75820-45-0

Usage

Uses

Used in Pharmaceutical Research:
2(3H)-Thiazolone, 4-(1,1-dimethylethyl)is used as a building block for the development of new drugs, particularly in the fields of medicinal chemistry and drug discovery. Its unique structure and properties make it a valuable component in the synthesis of various pharmaceutical compounds.
Used in Organic Synthesis:
In the field of organic synthesis, 2(3H)-Thiazolone, 4-(1,1-dimethylethyl)serves as a key intermediate for the synthesis of complex organic molecules. Its reactivity and the presence of the tert-butyl group make it a useful precursor in the preparation of a wide range of chemical products.
Used in Antibacterial Applications:
2(3H)-Thiazolone, 4-(1,1-dimethylethyl)is used as an antibacterial agent due to its potential to inhibit the growth of various bacteria. Its chemical structure allows it to target specific bacterial enzymes or processes, making it a promising candidate for the development of new antibacterial drugs.
Used in Antifungal Applications:
Similarly, 2(3H)-Thiazolone, 4-(1,1-dimethylethyl)is also used as an antifungal agent, exhibiting potential to combat fungal infections. Its ability to interfere with fungal cell growth and reproduction makes it a valuable asset in the development of new antifungal medications.

Upstream product

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Relevant academic research and scientific papers

TETRAZOLINONE COMPOUNDS AND ITS USE

The present invention provides a compound having an excellent efficacy for controlling pests. A tetrazolinone compound of a formula (1): [wherein, R1 represents an C6-C16 aryl group, an C1-C12 alkyl group, a C3-C12 cycloalkyl group or an adamantyl group, etc., which each optionally be substituted; R2 represents a hydrogen atom, an C1-C12 alkyl group, or a halogen atom, etc.; R4 and R5 represent independently of each other a hydrogen atom or an C1-C3 alkyl group, etc.; R6, R7, R8 and R9 represent independently of each other a hydrogen atom, a halogen atom, an C1-C12 alkyl group, a C1-C12 haloalkyl group, an C2-C12 alkenyl group, a C3-C12 cycloalkyl group, an C1-C12 alkoxy group or a C1-C12 haloalkoxy group, etc.; X and Y represent independently of each other a sulfur atom or an oxygen atom; Q represents an oxygen atom or a sulfur atom; and R10 represents an C1-C6 alkyl group, etc.] shows an excellent controlling efficacy on pests.

The Structures of 4- and 5-Substituted Δ4-Thiazolin-2-ones

In order to establish the structures of compounds described as Δ4-thiazolin-2-ones ten sets of heterocycles (each comprising a 4- or 5-substituted Δ4-thiazolin-2-one, the N-methyl derivative, and the corresponding 2-methoxythiazole) have been examined by i.r., u.v., and 1H and 13C n.m.r. spectrometry.The i.r. results established that in solution the parent compounds exist entirely or predominantly as the 2-oxo-forms.This conclusion is supported by the 1H n.m.r. evidence, but the u.v. and 13C n.m.r. data do not give a clear distinction between the possible 2-oxo- and 2-hydroxy-structures.