1011-41-2

Usage

Uses

Used in Organic Synthesis:
2-Morpholino-1,3-thiazole-5-carbaldehyde is used as a reagent in organic synthesis for the preparation of various heterocyclic compounds. Its unique structure allows for the creation of a wide range of chemical entities, making it a valuable component in the synthesis of pharmaceuticals and other organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Morpholino-1,3-thiazole-5-carbaldehyde is used as a starting material for the development of new drugs. Its potential pharmacological properties, such as its antifungal activity and its ability to inhibit protein kinases, make it a promising candidate for the treatment of various diseases and conditions.
Used as an Antifungal Agent:
2-Morpholino-1,3-thiazole-5-carbaldehyde is used as an antifungal agent due to its ability to inhibit the growth of fungi. This property makes it a valuable tool in the development of new antifungal medications, which can be used to treat a variety of fungal infections.
Used as a Protein Kinase Inhibitor:
2-Morpholino-1,3-thiazole-5-carbaldehyde is also used as an inhibitor of protein kinases, which are enzymes that play a crucial role in cellular signaling pathways. By inhibiting these enzymes, the compound can potentially be used to treat diseases that involve abnormal cell signaling, such as cancer.
Used in Biochemistry Research:
In biochemistry research, 2-Morpholino-1,3-thiazole-5-carbaldehyde has been studied for its potential application as a fluorescent tag for biomolecules. This allows researchers to track and study the behavior of these molecules in various biological systems, providing valuable insights into their functions and interactions.

InChI:InChI=1/C8H10N2O2S/c11-6-7-5-9-8(13-7)10-1-3-12-4-2-10/h5-6H,1-4H2

Upstream product

• 21429-06-1 2-(morpholine-1-yl)thiazole 
• 68-12-2 N,N-dimethyl-formamide 
• 3034-52-4 2-chlorothiazole 
• 4394-85-8 4-morpholinecarboxaldehyde 
• 110-91-8 morpholine 
• 95453-58-0 2-chloro-1,3-thiazole-5-carbaldehyde 

Relevant academic research and scientific papers

BENZOXAZOLE DERIVATIVES

It is intended to provide a benzoxazole derivative or a pharmaceutically acceptable salt or solvate thereof which is useful in the early diagnosis of a conformation disease; a composition or a kit containing the same for diagnosing a conformation disease; a medical composition for ttreating and/or preventing a conformation disease; and so on.

Triazolopyridine dyes and intermediates therefor

Triazolopyridine dyes of the formula STR1 where R1 is unsubstituted or substituted C1 -C20 -alkyl, unsubstituted or substituted phenyl, unsubstituted or substituted hydroxyl or unsubstituted or substituted mercapto, Q is a radical of the formula STR2 where R2 is a carbocyclic or heterocyclic radical, R3 is hydrogen or unsubstituted or substituted C1 -C4 -alkyl, R4 is hydrogen, unsubstituted or substituted C1 -C4 -alkyl or C1 -C4 -alkoxy, R5 is unsubstituted or substituted C1 -C8 -alkyl, unsubstituted or substituted phenyl, unsubstituted or substituted thienyl or unsubstituted or substituted C1 -C4 -alkoxy, or the radical CR3 R4 R5 together is C3 -C7 -cycloalkyl, C1 -C4 -haloalkyl, unsubstituted or substituted phenyl or unsubstituted or substituted thienyl, R6 is cyano, carbamoyl, carboxyl, C1 -C4 -alkoxycarbonyl or benzothiazolyl, and E is CH or nitrogen, and R7 is oxygen or a radical of an acidic--CH compound, a process for the thermal transfer of these dyes, their use for dyeing or printing synthetic materials and also triazolopyridines as intermediates for these dyes.

An Easy General Synthesis of 2-(N,N-Dialkylamino)thiazol-5-yl Aldehydes and Ketones

Reaction between 2-chloro-5-thiazolyl-lithium and N,N-dialkylformamides or amides gave 2-N,N-dialkylaminothiazol-5-yl aldehydes or ketones on quenching with water.Quenching with acid gave 2-chlorothiazole-5-yl aldehydes or ketones, from which chloride was easily displaced by free amines.