188481-45-0 Usage
Uses
Used in Pharmaceutical Industry:
(R)-A-HYDROXY-3-FURANACETONITRILE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties. Its role in the production of chiral compounds is particularly valuable, as chirality is a critical factor in the efficacy and safety of many medications.
Used in Agrochemical Industry:
In the agrochemical sector, (R)-A-HYDROXY-3-FURANACETONITRILE is utilized as an intermediate in the creation of agrochemicals, such as pesticides and herbicides. Its involvement in the synthesis process helps in designing more effective and targeted agrochemicals to improve crop protection and yield.
Used as a Reagent in Organic Chemical Reactions:
(R)-A-HYDROXY-3-FURANACETONITRILE also serves as a reagent in various organic chemical reactions, facilitating the formation of desired products and enhancing the efficiency of synthesis processes. Its application in this area underscores its importance in the broader field of organic chemistry.
Overall, (R)-A-HYDROXY-3-FURANACETONITRILE's multifaceted applications across different industries highlight its significance as a versatile and valuable chemical compound in modern science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 188481-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,4,8 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 188481-45:
(8*1)+(7*8)+(6*8)+(5*4)+(4*8)+(3*1)+(2*4)+(1*5)=180
180 % 10 = 0
So 188481-45-0 is a valid CAS Registry Number.
188481-45-0Relevant academic research and scientific papers
Stereoselective synthesis of thienyl and furyl analogues of ephedrine
Effenberger, Franz,Eichhorn, Joachim
, p. 469 - 476 (2007/10/03)
The stereoselective syntheses of thienyl and furyl analogues of ephedrine starting from (R)- and (S)-cyanohydrins, respectively, are described. Addition of methyl Grignard to the O-trimethylsilyl protected optically active cyanohydrins (R)- and (S)-3 and hydrogenation of the resulting imino intermediates gives the erythro-2-amino alcohols 4 with high diastereoselectivity. Their reductive methylation leads to the enantiomerically pure thiophene analogues (1S,2S)- and (1R,2R)-6a, (1R,2S)- and (1S,2R)-6b as well as to the furan analogues (1S,2S)-6c and (1R,2S)-6d of ephedrine, The biological activity of the new compounds is under investigation.
Ueber die erste rekombinante Hydroxynitril-Lyase und ihre Anwendung in der Synthese von (S)-Cyanhydrinen
Foerster, Siegfried,Roos, Juergen,Effenberger, Franz,Wajant, Harald,Sprauer, Achim
, p. 493 - 494 (2007/10/03)
Keywords: Asymmetrische Synthesen; (S)-Cyanhydrine; Enzymkatalyse; Lyasen
