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Pentafluoro-n-butylbenzene is an organic compound with the molecular formula C10H5F5. It is a derivative of benzene, where one hydrogen atom is replaced by a butyl group (a four-carbon chain), and five fluorine atoms are attached to the benzene ring. pentafluoro-n-butylbenzene is characterized by its high electronegativity and lipophilicity due to the presence of fluorine atoms, which can influence its chemical reactivity and physical properties. Pentafluoro-n-butylbenzene is used in various applications, including as a solvent, a chemical intermediate, and in the synthesis of pharmaceuticals and agrochemicals. Its unique properties make it a valuable compound in the field of organic chemistry and materials science.

715-61-7

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715-61-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 715-61-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 715-61:
(5*7)+(4*1)+(3*5)+(2*6)+(1*1)=67
67 % 10 = 7
So 715-61-7 is a valid CAS Registry Number.

715-61-7Downstream Products

715-61-7Relevant academic research and scientific papers

Unexpected distinction in reactivity of pentafluorobenzenesulfonyl halides toward organolithiums and organomagnesium halides

Bardin, Vadim V.,Maksimov, Alexander M.

, p. 731 - 737 (2017/10/16)

C6F5SO2Cl reacts with organolithiums and organomagnesium halides RM (R = Me, Bu, Ph; M = Li, MgX) to give mainly C6F5H and C6F5Cl. C6F5SO2Br and

Transition-metal-free synthesis of fluorinated arenes from perfluorinated arenes coupled with grignard reagents

Sun, Yunqiang,Sun, Hongjian,Jia, Jiong,Du, Aiqin,Li, Xiaoyan

supporting information, p. 1079 - 1081 (2014/03/21)

A simple method to obtain organofluorine compounds from perfluorinated arenes coupled with Grignard reagents in the absence of a transition-metal catalyst was reported. In particular, the perfluorinated arenes could react not only with aryl Grignard reagents but also with alkyl Grignard reagents in moderate to good yields.

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