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13703-88-3

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13703-88-3 Usage

General Description

B-TRIBROMOBORAZINE, also known as Tri(bromoboryl)boron, is a chemical compound composed of boron, bromine, and nitrogen. It is a highly reactive compound and is mainly used in organic synthesis and as a precursor to other boron-containing compounds. B-TRIBROMOBORAZINE has been studied for its potential applications in materials science, including as a flame retardant and in the development of polymers with specific properties. It is a colorless solid that is soluble in organic solvents and has a molecular weight of 262.59 g/mol. Due to its reactivity, B-TRIBROMOBORAZINE should be handled and stored with caution and in accordance with proper safety protocols.

Check Digit Verification of cas no

The CAS Registry Mumber 13703-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,0 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13703-88:
(7*1)+(6*3)+(5*7)+(4*0)+(3*3)+(2*8)+(1*8)=93
93 % 10 = 3
So 13703-88-3 is a valid CAS Registry Number.
InChI:InChI=1/B3Br3H3N3/c4-1-7-2(5)9-3(6)8-1/h7-9H

13703-88-3 Well-known Company Product Price

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  • Alfa Aesar

  • (43723)  B-Tribromoborazine, 96%   

  • 13703-88-3

  • 1g

  • 639.0CNY

  • Detail
  • Alfa Aesar

  • (43723)  B-Tribromoborazine, 96%   

  • 13703-88-3

  • 5g

  • 3195.0CNY

  • Detail

13703-88-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-tribromo-1,3,5,2,4,6-triazatriborinane

1.2 Other means of identification

Product number -
Other names B-Tribromborazol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13703-88-3 SDS

13703-88-3Relevant articles and documents

Vaporization and thermal decomposition of B,B',B''-tribromoborazine

Kazakov,Timoshkin

, p. 557 - 563 (2012/07/14)

Vapor pressure as a function of temperature above solid and liquid (BrBNH)3 and the thermody-namic parameters of (BrBNH)3 sublimation and vaporization have been determined using static tensimetry with membrane null-manometer. The thermal decomposition of tribromoborazine has been studied in the saturated and unsaturated vapor regions. Irreversible decomposition occurred at noticeable rates at temperatures higher than 343 K and was accompanied by HBr evolution. In the unsaturated vapor region, thermal decomposition has far lower rates than in the saturated vapor region because of diffusion limitations. The activation energy of condensed-phase thermal decomposition of B,B',B''-tribromoborazine is 65 ± 3 kJ/mol, and this value proves that tribromoborazine decomposition at low temperatures is not accompanied by opening of the boron-nitrogen cycle.

Preparation of unsymmetrically B-substituted borazines and characterization of tris(4,6-diethylborazin-2-yl)amine

Bai,Niedenzu,Serwatowska,Serwatowski

, p. 4631 - 4635 (2008/10/08)

Symmetrically substituted B,B′,B″-triorganylborazines, (RBNR′)3, react with an equimolar quantity of boron trihalide, BX3 (X = Cl, Br), to form B-monohaloborazines, XR2B2N3R3, as well as RBX2, and with 2 molar equiv of BX3 to form the B,B′-dihaloborazines, X2RB3N3R′3. The compounds are obtained in good yield and purity, and are easily converted to other unsymmetrically B-substituted borazines. The borazines X(CH3)2B3N3(CH3) 3 (X = SCH3, NH2, C4H9, N[Si(CH3)2]), X(C2H5)2B3N3H3 (X = Br, SCH3), Cl(C2H5)2B3N3(CH 3)3, X2(C2H5)2B3N 3H3 (X = Br, SCH3), Cl(C6H5)2B3N3H 3, and Cl2(C2H5)B3N3(CH 3)3 have been prepared and characterized. The compound (H2N)(C2H5)2B3N 3H3 could not be obtained in the pure state; instead, it slowly condenses (even at room temperature) with the formation of the bis(borazin-2-yl)amine HN[(C2H5)2B3N3H 3]2 and the tris(borazin-2-yl)amine N[(C2H5)2B3N3H 3]3. The borazine (H2N)(CH3)2B3N3(CH 3)3 condenses at temperatures from 250 to 270°C to give HN [(CH3)2B3N3(CH3) 3]2. Reaction of this bis(borazin-2-yl)amine with LiC4H9 yields (C4H9)(CH3)2B3N 3(CH3)3 and (NHLi)(CH3)2B3N3(CH 3)3; the latter then reacts with Cl(CH3)2B3N3(CH3) 3 to regenerate HN[(CH3)2B3N3(CH3) 3]2. The unsymmetricaliy N-substituted borazine (C2H5)3B3N3H 2[Si(CH3)3] has been isolated and characterized.

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