53712-75-7 Usage
Uses
Used in Pharmaceutical Industry:
4-Cyclopropyl-4-oxobutyric acid is used as a synthetic intermediate for the production of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into the development of new drugs, enhancing their efficacy and therapeutic potential.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Cyclopropyl-4-oxobutyric acid serves as a key intermediate in the synthesis of various agrochemicals. Its reactivity and chemical properties make it suitable for the creation of effective pesticides and other agricultural chemicals.
Used in Organic Synthesis:
4-Cyclopropyl-4-oxobutyric acid is utilized as a building block in organic synthesis, enabling the creation of a wide range of compounds. Its versatility and reactivity make it a valuable component in the synthesis of complex organic molecules for various applications.
Used in Chemical Research:
Due to its unique chemical properties, 4-Cyclopropyl-4-oxobutyric acid is also employed in chemical research to explore new reactions and develop innovative synthetic methods. Its reactivity and structural features provide researchers with opportunities to investigate novel chemical transformations and mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 53712-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,1 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53712-75:
(7*5)+(6*3)+(5*7)+(4*1)+(3*2)+(2*7)+(1*5)=117
117 % 10 = 7
So 53712-75-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O3/c8-6(5-1-2-5)3-4-7(9)10/h5H,1-4H2,(H,9,10)
53712-75-7Relevant academic research and scientific papers
Asymmetric Strecker reaction of γ-keto acids. Facile entry to α-substituted and α,γ-disubstituted glutamic acids
Tang, Guozhi,Tian, Hongqi,Ma, Dawei
, p. 10547 - 10552 (2007/10/03)
The Strecker reaction of γ-keto acid derived sodium salts with (S)-phenylglycinol followed by treatment of the resultant α-amino nitriles with methanolic HCl and heating at 200°C give bicyclic lactones 11 and 12. Hydrolysis and subsequent debenzylation of
