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1,4,5-Triphenyl-4,5-dihydro-1H-tetrazaborole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20534-06-9

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20534-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20534-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,3 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20534-06:
(7*2)+(6*0)+(5*5)+(4*3)+(3*4)+(2*0)+(1*6)=69
69 % 10 = 9
So 20534-06-9 is a valid CAS Registry Number.

20534-06-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,5-triphenyltetrazaborole

1.2 Other means of identification

Product number -
Other names 1,4,5-Triphenyl-4,5-dihydro-1H-1,2,3,4,5-tetraazaborole

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:20534-06-9 SDS

20534-06-9Downstream Products

20534-06-9Relevant academic research and scientific papers

Boron Imides from the Thermal Decomposition of Diarylazidoboranes

Paetzold, Peter,Truppat, Ruediger

, p. 1531 - 1539 (2007/10/02)

Diarylazidoboranes Ar2BN3 (1a-d) are thermolyzed either into diazadiboretidines (ArBNAr)2 (2) or into borazines (ArBNAr)3 (3).After formation of only one half of the expected amount of N2, the boryltetrazaborolines 4c, d are isolated as intermediates.The boranes 1a-d are transformed into phenyltetrazaborolines 6a-d or into silyltetrazaborolines 7a-d by the action of phenyl or trimethylsilyl azide, respectively; the formation of 7b, d is accompanied by the formation of the open-chain aminoboranes 9b, d.The action of triethylborane on 1a-d yields the diborylamines 5a-d and, moreover, the diborylamines 8a, d, isomeric to 5a, d.The formation of boron imides ArB=NAr (10a-d) as reaction intermediates is discussed and, in favour of that, the reactions of 1c with O-N(Me)=CH-Ph, yielding 11c, and of 1a, d with B(sBu)3, yielding 5a', 8a', 5d', are referred too.

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