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N-phenyl-5-pyridin-3-yl-1,3,4-oxadiazol-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54584-54-2

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54584-54-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54584-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,8 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54584-54:
(7*5)+(6*4)+(5*5)+(4*8)+(3*4)+(2*5)+(1*4)=142
142 % 10 = 2
So 54584-54-2 is a valid CAS Registry Number.

54584-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenyl-5-pyridin-3-yl-1,3,4-oxadiazol-2-amine

1.2 Other means of identification

Product number -
Other names N-Phenyl-5-(3-pyridinyl)-1,3,4-oxadiazol-2-amine

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:54584-54-2 SDS

54584-54-2Downstream Products

54584-54-2Relevant academic research and scientific papers

Novel 1,3,4-oxadiazole motifs bearing a quinoline nucleus: Synthesis, characterization and biological evaluation of their antimicrobial, antitubercular, antimalarial and cytotoxic activities

Ladani, Gaurav G.,Patel, Manish P.

, p. 9848 - 9857 (2015)

A series of quinoline based 1,3,4-oxadiazole derivatives (8a-l) were synthesized by a chloro-amine coupling reaction approach with different catalysts and solvents. Substituted 1,3,4-oxadiazole intermediates 7a-c were obtained from 2-substituted-N-phenylh

Hypervalent iodine(V) mediated mild and convenient synthesis of substituted 2-amino-1,3,4-oxadiazoles

Prabhu, Girish,Sureshbabu

, p. 4232 - 4234 (2012/09/07)

A simple protocol for the synthesis of 2-amino-1,3,4-oxadiazoles starting from the corresponding acylhydrazides by cyclodesulfurization of intermediate acylthiosemicarbazides mediated by o-iodoxybenzoic acid in good yields has been described. The protocol

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