10374-28-4 Usage
Description
N,N-diethylcyclopropanecarboxamide is a chemical compound belonging to the carboxamide family, characterized by a carbonyl group and an amine group. It features a secondary alkyl amine, specifically diethylamine, and forms a cyclic structure with a cyclopropane ring. N,N-diethylcyclopropanecarboxaMide serves as a base structure for synthesizing more complex compounds, making it valuable in various industrial and pharmaceutical applications.
Uses
Used in Pharmaceutical Industry:
N,N-diethylcyclopropanecarboxamide is used as a base structure for the synthesis of complex compounds, which can be further utilized in the development of pharmaceutical products. Its cyclic nature allows for the creation of diverse molecules with potential therapeutic applications.
Used in Chemical Synthesis:
N,N-diethylcyclopropanecarboxamide is used as a starting material or intermediate in the synthesis of other complex organic compounds. Its unique structure enables the formation of various chemical bonds, making it a versatile component in the production of specialty chemicals.
Used in Research and Development:
N,N-diethylcyclopropanecarboxamide is employed as a research compound in academic and industrial laboratories. Its properties and reactivity are studied to understand its potential applications and to develop new synthetic methods for creating novel compounds.
It is important to handle N,N-diethylcyclopropanecarboxamide with care due to its chemical characteristics, ensuring safety and proper utilization in the intended applications.
Check Digit Verification of cas no
The CAS Registry Mumber 10374-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,7 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10374-28:
(7*1)+(6*0)+(5*3)+(4*7)+(3*4)+(2*2)+(1*8)=74
74 % 10 = 4
So 10374-28-4 is a valid CAS Registry Number.
10374-28-4Relevant articles and documents
Total Synthesis of Cardiolipins Containing Chiral Cyclopropane Fatty Acids
Inuki, Shinsuke,Ohta, Ippei,Ishibashi, Shunichi,Takamatsu, Masayuki,Fukase, Koichi,Fujimoto, Yukari
, p. 7832 - 7838 (2017)
Cardiolipin (CL) is a phospholipid located in both the eukaryotic mitochondrial inner membrane and the bacterial cell membrane. Some bacterial CLs are known to contain cyclopropane moieties in their acyl chains. Although the CLs are thought to be involved in the innate immune response, there have been few attempts at chemical synthesis of the CLs, and detailed studies of their biological activities are scarce. Thus, we have developed a synthetic route to CLs containing chiral cyclopropane moieties.
Ni-Al Bimetallic Catalyzed Enantioselective Cycloaddition of Cyclopropyl Carboxamide with Alkyne
Liu, Qi-Sheng,Wang, De-Yin,Yang, Zhi-Jun,Luan, Yu-Xin,Yang, Jin-Fei,Li, Jiang-Fei,Pu, You-Ge,Ye, Mengchun
supporting information, p. 18150 - 18153 (2017/12/27)
A Ni-Al bimetallic catalyzed enantioselective cycloaddition reaction of cyclopropyl carboxamides with alkynes has been developed. A series of cyclopentenyl carboxamides were obtained in up to 99% yield and 94% ee. The bifunctional-ligand-enabled bimetallic catalysis proved to be an efficient strategy for the C-C bond cleavage of unreactive cyclopropanes.
