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62507-51-1

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62507-51-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62507-51-1 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 62507-51:
(7*6)+(6*2)+(5*5)+(4*0)+(3*7)+(2*5)+(1*1)=111
111 % 10 = 1
So 62507-51-1 is a valid CAS Registry Number.

62507-51-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxyphenyl)-5-(4-nitrophenyl)-1,3,4-oxadiazole

1.2 Other means of identification

Product number -
Other names 2-<4-Nitro-phenyl>-5-<4-methoxy-phenyl>-1,3,4-oxadiazol

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:62507-51-1 SDS

62507-51-1Relevant articles and documents

C-H arylation of azaheterocycles: A direct ligand-free and Cu-catalyzed approach using diaryliodonium salts

Kumar, Dalip,Pilania, Meenakshi,Arun,Pooniya, Savita

supporting information, p. 6340 - 6344 (2014/08/18)

An efficient and high yielding Cu-catalyzed direct C-H arylation of azaheterocycles including oxadiazoles, thiadiazoles, benzoxazoles and benzothiazoles has been achieved by employing easily accessible diaryliodonium salts. the Partner Organisations 2014.

Convenient preparation of unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles promoted by Dess-Martin reagent

Dobrotǎ, Cristian,Paraschivescu, Codru?a C.,Dumitru, Ioana,Matache, Mihaela,Baciu, Ion,Ru?ǎ, Lavinia L.

scheme or table, p. 1886 - 1888 (2009/07/05)

2,5-Disubstituted 1,3,4-oxadiazoles have been conveniently prepared by oxidative cyclization of N-acyl-N′-aryliden-hydrazines promoted by an excess of Dess-Martin periodinane under mild conditions (23 examples, up to 92% isolated yields).

An expeditious and convenient one pot synthesis of 2,5-disubstituted-1,3,4-oxadiazoles

Mashraqui, Sabir H.,Ghadigaonkar, Shailesh G.,Kenny, Rajesh S.

, p. 2541 - 2545 (2007/10/03)

A convenient, one pot procedure is reported for the synthesis of a variety of 2,5-disubstituted-1,3,4-oxadiazoles by condensing monoarylhydrazides with acid chlorides in HMPA solvent under the microwave heating. The yields are good to excellent, the process is rapid and does not need any added acid catalyst or dehydrating reagent.

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