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51039-49-7

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51039-49-7 Usage

Chemical Properties

Pale yellow solid

Check Digit Verification of cas no

The CAS Registry Mumber 51039-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,3 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51039-49:
(7*5)+(6*1)+(5*0)+(4*3)+(3*9)+(2*4)+(1*9)=97
97 % 10 = 7
So 51039-49-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3/c1-2-4-8(5-3-1)11-9-6-7-10-11/h1-7H

51039-49-7SDS

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 2-phenyltriazole

1.2 Other means of identification

Product number -
Other names 2-Phenyl-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:51039-49-7 SDS

51039-49-7Relevant articles and documents

Optimization of the synthesis of 2-phenyl-1,2,3-triazole

Myachina,Ermakova,Kuznetsova,Sultangareev,Larina,Klyba,Suchanov,Trofimov

, p. 79 - 81 (2010)

The synthesis of 2-phenyl-1,2,3-triazole by the cyclization of glyoxal phenylosazone in high-boiling solvents in the presence of copper triflate catalyst has been optimized. The structure of the product was confirmed by data of IR, 1H, 13C, and 15N NMR spectroscopy, mass spectrometry, and elemental analysis.

Sensitive Energetics from the N-Amination of 4-Nitro-1,2,3-Triazole

Wozniak, Dominique R.,Salfer, Benjamin,Zeller, Matthias,Byrd, Edward F. C.,Piercey, Davin G.

, p. 806 - 811 (2020/05/25)

Energetic N-amino-C-nitro compounds 1-amino-4-nitro-1,2,3-triazole and 2-amino-4-nitro-1,2,3-triazole are characterized for the first time as energetic materials. These compounds were characterized chemically by nuclear magnetic resonance (NMR), Infrared

Molybdenum-Catalyzed Deoxygenation of Heteroaromatic N-Oxides and Hydroxides using Pinacol as Reducing Agent

Rubio-Presa, Rubén,Fernández-Rodríguez, Manuel A.,Pedrosa, María R.,Arnáiz, Francisco J.,Sanz, Roberto

, p. 1752 - 1757 (2017/05/22)

A molybdenum-catalyzed deoxygenation of pyridine N-oxides and N-hydroxybenzotriazoles, as well as other azole N-oxides, has been developed using pinacol as an environmentally friendly oxo-acceptor. The only by-products are acetone and water making the process a convenient alternative to established protocols in terms of waste generation. The reaction is highly chemoselective and a variety of functional groups are tolerated. The processes are usually very clean allowing the isolation of the pure deoxygenated products after a simple extraction in most cases. (Figure presented.).

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