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20069-34-5

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20069-34-5 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 8 carbon atoms, 6 hydrogen atoms, 2 nitrogen atoms, and 1 sulfur atom.
2. Heterocyclic organic compound

Explanation

A heterocyclic compound is a cyclic compound containing atoms of at least two different elements. In this case, the compound has a five-membered ring consisting of carbon, nitrogen, and sulfur atoms.
3. Five-membered ring structure

Explanation

The compound has a ring structure with five atoms, which are connected in a closed loop.

Explanation

The five-membered ring of the compound is made up of three carbon atoms, one nitrogen atom, and one sulfur atom.
5. Phenyl group at the 3-position

Explanation

A phenyl group (C6H5) is attached to the 3rd position of the thiadiazole ring, which influences the compound's chemical and physical properties.

Explanation

The compound has potential uses in the pharmaceutical industry due to its antimicrobial, antifungal, and antiviral activities.
7. Antimicrobial activity

Explanation

The compound exhibits the ability to inhibit or kill microorganisms, making it useful in the development of antimicrobial drugs.
8. Antifungal activity

Explanation

The compound demonstrates the ability to inhibit or destroy fungi, which can be useful in the development of antifungal medications.
9. Antiviral activity

Explanation

The compound shows the potential to inhibit or inactivate viruses, which can be applied in the development of antiviral drugs.

Explanation

The compound is being studied for its potential use as a starting material in the synthesis of various pharmaceutical and agricultural chemicals, due to its unique chemical structure and properties.

Composition

Three carbon atoms, one nitrogen atom, and one sulfur atom

Potential applications

Pharmaceutical industry

Precursor in synthesis

Pharmaceutical and agricultural chemicals

Check Digit Verification of cas no

The CAS Registry Mumber 20069-34-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,6 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20069-34:
(7*2)+(6*0)+(5*0)+(4*6)+(3*9)+(2*3)+(1*4)=75
75 % 10 = 5
So 20069-34-5 is a valid CAS Registry Number.

20069-34-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-2H-1,2,4-thiadiazole-5-thione

1.2 Other means of identification

Product number -
Other names 3-phenyl-1,2,4-thiadiazole-5-thiol

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:20069-34-5 SDS

20069-34-5Relevant articles and documents

Synthesis of 3,5-disubstituted-5,6-dihydro-4h-1,2,5-oxadiazine-6-thiones 1 and 3,5-disubstituted-1,2,4-thiadiazoles

Agirbas, Hikmet,Dueruest, Yasar,Karahasanoglu, Aysun

, p. 173 - 178 (2007/10/03)

3,5-Disubstituted-5,6-dihydro-4H-1,2,5-oxadiazine-6-thiones are prepared by the reaction of acetophenone oximes with thiophosgene. The thermal rearrangement of 3-phenyl-5-(p-tolyl)-5,6-dihydro-4H-1,2,5-oxadiazine-6-thione yields the corresponding 1,2,5-th

1,3-Dipolar Cycloaddition Reactions of Nitrilium Betaines with Aryl Thiocyanates and Selenocyanates

Greig, Derek J.,Hamilton, Douglas G.,McPherson, Michael,Paton, R. Michael,Crosby, John

, p. 607 - 612 (2007/10/02)

The carbon-nitrogen triple bond of aryl thiocyanates acts as a dipolarophile in 1,3-dipolar cycloadditions.Reaction with nitrile oxides, nitrile sulphides, and benzonitrile N-phenylimide yields, respectively, 5-arylthio-1,2,4-oxadiazoles, -thidiazoles and -triazoles.Aryl selenocyanates behave similarly forming 5-arylseleno-1,2,4-oxadiazoles and -thiadiazoles from nitrile oxides and sulphides.Divergent pathways are followed by the reactions of secondary amines such as piperidine with 5-arylthio-1,2,4-oxadiazoles and -thidiazoles, the former yielding 5-piperidyl-1,2,4-oxadiazoles and the latter dihydro-1,2,4-thiadiazole-5-thiones.

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