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1-Fluoro-3-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-benzene is a complex organic compound with the molecular formula C9H5F7. It is a halogenated aromatic compound, characterized by the presence of fluorine atoms attached to a benzene ring. The molecule features a fluorine atom at the 1-position and a trifluoromethyl group (CF3) attached to the 2-position of the benzene ring. Additionally, a 2,2,2-trifluoro-1-trifluoromethyl-ethyl group is connected to the 3-position of the benzene ring, further enhancing its halogenated nature. 1-Fluoro-3-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-benzene is known for its unique chemical properties, such as high reactivity and stability, which make it useful in various chemical applications, including the synthesis of pharmaceuticals and agrochemicals. Due to its complex structure and multiple fluorine substitutions, it is also of interest in the field of materials science for the development of new compounds with specific physical and chemical characteristics.

26029-54-9

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26029-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26029-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,2 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26029-54:
(7*2)+(6*6)+(5*0)+(4*2)+(3*9)+(2*5)+(1*4)=99
99 % 10 = 9
So 26029-54-9 is a valid CAS Registry Number.

26029-54-9Downstream Products

26029-54-9Relevant academic research and scientific papers

Comparison of gas-phase acidities of some carbon acids with their rates of hydron exchange in methanolic methoxide

DeTuri, Vincent F.,Koch, Heinz F.,Koch, Judith G.,Lodder, Gerrit,Mishima, Masaaki,Zuilhof, Han,Abrams, Neal M.,Anders, Cecily E.,Biffinger, Justin C.,Han, Patrick,Kurland, Adam R.,Nichols, Jason M.,Ruminski, Anne M.,Smith, Patricia R.,Vasey, Karen D.

, p. 308 - 317 (2007/10/03)

Hydron exchange reaction rates, kexch M-1s -1, using methanolic sodium methoxide are compared with gas-phase acidities, ΔGAcid0 kcal/mol, for four 9-YPhenylfluorenes-9-iH, seven YC6/s

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