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1,2,3,4-Thiatriazole, 5-phenoxy- is a chemical compound with the molecular formula C7H4N3OS. It is a heterocyclic compound, specifically a thiatriazole derivative, which features a five-membered ring containing three nitrogen atoms and one sulfur atom. The phenoxy group is attached to the thiatriazole ring, providing a phenyl ring connected to an oxygen atom. 1,2,3,4-Thiatriazole, 5-phenoxy- is known for its potential applications in various chemical and pharmaceutical industries, such as in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Due to its unique structure and properties, it can be used as a building block or intermediate in the development of new molecules with specific therapeutic or chemical properties.

3549-20-0

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3549-20-0 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, 1,2,3,4-Thiatriazole, 5-phenoxyhas 9 carbon (C), 7 hydrogen (H), 3 nitrogen (N), 3 oxygen (O), and 1 sulfur (S) atoms.

Explanation

Thiatriazole is a family of heterocyclic organic compounds that contain a thiatriazole ring. 1,2,3,4-Thiatriazole, 5-phenoxyis a member of this family.

Explanation

A heterocyclic organic molecule is a ring-shaped molecule containing atoms of different elements. In this case, 1,2,3,4-Thiatriazole, 5-phenoxycontains nitrogen and sulfur atoms in its thiatriazole ring.

Explanation

The phenyl group (C6H5) is attached to the 5th position of the thiatriazole ring, which is one of the nitrogen atoms in the ring.

Explanation

Research has been conducted to explore the compound's potential effects on living organisms, particularly its ability to inhibit the growth of fungi and bacteria.

Explanation

Due to its potential antifungal and antimicrobial properties, 1,2,3,4-Thiatriazole, 5-phenoxyhas been considered for use in agriculture to control pests and weeds.

Explanation

More studies are required to gain a comprehensive understanding of the compound's properties, its effectiveness in various applications, and any potential side effects or limitations.

Family

Thiatriazole

Heterocyclic Organic Molecule

Nitrogen and Sulfur-containing

Phenyl Group Attachment

5-position of the thiatriazole ring

Biological and Pharmacological Properties

Studied for potential antifungal and antimicrobial activities

Agricultural Applications

Investigated as a pesticide or herbicide

Further Research

Needed to fully understand properties and potential uses

Check Digit Verification of cas no

The CAS Registry Mumber 3549-20-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,4 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3549-20:
(6*3)+(5*5)+(4*4)+(3*9)+(2*2)+(1*0)=90
90 % 10 = 0
So 3549-20-0 is a valid CAS Registry Number.

3549-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenyloxy-1,2,3,4-thiatriazole

1.2 Other means of identification

Product number -
Other names 5-Phenoxy-1,2,3,4-thiatriazol

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:3549-20-0 SDS

3549-20-0Relevant academic research and scientific papers

Episulfidation of strained cycloalkenes in the thermolysis of 5-aryloxy-1,2,3,4-thiatriazoles

Adam, Waldemar,Bargon

, p. 1959 - 1962 (2007/10/03)

The thermolysis of 5-aryloxythiatriazoles 1 in the presence of norbornene (2a) and trans-cyclooctene (trans-2b) affords the corresponding thiiranes 3a and trans-3b in moderate yields. First-order kinetics are observed, suggesting that a sulfur intermediate, presumably dinitrogen sulfide, is generated in the fragmentation process of 1, which then serves as the active sulfur atom donor.

Red and infrared films containing either 5-thio-1,2,3,4-thiatriazoles and 5-oxy-1,2,3,4-thiatriazoles or 5-substituted-thio-1,2,3,4-thiatriazoles and 5-substituted-oxy-1,2,3,4-thiatriazoles

-

, (2008/06/13)

5-substituted-thio-1,2,3,4-thiatriazoles and 5-substituted-oxy-1,2,3,4-thiatriazoles have been found to be supersensitizers for silver halide photographic emulsions spectrally sensitized to the red and infrared regions of the electromagnetic spectrum.

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