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

89060-81-1

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89060-81-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89060-81-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,6 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89060-81:
(7*8)+(6*9)+(5*0)+(4*6)+(3*0)+(2*8)+(1*1)=151
151 % 10 = 1
So 89060-81-1 is a valid CAS Registry Number.

89060-81-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-nitrophenyl)-3-phenyl-1,2,4-triazole

1.2 Other means of identification

Product number -
Other names 1H-1,2,4-Triazole,1-(4-nitrophenyl)-3-phenyl

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:89060-81-1 SDS

89060-81-1Downstream Products

89060-81-1Relevant academic research and scientific papers

Metal-free Decarboxylative Annulation of 2-Aryl-2-isocyano-acetates with Aryldiazonium Salts: General Access to 1,3-Diaryl-1,2,4-triazoles

Tian, Yu-Ting,Zhang, Fa-Guang,Nie, Jing,Cheung, Chi Wai,Ma, Jun-An

supporting information, p. 227 - 233 (2020/10/12)

Isocyanoacetates are versatile substrates for the synthesis of heterocyclic compounds, but the concomitant decarboxylation remains rare. Herein we report a decarboxylative annulation reaction of 2-aryl-2-isocyanoacetates with aryldiazonium salts. This metal-free, base-promoted protocol allows for the access to a broad collection of 1,3-diaryl-1,2,4-triazoles, including chiral triazole-based binaphthalene ligands, drug mimics, and synthetic intermediates of druglike molecules. (Figure presented.).

An approach to 1-aryl-1,2,4-triazoles

Buzykin,Bredikhina

, p. 59 - 61 (2007/10/02)

A series of different 1,3,5-trisubstituted 1,2,4-triazoles 9 have been readily prepared by simple oxidation of corresponding N-alkylamide arylhydrazones (amidrazones) 5 with hydrogen peroxide or potassium permanganate.

REACTION OF BENZONITRILE N-(p-NITROPHENYL)IMIDE WITH 5-SUBSTITUTED TETRAZOLES: A NEW ROUTE TO SUBSTITUTED 1,2,4-TRIAZOLES VIA N-HYDRAZONOYLTETRAZOLES

Butler, Richard N.,Fitzgerald, Kevin J.

, p. 1587 - 1592 (2007/10/02)

A wide range of phenyl 5-R-substituted (R = aryl, alkyl, amino, halo, H) 1- and 2-hydrazonoyltetrazoles has been synthesized.Substituent effects on the orientation of nitrile imide attack on 5-aryltetrazoles are reported.Thermolysis and fragmentation of t

About Nitrile-Formamide-Chloride-Adducts. IX - Synthesis of 1,3- or 1,5-Disubstituted 1,2,4-Triazoles by the Reaction of Nitrile-Formamide Chloride-Adducts and their Products of Hydrolysis with Hydrazines

Liebscher, Juergen,Rumler, Andrea

, p. 311 - 319 (2007/10/02)

2-Aza-3-chloro-2-propeniminium salts 5, which are easily available by the addition of formamide chlorides 1 to nitriles 2 react smoothly with hydrazines 9 giving rise to 1,3-disubstituted 1,2,4-triazoles 11.When the 2-aza-3-chloro-2-propeniminium salts 5

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