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10480-11-2

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10480-11-2 Usage

General Description

1-(4-nitrophenyl)-5-phenyl-4,5-dihydrotriazole is a chemical compound with the molecular formula C15H12N4O2. It is a triazole derivative that contains a nitrophenyl group and a phenyl group. 1-(4-nitrophenyl)-5-phenyl-4,5-dihydrotriazole is often used in research and pharmaceutical applications, particularly in the development of new drugs and organic synthesis. It may also have potential applications in the field of agricultural chemicals and materials science. The specific properties and potential uses of this compound are still being investigated and explored.

Check Digit Verification of cas no

The CAS Registry Mumber 10480-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,8 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10480-11:
(7*1)+(6*0)+(5*4)+(4*8)+(3*0)+(2*1)+(1*1)=62
62 % 10 = 2
So 10480-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N4O2/c19-18(20)13-8-6-12(7-9-13)17-14(10-15-16-17)11-4-2-1-3-5-11/h1-9,14H,10H2

10480-11-2SDS

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 1-(4-nitrophenyl)-5-phenyl-4,5-dihydrotriazole

1.2 Other means of identification

Product number -
Other names 1-(4-nitrophenyl)-5-phenyl-4,5-dihydro-1h-1,2,3-triazole

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:10480-11-2 SDS

10480-11-2Relevant articles and documents

Metal-Free 1,2,3-Triazole Synthesis in Deep Eutectic Solvents

Díez-González, Silvia,Haselgrove, Samuel,Sebest, Filip,White, Andrew J. P.

supporting information, p. 605 - 609 (2020/04/08)

The metal-free regioselective preparation of 1,5- and 1,4-disubstituted triazoles is reported through a cycloaddition-elimination sequence. Reactions were carried out in environmentally friendly deep eutectic solvent (DES) and pure products were isolated

Triazolines. XXXIX. 1,5-Diaryl-δ2-1,2,3-triazolines as Aphicides: Mechanism of Action via Aziridine Formation

Kadaba, Pankaja K.

, p. 299 - 304 (2007/10/03)

The aphicidal activity of 21 different 1,5-diphenyl-Δ2-1,2,3-triazolines, conveniently prepared utilizing the catalytic effect of water on the 1,3-cycloaddition of diazomethane to Shiff bases in aqueous dioxane, was evaluated. Triazolines beari

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