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1-m-Fluorbenzoyl-2-isopropyliden-hydrazin is a chemical compound with the molecular formula C11H13FN2O. It is a derivative of hydrazine, featuring a fluorobenzoyl group attached to the 1-position and an isopropyliden group at the 2-position. 1-m-Fluorbenzoyl-2-isopropyliden-hydrazin is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a building block for the synthesis of various biologically active molecules. Its structure provides a unique combination of functional groups that can be further modified to create a range of compounds with different properties and uses. The specific arrangement of the fluorine atom on the benzene ring and the isopropyliden group on the hydrazine moiety can influence the reactivity and selectivity of the compound in chemical reactions, making it a valuable intermediate in organic synthesis.

712-88-9

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712-88-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 712-88-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 712-88:
(5*7)+(4*1)+(3*2)+(2*8)+(1*8)=69
69 % 10 = 9
So 712-88-9 is a valid CAS Registry Number.

712-88-9Relevant academic research and scientific papers

Discovery of a novel series of indolyl hydrazide derivatives as diacylglycerol acyltransferase-1 inhibitors

Kim, Minkyoung,Kwon, Jinsun,Kim, Mun Ock,Singh, Sarbjit,Kim, Sang Kyum,Lee, Kyeong,Lee, Kiho,Lee, Hyun Sun,Choi, Yongseok

supporting information, p. 628 - 635 (2015/05/04)

A novel series of hydrazide derivatives were synthesized as potential diacylglycerol acyltransferase (DGAT) inhibitors. Among them, compounds 8u and 8v exhibited selective and potent DGAT-1 inhibitory activities. In addition, compound 8u dose-dependently inhibited triglyceride synthesis in HepG2 cell lines. Furthermore, treatment with compound 8u for an oral lipid tolerance test showed a significant decrease in plasma triglyceride levels compared with vehicle-treated control animals, indicating delayed absorption of triglyceride after an acute lipid challenge.

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