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1,3,4-Oxadiazole, 2-(4-methylphenyl)-5-(4-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62507-52-2

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62507-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62507-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62507-52:
(7*6)+(6*2)+(5*5)+(4*0)+(3*7)+(2*5)+(1*2)=112
112 % 10 = 2
So 62507-52-2 is a valid CAS Registry Number.

62507-52-2SDS

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 2-(4-methylphenyl)-5-(4-nitrophenyl)-1,3,4-oxadiazole

1.2 Other means of identification

Product number -
Other names 2-<4-Nitro-phenyl>-5-p-tolyl-1,3,4-oxdiazol

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:62507-52-2 SDS

62507-52-2Relevant academic research and scientific papers

17O NMR studies of substituted 1,3,4-oxadiazoles

Gierczyk, Blazej,Zalas, MacIej,Kazmierczak, Marcin,Grajewski, Jakub,Pankiewicz, Radoslaw,Wyrzykiewicz, Bozena

experimental part, p. 648 - 654 (2012/01/06)

Three series of substituted 1,3,4-oxadiazoles were studied by 17O NMR spectroscopy. Chemical shifts values were correlated with empirical Hammett parameters as well as calculated bond lengths and chemical shielding values.

Synthesis, anti-HIV, and antifungal activity of new benzensulfonamides bearing the 2,5-disubstituted-1,3,4-oxadiazole moiety

Zareef, Muhammad,Iqbal, Rashid,Al-Masoudi, Najim A.,Zaidi, Javid H.,Arfan, Muhammad,Shahzad, Sohail A.

, p. 281 - 298 (2007/10/03)

A series of novel chiral and achiral N-[1-(1,3,4-oxadiazol-2ylthio)alkyl]- 4-methyl/chloro/methoxybenzenesulfonamides 5a-l were prepared by the reaction of 4-(4-methyl, chloro, methoxyphenylsulfonamido)alkyl carboxylic acid hydrazides 4a-l with CS2 and KO

Synthesis and optical properties of copolymers containing electron transporting 1,3,4-oxadiazole pendant groups

Wang, Hui,Ryu, Jeong-Tak,Han, Yoon Soo,Hur, Youngjune,Park, Lee Soon,Song, Minhyeon,Kwon, Younghwan

, p. 109/[389]-118/[398] (2007/10/03)

Well-defined copolymer, P(3,6-EHCZ-alt-MPAOXD), containing a triarylamine and N-alkylcarbazole groups (as hole transport moieties with blue emission) in the main chain and a 1,3,4-oxadiazole pendant group (as an electron transporting moiety) was synthesiz

An efficient one pot synthesis of 1,3,4-oxadiazoles

Tandon,Chhor

, p. 1727 - 1732 (2007/10/03)

Various 1,3,4-oxadiazoles have been synthesized in excellent yields by BF3·Et2O promoted cyclodehydration of 1,2-diacyl and diaroyl hydrazines prepared in situ from corresponding acid chlorides and hydrazine.

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