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4,4,4-Trifluoro-1-(benzo-[b]-thiophen-3-yl)butane-1,3-dione, also known as 4,4,4-trifluoro-1-(benzo[b]thiophen-3-yl)-1,3-butanedione, is a chemical compound with the molecular formula C11H7F3OS. It is a white crystalline solid that is soluble in organic solvents. 4,4,4-TRIFLUORO-1-(BENZO-[B]-THIOPHEN-3-YL)BUTANE-1,3-DIONE is characterized by the presence of a trifluoromethyl group, a benzo[b]thiophene ring, and a butane-1,3-dione moiety. It is used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural features and reactivity. The compound's properties, such as its stability and electronic effects, make it a valuable building block in the development of new molecules with potential applications in various industries.

392-29-0

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392-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 392-29-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 392-29:
(5*3)+(4*9)+(3*2)+(2*2)+(1*9)=70
70 % 10 = 0
So 392-29-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H7F3O2S/c13-12(14,15)11(17)5-9(16)8-6-18-10-4-2-1-3-7(8)10/h1-4,6H,5H2

392-29-0Downstream Products

392-29-0Relevant academic research and scientific papers

Synthesis and luminescence-spectral properties of benzoheterocyclic β-diketones and their complexes with europium

Kostryukova,Ivanovskaya,Lyamin,Romanov,Osin,Zatonsky,Vasil'ev

experimental part, p. 455 - 460 (2012/06/16)

In order to solve some environmental and biomedical problems, we synthesized fluorinated heterocyclic β-diketones and estimated the luminescence-spectral properties of these compounds complexes with the ions of rare-earth elements as the possible reagents

Synthesis and biological evaluation of the 1,5-diarylpyrazole class of cyclooxygenase-2 inhibitors: Identification of 4-[5-(4-methylphenyl)- 3(trifluoromethyl)-1h-pyrazol-1-yl]benzenesulfonamide (sc-58635, celecoxib)

Penning, Thomas D.,Talley, John J.,Bertenshaw, Stephen R.,Carter, Jeffery S.,Collins, Paul W.,Docter, Stephen,Graneto, Matthew J.,Lee, Len F.,Malecha, James W.,Miyashiro, Julie M.,Rogers, Roland S.,Rogier,Yu, Stella S.,Anderson, Gary D.,Burton, Earl G.,Cogburn, J. Nita,Gregory, Susan A.,Koboldt, Carol M.,Perkins, William E.,Seibert, Karen,Veenhuizen, Amy W.,Zhang, Yan Y.,Isakson, Peter C.

, p. 1347 - 1365 (2007/10/03)

A series of sulfonamide-containing 1,5-diarylpyrazole derivatives were prepared and evaluated for their ability to block cyclooxygenase-2 (COX-2) in vitro and in vivo. Extensive structure-activity relationship (SAR) work was carried out within this series, and a number of potent and selective inhibitors of COX-2 were identified. Since an early structural lead (1f, SC- 236) exhibited an unacceptably long plasma half-life, a number of pyrazole analogs containing potential metabolic sites were evaluated further in vivo in an effort to identify compounds with acceptable pharmacokinetic profiles. This work led to the identification of 1i (4-[5-(4-methylphenyl)-3- (trifluoromethyl)-1H-pyrazol-1-y1]benzenesulfonamide, SC-58635, celecoxib), which is currently in phase III clinical trials for the treatment of rheumatoid arthritis and osteoarthritis.

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