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

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

Downstream Products

• 909-21-7 1,3,5-Trimethyl-2,4,6-triphenyl-borazin 
• 1004-35-9 1,3,5-trimethyl-cyclotriborazane 
• 126583-46-8 (allyl)(diphenyl)(1,3,5-trimethyl)borazine 
• 16872-09-6 1,2-dicarba-closo-dodecaborane⁽¹²⁾ 
• 126583-44-6 (p-vinylphenyl)(pentamethyl)borazine 
• 877-07-6 hexamethylborazine 
• 97-94-9 triethyl borane 
• 715-62-8 B,B',B''-triethyl-N,N',N''-trimethylborazine 
• 2723-57-1 N-trimethyl-B-tris(pentafluorophenyl)borazine 
• 13722-15-1 1,3,5-trifluoro-2,4,6-trimethylborazine 
• 18825-49-5 B-Tris-triphenylsilyloxy-N-trimethyl-borazol 
• 18825-50-8 B-tris(triphenylsilyl)-N-trimethylborazine 
• 14606-27-0 1,3,5-Trimethyl-2,4,6-tris-pentafluorphenoxy-borazin 
• 14747-47-8 N-trimethyl-B-tris(pentafluorophenylamino)borazine 

Relevant articles and documents

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METHOD FOR PRODUCING TRICHLOROBORAZINE COMPOUND AND METHOD FOR PRODUCING ALYKYLBORAZINE COMPOUND

PROBLEM TO BE SOLVED: To provide a means for efficiently purifying a synthesized trichloroborazine compound. SOLUTION: The subject method for producing the trichloroborazine compound comprises the following steps. A step of reacting boron trichloride with an amine compound represented by R1NH3X (wherein, R1 is hydrogen atom or an alkyl group; and X is a halogen atom) in a solvent and producing the trichloroborazine compound represented by formula 2 (wherein, R2s may each the same or different and are each hydrogen atom or an alkyl group), a step of filtering the reaction solution and affording a filtrate and a step of distilling off the solvent from the filtrate and providing a solid substance composed of the trichloroborazine compound.

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.