5562-53-8

Basic information

• Product Name: (5Z)-5-(3-hydroxybenzylidene)-2-(morpholin-4-yl)-1,3-thiazol-4(5H)-one
• Synonyms: (5Z)-5-(3-Hydroxybenzylidene)-2-(morpholin-4-yl)-1,3-thiazol-4(5H)-one; 4(5H)-Thiazolone, 5-[(3-hydroxyphenyl)methylene]-2-(4-morpholinyl)-, (5Z)-; 5-(3-Hydroxy-benzylidene)-2-morpholin-4-yl-thiazol-4-one
• CAS NO: 5562-53-8
• Molecular Formula: C₁₄H₁₄N₂O₃S
• Molecular Weight: 290.3376
• Mol File: 5562-53-8.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 505.9°C at 760 mmHg
• Flash Point: 259.7°C
• Density: 1.42g/cm³
• Vapor Pressure: 7.42E-11mmHg at 25°C
• Refractive Index: 1.684
• CAS DataBase Reference: (5Z)-5-(3-hydroxybenzylidene)-2-(morpholin-4-yl)-1,3-thiazol-4(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (5Z)-5-(3-hydroxybenzylidene)-2-(morpholin-4-yl)-1,3-thiazol-4(5H)-one(5562-53-8)
• EPA Substance Registry System: (5Z)-5-(3-hydroxybenzylidene)-2-(morpholin-4-yl)-1,3-thiazol-4(5H)-one(5562-53-8)

Safety Data

• Hazardous Substances Data: 5562-53-8(Hazardous Substances Data)

Usage

Description

(5Z)-5-(3-hydroxybenzylidene)-2-(morpholin-4-yl)-1,3-thiazol-4(5H)-one is a thiazole derivative characterized by a molecular structure that features a thiazole ring and a morpholine moiety. This heterocyclic compound possesses potential biological activity, with its (5Z) stereochemistry denoting a specific atomic arrangement around a double bond. (5Z)-5-(3-hydroxybenzylidene)-2-(morpholin-4-yl)-1,3-thiazol-4(5H)-one also includes a 3-hydroxybenzylidene group, indicating the presence of a hydroxyl group attached to a benzylidene moiety. These functional groups endow the compound with the capacity for diverse chemical and biological interactions, positioning it as a potential building block for synthesizing other related compounds with pharmacological properties.

Uses

Used in Pharmaceutical Industry:
(5Z)-5-(3-hydroxybenzylidene)-2-(morpholin-4-yl)-1,3-thiazol-4(5H)-one is used as a precursor in the synthesis of pharmaceutical compounds for its potential biological activity and the presence of functional groups that facilitate chemical modifications and interactions with biological targets.
Used in Chemical Research:
In the field of chemical research, (5Z)-5-(3-hydroxybenzylidene)-2-(morpholin-4-yl)-1,3-thiazol-4(5H)-one serves as a model compound for studying the properties and reactivity of thiazole derivatives, as well as exploring the effects of stereochemistry on molecular behavior.
Used in Drug Development:
(5Z)-5-(3-hydroxybenzylidene)-2-(morpholin-4-yl)-1,3-thiazol-4(5H)-one is utilized in drug development as a lead compound for the discovery of new therapeutic agents, given its structural features that may confer pharmacological properties and its potential for further chemical modification to optimize activity and selectivity.