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αH-Pentadecachlorotriphenylmethane is a complex organic compound with the molecular formula C19Cl15. It is a derivative of triphenylmethane, where three hydrogen atoms on the central carbon atom are replaced by chlorine atoms, resulting in a highly chlorinated molecule. αH-Pentadecachlorotriphenylmethane is characterized by its high stability and resistance to degradation, which can be attributed to the presence of multiple chlorine atoms. It is not a naturally occurring substance and is typically synthesized for specific applications in chemical research or as a reference compound in studies related to the effects of chlorination on organic molecules. Due to its highly chlorinated nature, it is important to handle such compounds with care, as they may have potential environmental and health implications.

33240-61-8

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33240-61-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33240-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,4 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33240-61:
(7*3)+(6*3)+(5*2)+(4*4)+(3*0)+(2*6)+(1*1)=78
78 % 10 = 8
So 33240-61-8 is a valid CAS Registry Number.

33240-61-8Relevant academic research and scientific papers

Preparation and characterization of persistent maltose-conjugated triphenylmethyl radicals

Mesa, Juan Antonio,Velazquez-Palenzuela, Amado,Brillas, Enric,Coll, Josep,Torres, Josep Lluis,Julia, Luis

, p. 1081 - 1086 (2012)

The condensation reaction of d-maltose to free radicals of the series of tris(2,4,6-trichlorophenyl)methyl (TTM) and tris(perchlorophenyl)methyl (PTM) has been described for the first time. The new persistent radicals 1 and 2 are very stable and have been

SYNTHESIS AND PROPERTIES OF THE 1/1 COMPLEX OF 1,4,7,10,13,16-HEXAOXACYCLOOCTADECANE WITH POTASSIUM PERCHLOROTRIPHENYLMETHIDE

Veciana, J.,Riera, J.,Castaner, J.,Ferrer, N.

, p. 131 - 142 (1985)

The 1/1 complex of 1,4,7,10,13,16-hexaoxacyclooctadecane with potassium perchlorotriphenylmethide has been prepared by reaction, in the presence of 18-crown-6, of (C6Cl5)3CH with KOH or reduction of radical (C6Cl5)3 with K metal.Its structure as reveal

Chemical Modification toward Long Spin Lifetimes in Organic Conjugated Radicals

Dai, Ya-Zhong,Dong, Bo-Wei,Kao, Yi,Wang, Zi-Yuan,Un, Hio-Ieng,Liu, Zheng,Lin, Zhi-Jun,Li, Liang,Xie, Fang-Bai,Lu, Yang,Xu, Mei-Xing,Lei, Ting,Sun, Yu-Jie,Wang, Jie-Yu,Gao, Song,Jiang, Shang-Da,Pei, Jian

, p. 2972 - 2977 (2018/09/25)

Organic semiconductors for spin-based devices require long spin relaxation times. Understanding their spin relaxation mechanisms is critical to organic spintronic devices and applications for quantum information processing. However, reports on the spin re

Stable polyradicals with high-spin ground states. 1, synthesis, separation, and magnetic characterization of the stereoisomers of 2,4,5,6-tetrachloro-α, α, α', α'-tetrakis(pentachlorophenyl)-m-xylylene biradical

Veciana, Jaume,Rovira, Concepció,Crespo, Maria I.,Armet, Olga,Domingo, Victor M.,Palacio, Fernando

, p. 2552 - 2561 (2007/10/02)

Biradical 3 and its corresponding monoradical 6 have been synthesized and isolated as stable solids at ambient conditions. Biradical 3 exists in three stereoisomeric forms due to restricted correlated rotation of the aryl groups. It has obtained as a 60:4

Photochemistry of Stable Free Radicals: The Photolysis of Perchlorotriphenylmethyl Radicals

Fox, Marye Anne,Gaillard, Elizabeth,Chen, Chia-Chung

, p. 7088 - 7094 (2007/10/02)

The excitation of perchlorotriphenylmethyl radical (PTM) at 532 nm leads to an excited doublet, 2PTM* (τ = 7 ns).The lifetime of this state is insensitive to oxygen, electron acceptors, and hydrogen-donating solvents.Electron donors

An Easy, High-yield Synthesis of Highly Chlorinated Mono-, Di- and Triarylmethanes

Ballester, Manuel,Riera, Juan,Castaner, Juan,Rovira, Concepcion,Armet, Olag

, p. 64 - 66 (2007/10/02)

A simple, direct, high-yield Friedel-Crafts synthesis of highly chlorinated, overcrowded αH-aryl, αH-diaryl, and αH-triarylmethanes is described.The latter compounds are most valuable chemical precursors of inert free radicals, which are frequently obtain

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