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1,1,1-Trifluoro-pent-2-ene is a fluorinated organic compound with the molecular formula C5H5F3. It is a colorless liquid with a pungent odor and is characterized by the presence of three fluorine atoms attached to the first carbon atom of the pent-2-ene backbone. 1,1,1-trifluoro-pent-2-ene is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique reactivity and stability. It can be synthesized through various methods, such as the reaction of 1,1,1-trifluoro-2-butanol with phosphorus pentoxide or the dehydrofluorination of 1,1,1-trifluoro-3-pentanol. The compound's properties, such as its low boiling point, high reactivity, and resistance to hydrolysis, make it a valuable building block in the fluorochemical industry.

406-83-7

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406-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 406-83-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 406-83:
(5*4)+(4*0)+(3*6)+(2*8)+(1*3)=57
57 % 10 = 7
So 406-83-7 is a valid CAS Registry Number.

406-83-7Downstream Products

406-83-7Relevant academic research and scientific papers

Molybdenum chloride catalysts for Z-selective olefin metathesis reactions

Koh, Ming Joo,Nguyen, Thach T.,Lam, Jonathan K.,Torker, Sebastian,Hyvl, Jakub,Schrock, Richard R.,Hoveyda, Amir H.

, p. 80 - 85 (2017)

The development of catalyst-controlled stereoselective olefin metathesis processes has been a pivotal recent advance in chemistry. The incorporation of appropriate ligands within complexes based on molybdenum, tungsten and ruthenium has led to reactivity and selectivity levels that were previously inaccessible. Here we show that molybdenum monoaryloxide chloride complexes furnish higher-energy (Z) isomers of trifluoromethyl-substituted alkenes through cross-metathesis reactions with the commercially available, inexpensive and typically inert Z-1,1,1,4,4,4-hexafluoro-2-butene. Furthermore, otherwise inefficient and non-stereoselective transformations with Z-1,2-dichloroethene and 1,2-dibromoethene can be effected with substantially improved efficiency and Z selectivity. The use of such molybdenum monoaryloxide chloride complexes enables the synthesis of representative biologically active molecules and trifluoromethyl analogues of medicinally relevant compounds. The origins of the activity and selectivity levels observed, which contradict previously proposed principles, are elucidated with the aid of density functional theory calculations.

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