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3,5-Bis(phenyl)-1,2,4-selenadiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65599-20-4

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65599-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65599-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,9 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65599-20:
(7*6)+(6*5)+(5*5)+(4*9)+(3*9)+(2*2)+(1*0)=164
164 % 10 = 4
So 65599-20-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H10N2Se/c1-3-7-11(8-4-1)13-15-14(17-16-13)12-9-5-2-6-10-12/h1-10H

65599-20-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-diphenyl-1,2,4-selenadiazole

1.2 Other means of identification

Product number -
Other names 1,2,4-Selenadiazole,3,5-diphenyl

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:65599-20-4 SDS

65599-20-4Relevant academic research and scientific papers

Straightforward and Expeditious One-Pot Tandem Synthesis of 3,5-Diaryl-1,2,4-Selenadiazoles from Aryl Nitriles

Almansaf, Zainab,Beyzavi, M. Hassan,Khosropour, Ahmad R.,Majnooni, Sahar,Tsuji, Miu,Zali-Boeini, Hassan

, p. 4279 - 4283 (2019/11/14)

A one-pot process for the efficient synthesis of 3,5-diaryl-1,2,4-selenadiazoles from aryl nitriles has been developed. This tandem transformation was performed in excellent yields (91-98percent) via in situ selenoamidation and a subsequent oxidative dime

Selenium heterocycles. XLIII. Syntheses of 3,5-diaryl-1,2,4- thiadiazoles and 3,5-diaryl-1,2,4-selenadiazoles

Shafiee,Ebrahimzadeh,Maleki

, p. 901 - 903 (2007/10/03)

Starting from readily available α-arylsulfonyl-α- bromoacetophenones 2 a series of 3,5-diaryl-1,2,4-thiadiazoles and 3,5-diaryl-1,2,4-selenadiazoles were prepared in moderate yield. Reaction of compounds 2 with thiourea or selenourea gave 2-amino-5-arylsu

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