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4,5,6-trichloro-1,3-bis(trifluoromethyl)benzene is a synthetic organic compound characterized by its unique molecular structure. It features a benzene ring with three chlorine atoms at positions 4, 5, and 6, and two trifluoromethyl groups attached at positions 1 and 3. 4,5,6-trichloro-1,3-bis(trifluoromethyl)benzene is known for its stability and resistance to chemical reactions due to the presence of electron-withdrawing chlorine and trifluoromethyl groups. These groups also contribute to the compound's lipophilic nature, making it soluble in nonpolar solvents. The compound has potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science, where its specific properties can be exploited for specific purposes. However, due to its complex structure and potential environmental impact, it is important to handle and dispose of this chemical responsibly.

327-72-0

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327-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 327-72-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 327-72:
(5*3)+(4*2)+(3*7)+(2*7)+(1*2)=60
60 % 10 = 0
So 327-72-0 is a valid CAS Registry Number.

327-72-0Relevant academic research and scientific papers

A New Trifluoromethylating Agent: Synthesis of Polychlorinated (Trifluoromethyl)benzenes and 1,3-Bis(trifluoromethyl)benzenes and Conversion into Their Trichloromethyl Counterparts and Molecular Structure of Highly Strained Polychloro-m-xylenes

Castaner, J.,Riera, J.,Carilla, J.,Robert, A.,Molins, E.,Miravitlles, C.

, p. 103 - 110 (2007/10/02)

Mixtures of CCl3F and AlCl3 replace CF3 for H in polychlorobenzenes.Thus, by treatment of a solution of the suitable polychlorobenzene in CCl3F with AlCl3, the following compounds can be prepared: pentachloro- (2), 2,3,4,5-tetrachloro- (5), 2,3,4,6-tetrachloro- (8), 2,3,5,6-tetrachloro- (11), 2,3,4-trichloro- (14), 2,4,5-trichloro- (17), and 2,4,6-trichloro-1-(trifluoromethyl)benzene (20), as well as 4,5,6-trichloro- (31) and 2,4,6-trichloro-1,3-bis(trifluoromethyl)benzene (32).The reaction of the above-mentioned trifluoromethylated compounds with AlCl3 in CS2 yieldstheir trichloromethyl counterparts: 3, 6, 9, 12, 15, 18, 21, 34, and 36.The chlorination of 32 or 36 by means of Silberrad's reagent (SO2Cl2, AlCl3, and S2Cl2) affords perchloro-m-xylene (38), a new highly strained chlorocarbon whose synthesis was attempted repeatedly in the past. 9, 15, 17, and 21, when treated with oleum and then with water, are converted into 2,3,4,6-tetrachloro- (22), 2,3,4-trichloro- (23), 2,4,5-trichloro- (24), and 2,4,6-trichlorobenzoic acid (25), respectively; under similar treatment, 34, 36, and 38 give 4,5,6-trichloro- (33), 2,4,5-trichloro- (35), and tetrachloroisophthalic acid (39), respectively.The formation of the (trifluoromethyl)benzenes is discussed, and in this connection it has been found that CCl3F solutions of 3 and 18 in the presence of AlCl3 give back 2 and 17, respectively.Molecular structures of highly strained m-xylenes 36 and 38, as well as that of the much less strained 34, ascertained by X-ray analysis, are reported and commented.IR, UV, and NMR spectral data of the compounds synthesized are presented.The interesting UV spectrum of 21 is discussed.

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