703-86-6

Basic information

• Product Name: 2,4,6-trichloro-1,3,5-trimethylborazine
• Synonyms: 2,4,6-Trichloro-1,3,5-trimethylborazine; borazine, 2,4,6-trichloro-1,3,5-trimethyl-
• CAS NO: 703-86-6
• Molecular Formula: C₃H₉B₃Cl₃N₃
• Molecular Weight: 225.9157
• Mol File: 703-86-6.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 181.8°C at 760 mmHg
• Flash Point: 63.8°C
• Density: 1.24g/cm³
• Vapor Pressure: 0.835mmHg at 25°C
• Refractive Index: 1.469
• CAS DataBase Reference: 2,4,6-trichloro-1,3,5-trimethylborazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-trichloro-1,3,5-trimethylborazine(703-86-6)
• EPA Substance Registry System: 2,4,6-trichloro-1,3,5-trimethylborazine(703-86-6)

Safety Data

• Hazardous Substances Data: 703-86-6(Hazardous Substances Data)

Usage

General Description

2,4,6-trichloro-1,3,5-trimethylborazine is a chemical compound with the molecular formula C3H6BCl3N3. It is a boron-containing heterocyclic compound and belongs to the class of borazines. 2,4,6-trichloro-1,3,5-trimethylborazine is a colorless liquid that has a strong and distinctive smell. Its main use is as a precursor in the production of boron nitride films, which have applications in electronics, optics, and other advanced materials. It is also used as a reagent in organic synthesis, particularly in the formation of boron-nitrogen bonds. Additionally, it has been investigated for potential applications in flame-retardant materials due to its high thermal stability and ability to inhibit the spread of flames. Overall, 2,4,6-trichloro-1,3,5-trimethylborazine plays a significant role in the development of advanced materials and has potential benefits in various industrial applications.

Upstream product

• 810670-92-9 chloro-methyl-methylamino-borane 
• 74-89-5 methylamine 
• 7647-01-0 hydrogenchloride 
• 877-07-6 hexamethylborazine 
• 250610-83-4 dichloro[dimethyphenylsilyl(methyl)amino]borane 
• 27151-95-7 Dichlorboryl-(trimethylsilyl)-methylamin 
• 18089-55-9 Cl₂BN(CH₃)(SiH₃) 
• 37936-22-4 BCl₂(N(CH₃)PCl₂NPCl₂N(CH₃)) 
• 593-51-1 methylamine hydrochloride 
• 10294-34-5 boron trichloride 
• 97923-85-8 dichloroboranyl-methyl-amine 
• 557-66-4 ethanamine hydrochloride 
• 4459-06-7 methyldisilylamine 
• 920-68-3 heptamethyldisilazane 

Downstream Products

• 16872-09-6 1,2-dicarba-closo-dodecaborane⁽¹²⁾ 
• 23550-71-2 N-trimethyl-B-tris(pentadeuterophenyl)borazine 
• 33911-15-8 N-Trimethyl-B-tricyclopentadienyl-borazol 
• 22871-80-3 N-trimethyl-B-tris(triphenylgermyl)borazine 
• 126583-47-9 (p-vinylphenyl)(diphenyl)(1,3,5-trimethyl)borazine 
• 126583-46-8 (allyl)(diphenyl)(1,3,5-trimethyl)borazine 
• 909-21-7 1,3,5-Trimethyl-2,4,6-triphenyl-borazin 
• 126583-45-7 (vinyl)(diphenyl)(1,3,5-trimethyl)borazine 
• 5562-82-3 2,4,6-Tris-(2,6-dimethyl-phenyl)-1,3,5-trimethyl-[1,3,5,2,4,6]triazatriborinane 
• 5122-92-9 1,3,5-Trimethyl-2,4,6-tris-(2,4,6-trimethyl-phenyl)-[1,3,5,2,4,6]triazatriborinane 
• 5572-93-0 (B(4-CH₃CO-2,6-(CH₃)2-C₆H₂)NCH₃)3 
• 2723-57-1 N-trimethyl-B-tris(pentafluorophenyl)borazine 
• 126583-44-6 (p-vinylphenyl)(pentamethyl)borazine 
• 877-07-6 hexamethylborazine 

Relevant articles and documents

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Alkylborazine compound and production method for the same

In the process of synthesizing alkylborazine compound represented by the chemical formula 2, by a reaction of a halogenated borazine compound represented by the chemical formula 1 with a Grignard reagent, thus synthesized alkylborazine compound is washed with water, or subjected to sublimation purification or distillation purification at least three times, and/or subjected to distillation purification at least twice. In the formulas, R1 independently represents alkyl group; R2 independently represents alkyl group; and X represents halogen atom.

Synthesis and thermal decomposition studies of some novel dimethyl(phenyl)silyl-substituted aminoboranes

Reactions of chloro(dimethyl)phenylsilane with primary amines have been used to obtain a series of compounds having the general formula C6H5(CH3)2SiNHR. The anions of those species are readily prepared, and may be reacted with trichloroborane or dichlorophenylborane to give the corresponding silylaminoboranes, C6H5(CH3)2SiN(R)B(X)Cl (X = Cl, Ph). The thermal properties of these silylaminoboranes have been probed using thermogravimetric analysis. The first step in their thermal degradation involves elimination of C6H5(CH3)2SiCl.