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1H-1,2,4,3-Triazaborole, 2,3-dihydro-2,3,5-triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77091-62-4

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77091-62-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77091-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,9 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77091-62:
(7*7)+(6*7)+(5*0)+(4*9)+(3*1)+(2*6)+(1*2)=144
144 % 10 = 4
So 77091-62-4 is a valid CAS Registry Number.

77091-62-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5-triphenyl-1H-1,2,4,3-triazaborole

1.2 Other means of identification

Product number -
Other names 1H-1,2,4,3-Triazaborole,2,3-dihydro-2,3,5-triphenyl

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:77091-62-4 SDS

77091-62-4Downstream Products

77091-62-4Relevant academic research and scientific papers

A Study of Boratriazaroles: An Underdeveloped Class of Heterocycles

Liew, Sean K.,Holownia, Aleksandra,Tilley, Andrew J.,Carrera, Elisa I.,Seferos, Dwight S.,Yudin, Andrei K.

, p. 10444 - 10453 (2016)

Boratriazaroles were discovered in the late 1960s, and since then, a variety of substituted boratriazarole derivatives have been prepared. However, no study has compared the properties of these BN heterocycles with their carbon-based analogues. In this work, we have prepared a series of boratriazarole derivatives and have investigated how structural variations in the five-member heterocycle affect photophysical and electronic properties. Boratriazaroles exhibit absorption and emission spectra comparable to those of their azacycle analogues but have a markedly lower quantum yield. The quantum yield can be increased with the incorporation of a 2-pyridyl substitution on the boratriazaroles, and the structural and optoelectronic properties are further influenced by the nature of the B-aryl substituent. Introducing an electron-deficient p-cyano group on the B-phenyl substituent creates a twisted intramolecular charge transfer state that causes a large Stokes shift and positive solvatochromism. Our work should serve to guide future synthetic efforts toward the application of boratriazaroles in materials science.

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