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4-(5-Phenyl-1,3,4-thiadiazol-2-yl)pyridine is a chemical compound characterized by its unique molecular structure, which features a pyridine ring fused with a 1,3,4-thiadiazol ring. The 1,3,4-thiadiazol ring is substituted with a phenyl group at the 5-position, and the pyridine ring is located at the 4-position of the thiadiazole. 4-(5-Phenyl-1,3,4-thiadiazol-2-yl)pyridine is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its interesting electronic and chemical properties. It is often synthesized through chemical reactions involving pyridine and other precursors, and its structure can be confirmed through spectroscopic techniques such as NMR and mass spectrometry. The compound's specific applications and properties are under ongoing research, as scientists explore its potential in different areas of chemistry and technology.

4291-07-0

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4291-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4291-07-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,9 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4291-07:
(6*4)+(5*2)+(4*9)+(3*1)+(2*0)+(1*7)=80
80 % 10 = 0
So 4291-07-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H9N3S/c1-2-4-10(5-3-1)12-15-16-13(17-12)11-6-8-14-9-7-11/h1-9H

4291-07-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(5-Phenyl-1,3,4-thiadiazol-2-yl)pyridine

1.2 Other means of identification

Product number -
Other names 2-Phenyl-5-<4-vinyl-phenyl>-oxazol

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:4291-07-0 SDS

4291-07-0Downstream Products

4291-07-0Relevant academic research and scientific papers

Greener and rapid access to bio-active heterocycles: one-pot solvent-free synthesis of 1,3,4-oxadiazoles and 1,3,4-thiadiazoles

Polshettiwar, Vivek,Varma, Rajender S.

, p. 879 - 883 (2008/09/17)

A novel one-pot solvent-free synthesis of 1,3,4-oxadiazoles and 1,3,4-thiadiazoles by condensation of acid hydrazide and triethyl orthoalkanates under microwave irradiations is reported. This green protocol was catalyzed efficiently by solid supported NafionNR50 and phosphorus pentasulfide in alumina (P4S10/Al2O3) with excellent yields.

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