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Tris(4-(bromomethyl)phenyl)methane, also known as 1,3,5-tribromomethylbenzene, is an organic compound with the chemical formula C9H9Br3. It is a white crystalline solid that is soluble in organic solvents. Tris<4-(brommethyl)phenyl>methan is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed in the production of polymers and resins. Due to its reactive bromine atoms, it can undergo a variety of chemical reactions, making it a versatile building block in organic synthesis.

81399-99-7

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81399-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81399-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,9 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81399-99:
(7*8)+(6*1)+(5*3)+(4*9)+(3*9)+(2*9)+(1*9)=167
167 % 10 = 7
So 81399-99-7 is a valid CAS Registry Number.

81399-99-7Relevant academic research and scientific papers

Fluorescent tris-imidazolium sensors for picric acid explosive

Roy, Bijan,Bar, Arun Kumar,Gole, Bappaditya,Mukherjee, Partha Sarathi

, p. 1306 - 1310 (2013)

Two new anthracene-functionalized fluorescent tris-imidazolium salts have been synthesized, characterized, and proven to be selective sensors for picric acid, which is a common constituent of many powerful explosives. Theoretical studies revealed an unusual ground-state electron transfer from picrate anion to the sensor molecules.

Methylium ions with OPV chains - New NIR dyes

Meier, Herbert,Kim, Soungkyoo

, p. 1163 - 1167 (2007/10/03)

Carbinols, which contain three OPV chains, were generated in convergent syntheses. The extension of the conjugation leads to a bathochromic effect that shifts the absorption from the UV into the visible region. The carbinol series has a convergence limit

Dreifach verklammerte Triphenylmethyl-Radikale und -Kationen

Karbach, Stefan,Voegtle, Fritz

, p. 427 - 434 (2007/10/02)

Starting with 12, the diol 4 is obtained in a many-step synthesis.Reduction of 7, prepared from 4 with H2SO4, with VCl2 gives rise to the formation of radicals of type 1, which exhibit low stability in solution.Cations of the type 7, 11 are investigated b

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