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

52376-72-4

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52376-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52376-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,7 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52376-72:
(7*5)+(6*2)+(5*3)+(4*7)+(3*6)+(2*7)+(1*2)=124
124 % 10 = 4
So 52376-72-4 is a valid CAS Registry Number.

52376-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-nitrophenyl)selenadiazole

1.2 Other means of identification

Product number -
Other names 1,2,3-Selenadiazole,4-(3-nitrophenyl)

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:52376-72-4 SDS

52376-72-4Relevant academic research and scientific papers

Preparation of 2-Arylethynylselanylacetonitriles from 4-Aryl-1,2,3-selenadiazoles

O'Connor,Sachinvala,Ganjian

, p. 1167 - 1169 (2015/08/06)

Base decomposition of 4-(substituted phenyl)-1,2,3-selenadiazoles at room temperature resulted in 2-(substituted phenyl)-ethynylselenolate anions, which were immediately reacted with bromoacetonitrile to give a series of 2-(substituted phenyl)ethynylselan

A novel synthesis of benzo[ b ]selenophenes via regioselective intramolecular transformation of 4-(3-Nitroaryl)-1,2,3-selenadiazoles

Lyapunova, Anna G.,Petrov, Mikhail L.,Androsov, Dmitry A.

supporting information, p. 1744 - 1747 (2013/06/26)

Base-promoted transformation of 4-(3-nitroaryl)-1,2,3-selenadiazoles via intermediate formation of eneselenolates followed by 5-exo-trig cyclization is reported. The regiochemistry of the intramolecular cyclization is condition-dependent. In the presence

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