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Cyclohexanecarboxylic acid, 5-methyl-2-oxo-, ethyl ester, also known as ethyl 5-methyl-2-oxocyclohexanecarboxylate, is an organic compound with the chemical formula C10H16O3. It is a colorless liquid with a molecular weight of 184.23 g/mol. This ester is derived from cyclohexanecarboxylic acid, where a methyl group is attached at the 5th position and an oxo group is present at the 2nd position. The ethyl ester is formed by the esterification of the carboxylic acid group with ethanol. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain antibiotics and insecticides. The compound is characterized by its unique chemical structure, which contributes to its specific reactivity and applications in the chemical industry.

6134-75-4

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6134-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6134-75-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,3 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6134-75:
(6*6)+(5*1)+(4*3)+(3*4)+(2*7)+(1*5)=84
84 % 10 = 4
So 6134-75-4 is a valid CAS Registry Number.

6134-75-4Relevant academic research and scientific papers

Discovery of Novel Spiroindoline Derivatives as Selective Tankyrase Inhibitors

Shirai, Fumiyuki,Tsumura, Takeshi,Yashiroda, Yoko,Yuki, Hitomi,Niwa, Hideaki,Sato, Shin,Chikada, Tsubasa,Koda, Yasuko,Washizuka, Kenichi,Yoshimoto, Nobuko,Abe, Masako,Onuki, Tetsuo,Mazaki, Yui,Hirama, Chizuko,Fukami, Takehiro,Watanabe, Hirofumi,Honma, Teruki,Umehara, Takashi,Shirouzu, Mikako,Okue, Masayuki,Kano, Yuko,Watanabe, Takashi,Kitamura, Kouichi,Shitara, Eiki,Muramatsu, Yukiko,Yoshida, Haruka,Mizutani, Anna,Seimiya, Hiroyuki,Yoshida, Minoru,Koyama, Hiroo

, p. 3407 - 3427 (2019/04/17)

The canonical WNT pathway plays an important role in cancer pathogenesis. Inhibition of poly(ADP-ribose) polymerase catalytic activity of the tankyrases (TNKS/TNKS2) has been reported to reduce the Wnt/β-catenin signal by preventing poly ADP-ribosylation-

4-Hydroxy-2-quinolones 113. Synthesis and antitubercular activity of N-R-amides of 4-hydroxy-6-methyl-2-oxo-1-propyl-1,2,5,6,7,8-hexahydroquinoline- 3-carboxylic acid

Ukrainets,Kolesnik,Sidorenko,Gorokhova,Turov

, p. 326 - 333 (2008/09/21)

A preparative method has been developed and the synthesis has been effected of anilides and heterylamides of 4-hydroxy-6-methyl-2-oxo-1-propyl-1,2,5,6,7,8- hexahydroquinoline-3-carboxylic acid. A comparative analysis has been carried out of the structure and antitubercular properties of the synthesized compounds and their analogs unsubstituted in the quinoline nucleus.

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