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2,3,5-Tri(trifluoromethyl)-n-nonafluorohexen(2) is a complex organic compound characterized by its unique structure and properties. It consists of a hexen(2) backbone, which is a six-carbon chain with a double bond between the second and third carbon atoms. This molecule is further distinguished by the presence of three trifluoromethyl groups (-CF3) attached to the 2nd, 3rd, and 5th carbon atoms. The compound is highly fluorinated, with nine fluorine atoms in total, contributing to its nonafluoro (nine fluorine) designation. The trifluoromethyl groups enhance the molecule's stability and reactivity, making it a potential candidate for various chemical applications, such as in the production of specialty chemicals or as an intermediate in the synthesis of fluorinated compounds. The compound's specific properties, such as its reactivity, volatility, and thermal stability, are influenced by the electronegativity and small size of the fluorine atoms, which can lead to unique interactions with other molecules.

2107-25-7

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2107-25-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2107-25-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,0 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2107-25:
(6*2)+(5*1)+(4*0)+(3*7)+(2*2)+(1*5)=47
47 % 10 = 7
So 2107-25-7 is a valid CAS Registry Number.

2107-25-7Upstream product

2107-25-7Downstream Products

2107-25-7Relevant academic research and scientific papers

?-BIS(BENZENE)CHROMIUM(0)-CATALYZED OLIGOMERIZATION OF PERFLUOROPROPYLENE

Huang, Yaozeng,Li, Jisen,Zhou, Jianqiang,Zhu, Zhongmu,Hou, Guoyu

, p. 185 - 191 (1981)

In the presence of zerovalent ?-bis(benzene)chromium(0) (I), perfluoropropylene (II) was found to undergo oligomerization under very mild conditions to dimers (b.p. 46 deg, M+, 300) and trimers (b.p. 100-102 deg C, M+ - 19, 431) in the ratio of 2.5-3.0 to 1.One mol of metal complex could catalyze the conversion of 50 mol of perfluoropropylene.One the basis of 19F NMR, the structures of the dimers are III and IV in a ratio of ca. 80/20 and the trimers V and VI; VII and VIII also seemed to be present.V/VI/(VII + VIII) is 80/10/4.In benzene solution, perfluoropropylene was shown not to be catalytically oligomerized by fluoride ion (KF, CrF2 of (CH3)4NF) (nor by monovalent ?-dibenzenechromium(I).A possible mechanism of the reaction was proposed.

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