188772-83-0 Usage
Uses
Used in Pharmaceutical Industry:
Benzamide, N-[1-(2-furanyl)-2,2-dimethylpropyl]-, (S)is used as a potential pharmaceutical agent for its potential anticancer, antifungal, or antimicrobial properties. Its unique structure and stereochemistry may contribute to its biological activity, making it a promising candidate for further research and development in the pharmaceutical field.
Used in Research and Development:
Benzamide, N-[1-(2-furanyl)-2,2-dimethylpropyl]-, (S)is used in research and development for understanding its properties, pharmacological effects, and potential applications. Further studies are needed to fully explore its potential uses and to optimize its therapeutic efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 188772-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,7,7 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 188772-83:
(8*1)+(7*8)+(6*8)+(5*7)+(4*7)+(3*2)+(2*8)+(1*3)=200
200 % 10 = 0
So 188772-83-0 is a valid CAS Registry Number.
188772-83-0Relevant academic research and scientific papers
Asymmetric synthesis of α-(heteroaryl)alkylamines and α-amino acids via nucleophilic 1,2-addition of lithiated heterocycles to aldehyde SAMP-hydrazones
Enders, Dieter,Del Signore, Giuseppe,Raabe, Gerhard
, p. 492 - 518 (2013/08/23)
The asymmetric synthesis of α-(heteroaryl)alkylamines was accomplished by employing a diastereoselective nucleophilic 1,2-addition of lithiated aromatic heterocycles to aldehyde SAMP-hydrazones, followed by BH 3·THF or SmI2 promoted removal of the chiral auxiliary. The CBz or benzoyl-protected amines were obtained in good yields (40%-78%) and excellent enantiomeric excesses (ee = 88%-99%). The methodology can be applied to the synthesis of highly enantioenriched α-amino acids (ee = 90%-99%). TUeBITAK.
