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922495-41-8

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922495-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 922495-41-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,2,4,9 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 922495-41:
(8*9)+(7*2)+(6*2)+(5*4)+(4*9)+(3*5)+(2*4)+(1*1)=178
178 % 10 = 8
So 922495-41-8 is a valid CAS Registry Number.

922495-41-8SDS

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 4-(2H-tetrazol-5-yl)phenyl-di(4-tolyl)amine

1.2 Other means of identification

Product number -
Other names -

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:922495-41-8 SDS

922495-41-8Relevant articles and documents

Light-emitting dyes derived from bifunctional chromophores of diarylamine and oxadiazole: Synthesis, crystal structure, photophysics and electroluminescence

He, Ze,Kan, Chi-Wai,Ho, Cheuk-Lam,Wong, Wai-Yeung,Chui, Chung-Hin,Tong, Ka-Lap,So, Shu-Kong,Lee, Tik-Ho,Leung, Louis M.,Lin, Zhenyang

, p. 333 - 343 (2011/06/21)

The synthesis, structural, photophysical, electrochemical and electroluminescent properties of a novel class of bifunctional molecule are reported in which the hole-transporting triarylamine and electron-transporting oxadiazole components were combined. The strongly luminescent compounds displayed good thermal and morphological stability as well as intense fluorescence both in solution and thin film at room temperature. The effects of the introduction of substituents with different electronic properties upon their absorption and emissive characteristics were correlated with theoretical calculations using density functional theory computations. The photophysics and electrochemistry of such systems were compared to those for the corresponding molecule without an oxadiazole ring. The bipolar compounds could be vacuum-sublimed and applied as emissive dopants for the fabrication of electrofluorescent, organic light-emitting devices with relatively simpler device structures, which can emit tunable colors by varying the aryl ring substituents.

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