclization occurs when a δ-carbon radical adds intramolecularly to the carbonyl group of an aldeh
Enantiospecific total synthesis of L-2',3'-dideoxyisonucleosides via regioselective opening of optically active C2-symmetric 1,4-pentadiene bis- epoxide
Jung,Kretschik
, p. 2975 - 2981 (2007/10/03)
A new method for the synthesis of L-2',3'-dideoxyisonucleosides is described. The readily available, optically active C2-symmetric bis-epoxide (2S,4S)-1,2:4,5-diepoxypentane (5) was prepared by a short route from readily available starting mate
