149882-18-8 Usage
Uses
Used in Pharmaceutical Industry:
[(3S,5S)-5-(2,4-Difluoro-phenyl)-5-[1,2,4]triazol-1-ylmethyl-tetrahydro-furan-3-yl]-methanol is used as a building block for the development of new pharmaceutical compounds due to its complex structure and potential biological activity. Its unique features may allow for the creation of novel drugs with specific targeting or therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, [(3S,5S)-5-(2,4-Difluoro-phenyl)-5-[1,2,4]triazol-1-ylmethyl-tetrahydro-furan-3-yl]-methanol serves as a valuable intermediate or starting material for the synthesis of more complex molecules. Its diverse functional groups and chiral centers provide opportunities for further chemical modifications and the creation of a wide range of compounds with various applications.
Used in Medicinal Chemistry Research:
[(3S,5S)-5-(2,4-Difluoro-phenyl)-5-[1,2,4]triazol-1-ylmethyl-tetrahydro-furan-3-yl]-methanol is utilized in medicinal chemistry research to explore its potential as a therapeutic agent. [(3S,5S)-5-(2,4-Difluoro-phenyl)-5-[1,2,4]triazol-1-ylmethyl-tetrahydro-furan-3-yl]-methanol's unique structure may offer new avenues for the treatment of various diseases or conditions, and ongoing research aims to uncover its full potential in this area.
Check Digit Verification of cas no
The CAS Registry Mumber 149882-18-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,8,8 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 149882-18:
(8*1)+(7*4)+(6*9)+(5*8)+(4*8)+(3*2)+(2*1)+(1*8)=178
178 % 10 = 8
So 149882-18-8 is a valid CAS Registry Number.
149882-18-8Relevant academic research and scientific papers
Concise asymmetric routes to 2,2,4-trisubstituted tetrahydrofurans via chiral titanium imide enolates: Key intermediates towards synthesis of highly active azole antifungals Sch 51048 and Sch 56592
Saksena, Anil K.,Girijavallabhan, Viyyoor M.,Wang, Haiyan,Liu, Yi-Tsung,Pike, Russell E.,Ganguly, Ashit K.
, p. 5657 - 5660 (2007/10/03)
Two complimentary approaches to the key (-)-(2R)-cis-tosylate 1 and its (+)-(2S)-enantiomer 15 via generation of chiral imide enolates having a 2,2-disubstituted olefin functionality in the β-position, are described. In a 'protecting group free' sequence, reaction of the titanium enolate generated from (4R)-benzyl-2-oxazolidinone derived imide 5b with s-trioxane provided a convenient intermediate 19 which could be directly subjected to 2,4-diastereoselective iodocyclization.
