556053-60-2 Usage
Uses
Used in Pharmaceutical Industry:
(2R,3S)-3-(4-FLUOROPHENYL)OXIRANE-2-CARBOXAMIDE is used as a potential candidate for medicinal chemistry research due to its unique properties and reactivity. Its oxirane-2-carboxamide structure suggests potential functionality that could be of interest for the development of new drugs.
Used in Agrochemical Industry:
(2R,3S)-3-(4-FLUOROPHENYL)OXIRANE-2-CARBOXAMIDE may have potential applications in the agrochemical industry, where it could be used as a building block for the synthesis of biologically active molecules with pesticidal or herbicidal properties.
Used in Materials Science:
(2R,3S)-3-(4-FLUOROPHENYL)OXIRANE-2-CARBOXAMIDE may also have potential applications in materials science, where its unique properties could be utilized in the development of new materials with specific characteristics.
Further studies on the properties and potential uses of (2R,3S)-3-(4-FLUOROPHENYL)OXIRANE-2-CARBOXAMIDE are warranted to fully explore its applications in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 556053-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,6,0,5 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 556053-60:
(8*5)+(7*5)+(6*6)+(5*0)+(4*5)+(3*3)+(2*6)+(1*0)=152
152 % 10 = 2
So 556053-60-2 is a valid CAS Registry Number.
556053-60-2Relevant academic research and scientific papers
Wang, Mei-Xiang,Lin, Shuang-Jun,Liu, Chu-Sheng,Zheng, Qi-Yu,Li, Ji-Sheng
, p. 4570 - 4573 (2003)
Catalyzed by a nitrile hydratase/amidase-containing microbial Rhodococcus sp. AJ270 whole-cell catalyst, a number of racemic trans-2,3-epoxy-3-arylpropanenitriles 1 underwent rapid and efficient hydrolysis under very mild conditions to afford 2R,3S-2-arylglycidamides 2 in excellent yield with enantiomeric excess higher than 99.5%. The overall enantioselectivity of the biotransformations originated from the combined effects of a dominantly high 2S-enantioselective amidase and low 2S-enantioselective nitrile hydratase involved in the cell. The influence of the substrates on both reaction efficiency and enantioselectivity was also discussed in terms of steric and electronic effects.
