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5-(4-tert-butylphenyl)-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.

506407-84-7

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506407-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 506407-84-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,6,4,0 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 506407-84:
(8*5)+(7*0)+(6*6)+(5*4)+(4*0)+(3*7)+(2*8)+(1*4)=137
137 % 10 = 7
So 506407-84-7 is a valid CAS Registry Number.

506407-84-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-amine

1.2 Other means of identification

Product number -
Other names F2145-0168

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:506407-84-7 SDS

506407-84-7Relevant academic research and scientific papers

Photocatalytic oxidative heterocyclization of semicarbazones: An efficient approach for the synthesis of 1,3,4-oxadiazoles

Kapoorr, Ritu,Singh, Sachchida N.,Tripathi, Shubhangi,Yadav, Lal Dhar S.

supporting information, p. 1201 - 1206 (2015/06/02)

Abstract A highly efficient eosin Y catalyzed oxidative heterocyclization of semicarbazones was established under visible-light photoredox catalysis using CBr4 as a bromine source. The protocol renders a rapid, mild, and efficient access to val

A convenient synthesis of 5-substituted 2-amino-1,3,4-oxadiazoles from corresponding acylthiosemicarbazides using iodine and Oxone

Shinde, Vikas N.,Ugarkar, Bheemarao G.,Ghorpade, Sandeep R.

, p. 53 - 54 (2013/04/10)

A convenient methodology has been developed for the synthesis of substituted 2-amino-1,3,4-oxadiazoles from corresponding acylthiosemicarbazides using catalytic amount of iodine/KI in the presence of Oxone as a bulk oxidant. This offers the adv

SMALL MOLECULE MODULATORS OF CELL ADHESION

-

Page/Page column 39, (2009/12/05)

Compounds, particularly compounds having activity as modulators of cadherin-mediated cell adhesion having the following structure: or a pharmaceutically acceptable salt, stereoisomer or prodrug thereof, wherein R1, R2, R3,

N,N-dialkyl-N′-chlorosulfonylchloroformamidines in heterocyclic synthesis. II. Thiazolo-, thiadiazolo-, and oxadiazolo-fused [1,2,4,6]thiatriazine dioxides

Fallon, Gary D.,Francis, Craig L.,Johansson, Katarina,Liepa, Andris J.,Woodgate, Ruth C. J.

, p. 891 - 900 (2007/10/03)

N,N-dialkyl-N′-chlorosulfonylchloroformamidines 1 were treated with 2-aminothiazoline, 2-aminothiazoles, 2-aminobenzothiazoles, 2-amino-1,3,4- thiadiazoles, and 2-amino-1,3,4-oxadiazoles to give a 6,7-dihydrothiazolo[3,2-b] [1,2,4,6]thiatriazine dioxide 3

Oxidation of 2-amino-5-aryl-1,3,4-oxadiazole by sodium periodate: A kinetic study

Pradhan, Banasova,Misro,Padhy, Arun Kumar

, p. 898 - 900 (2007/10/03)

Kinetics of oxidation of a few 2-amino-5-aryl-1,3,4-oxadiazoles by sodium periodate in aqueous acetic acid-HClO4 medium have been studied. The reaction follows a first order rate each with respect to oxidant and substrate concentration. A suita

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