382-12-7

Usage

Uses

Used in Organic Synthesis:
3,3-Dibromo-2-oxo-1,1,1-trifluorobutane is utilized as a building block in the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable component in creating a range of chemical products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3,3-Dibromo-2-oxo-1,1,1-trifluorobutane is employed as a reagent in chemical reactions. Its properties allow it to contribute to the development of new pharmaceuticals, aiding in the advancement of drug discovery and design.
Used in Laboratory Settings:
Due to its reactivity, 3,3-Dibromo-2-oxo-1,1,1-trifluorobutane is commonly handled with caution in laboratory settings. It is used for educational purposes and research, where its properties can be studied and harnessed for various scientific applications.

Upstream product

• 381-88-4 1,1,1-trifluoro-2-butanone 
• 382-01-4 3-bromo-1,1,1-trifluoro-2-butanone 

Downstream Products

• 143309-87-9 6,7-dichloro-2-(trifluoromethyl)-3-methylquinoxaline 
• 131549-62-7 1,1,1-trifluoro-2,3-butanedione 
• 188490-63-3 3,3,3-trifluoro-2-oxopropanal 1-(4-chloro-2-fluoro-5-hydroxyphenylhydrazone) 

Relevant academic research and scientific papers

PYRAZOLE DERIVATIVES HAVING KINASE MODULATING ACTIVITY

The invention provides a compound of the formula (I): or a salt, tautomer, N-oxide or solvate thereof; wherein A is selected from a bond, CH2 and CH(CN); Rl is selected from: (i) a cycloalkyl group of 3 to 6 ring members optionally substituted by one or more substituents selected from methyl, ethyl, hydroxy, methoxy, ethoxy, fluorine, amino and cyano; (ii) a phenyl group optionally substituted by up to three substituents selected from methyl, ethyl, fluorine, chlorine, methoxy, ethoxy and methylsulphonyl, but excluding 2,6-difluorophenyl, 2-fluoro-6-methoxy and 5-chloro-2-methoxyphenyl; (iii) a monocyclic heterocyclic group selected from furyl and isoxazolyl, the heterocyclic group being optionally substituted by one or two groups selected from methyl, ethyl, and a group CH2R2 where R2 is a five or six membered saturated heterocyclic ring containing one or two heteroatom ring members selected from O and N, the heterocyclic ring being optionally substituted by one or two methyl groups; and (iv) a bicyclic heterocyclic group selected from 2,3-dihydrobenzofuranyl and benzo[c]isoxazolyl, the bicyclic group being optionally substituted by one or two substituents selected from methyl, ethyl, hydroxy, methoxy, ethoxy, fluorine, amino, cyano and chlorine, the bicyclic heterocyclic group being other than a 2,2-dimethyl-2,3-dihydrobenzofuran-7-yl group.

Pyridazin-3-one derivatives, their use, and intermediates for their production

Novel hydrazones of formula [2] having the following structural formula are provided, which are useful intermediates to form active ingredients of herbicides, wherein R3 is hydrogen, alkyl, haloalkyl, or alkoxy alkyl; and Q is [Q-1], [Q-2], [Q-

Pyridazin-3-one derivatives, their use, and intermediates for their production

PCT No. PCT/JP96/02311 Sec. 371 Date Jan. 30, 1998 Sec. 102(e) Date Jan. 30, 1998 PCT Filed Aug. 19, 1996 PCT Pub. No. WO97/07104 PCT Pub. Date Feb. 27, 1997Novel pyridazin-3-one derivatives of formula [1] are provided, which are useful as active ingredie

19F NMR Studies on the Mechanism of Riboflavin Synthase. Synthesis of 6-(Trifluoromethyl)-7-oxo-8-(D-ribityl)lumazine and 6-(trifluoromethyl)-7-methyl-8-(D-ribityl)lumazine

The reactions of hexafluoropropene oxide (19), methyl trifluoropyruvate (21), and 1,1,1-trifluorobutane-2,3-dione (45) with a series of ortho diamines were investigated as an approach to the synthesis of trifluoromethyl-substituted quinoxalinones and luma