556053-62-4 Usage
Uses
Used in Medicinal Chemistry:
(2R,3S)-3-(4-CHLOROPHENYL)OXIRANE-2-CARBOXAMIDE is used as a compound with potential applications in medicinal chemistry due to its structural features and reactivity. Its unique arrangement of functional groups may allow for the development of new pharmaceutical agents or the modification of existing ones.
Used in Organic Synthesis:
In the field of organic synthesis, (2R,3S)-3-(4-CHLOROPHENYL)OXIRANE-2-CARBOXAMIDE can be utilized as a building block or intermediate for the synthesis of more complex organic molecules. Its epoxy and carboxamide groups may enable the formation of new chemical bonds and the creation of diverse molecular structures.
Used in Research and Experimentation:
(2R,3S)-3-(4-CHLOROPHENYL)OXIRANE-2-CARBOXAMIDE is also used in research and experimentation to further explore its properties and possible uses. Through systematic studies, scientists can gain a deeper understanding of its reactivity, stability, and potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 556053-62-4 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 556053-62:
(8*5)+(7*5)+(6*6)+(5*0)+(4*5)+(3*3)+(2*6)+(1*2)=154
154 % 10 = 4
So 556053-62-4 is a valid CAS Registry Number.
556053-62-4Relevant academic research and scientific papers
5-(α-Halobenzyl)- and 5-Benzylidene-2,2-dimethyl-1,3-oxazolidin-4-ones in Synthesis of α-Hydroxy Acids
Mamedov,Mamedova,Khikmatova,Korshin,Sinyashin
, p. 2801 - 2809 (2018/02/21)
The reactions of acid hydrolysis of 5-(α-halobenzyl)- and 5-benzylidene-2,2-dimethyl-1,3-oxazolidin-4-ones were studied. A possibility of the synthesis of corresponding α-hydroxy acids was shown.
Nitrile biotransformations for highly efficient and enantioselective syntheses of electrophilic oxiranecarboxamides
Wang, Mei-Xiang,Lin, Shuang-Jun,Liu, Chu-Sheng,Zheng, Qi-Yu,Li, Ji-Sheng
, p. 4570 - 4573 (2007/10/03)
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.
