981-87-3 Usage
Description
2,4,6-Trichloro-1,3,5-triphenylborazine, a boron-nitrogen heterocycle with the chemical formula C18H12BCl3N2, is a white to light yellow crystalline solid. It is insoluble in water but soluble in organic solvents. 2.4.6-TRICHLORO-1.3.5-TRIPHENYLBORAZINE belongs to the family of borazines and is known for its boron-nitrogen bond.
Uses
Used in Organic Synthesis:
2,4,6-Trichloro-1,3,5-triphenylborazine is used as a reagent in organic synthesis for its unique boron-nitrogen heterocycle structure, which can be utilized in the formation of various complex organic compounds.
Used as a Precursor for Functional Materials:
Due to its chemical properties, 2,4,6-Trichloro-1,3,5-triphenylborazine serves as a precursor for the development of functional materials with specific applications in different industries.
Used in Coordination Chemistry:
The presence of the boron-nitrogen bond makes 2,4,6-Trichloro-1,3,5-triphenylborazine a valuable component in coordination chemistry, where it can be used to form metal-organic complexes.
Used as a Ligand in Metal-Organic Complexes:
2,4,6-Trichloro-1,3,5-triphenylborazine functions as a ligand in metal-organic complexes, contributing to the stability and properties of these complexes for various applications.
Used in Optoelectronics:
With its potential applications in the field of optoelectronics, 2,4,6-Trichloro-1,3,5-triphenylborazine can be utilized in the development of electronic devices and components that rely on the interaction of light and electronic properties.
Used in Materials Science:
In materials science, 2,4,6-Trichloro-1,3,5-triphenylborazine has potential uses in the creation of new materials with unique properties, such as high thermal stability, electrical conductivity, or optical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 981-87-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,8 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 981-87:
(5*9)+(4*8)+(3*1)+(2*8)+(1*7)=103
103 % 10 = 3
So 981-87-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H15B3Cl3N3/c22-25-19(16-10-4-1-5-11-16)26(23)21(18-14-8-3-9-15-18)27(24)20(25)17-12-6-2-7-13-17/h1-15H
981-87-3Relevant articles and documents
BORAZENE DERIVATIVES
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Page/Page column 38, (2012/10/08)
The present invention is directed to new borazene derivatives and their use in the manufacture of electronic devices, in particular electroluminescent and semiconductor devices. More specifically, the present invention relates to new stable borazene derivatives comprising boron atoms substituted by aryl groups and to their use in one or more layers of an electroluminescent or a semiconductor device, in particular in the emissive layer of organic light-emitting devices (OLED).
HETEROCYCLES RELATED TO 2,4-DIBORA 1,3-DIAZAROBENZENE
Allaoud, Smail,Frange, Bernard
, p. 129 - 136 (2007/10/02)
The reaction of ortho-substituted arylamines oY-C6H4NH2 (Y=H, Cl, Br, Me) with BX3, (X=F, Cl, Br, I) was investigated.By suitable choice of Y and X, this reaction may be directed to obtain, in a quantitative way, a new kind of heterocycle I instead of the expected trimeric species (oYC6H4NBX)3.The formation of I was found to be related to the bulk of Y substituent and to the nature of X, increasing in the order BCl3 a tertiary amine added, always gives the corresponding borazines.Some derivatives of I were prepared (X=Me, Y=Br, Me) and characterized by NMR (1H, 13C and 11B) and mass spectra. In connection with this study, we were led to the question of atropisomerism in the N-triarylborazines (oYC6H4NBX)3 when the starting arylamine bears an ortho substituent Y.As far as the compound Y=Me, X=Me is concerned, a sole isomer, the C3t one, could be obtained instead of the two expected.
