886366-81-0 Usage
Description
4-(3-Methoxy-phenyl)-thiazole-2-carboxylic acid ethyl ester is a chemical compound characterized by the molecular formula C14H13NO3S. It is an ethyl ester derivative of thiazole-2-carboxylic acid, featuring a thiazole ring and a carboxylic acid group. Additionally, it incorporates a methoxyphenyl group attached to the thiazole ring, which may contribute to its potential applications in various fields.
Uses
Used in Organic Synthesis:
4-(3-Methoxy-phenyl)-thiazole-2-carboxylic acid ethyl ester serves as a valuable intermediate in organic synthesis, particularly for the preparation of complex organic molecules and pharmaceutical agents. Its unique structure allows it to participate in a range of chemical reactions, facilitating the synthesis of diverse organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-(3-Methoxy-phenyl)-thiazole-2-carboxylic acid ethyl ester is utilized as a building block for the development of new drugs. Its chemical properties and reactivity make it suitable for the creation of bioactive molecules with potential therapeutic applications.
Used in Pharmaceutical Research:
4-(3-Methoxy-phenyl)-thiazole-2-carboxylic acid ethyl ester is also employed in pharmaceutical research for the exploration of its potential as a therapeutic agent. Its specific properties and interactions with biological targets may lead to the discovery of new treatments for various diseases and conditions.
Used in Chemical Research:
4-(3-METHOXY-PHENYL)-THIAZOLE-2-CARBOXYLIC ACID ETHYL ESTER is utilized in chemical research to study its properties and reactivity. Understanding its behavior in different chemical environments can provide insights into the development of new synthetic methods and the creation of novel chemical entities.
Used in Material Science:
4-(3-Methoxy-phenyl)-thiazole-2-carboxylic acid ethyl ester may also find applications in material science, where its unique structural features could contribute to the development of new materials with specific properties, such as improved stability, reactivity, or selectivity in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 886366-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,3,6 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 886366-81:
(8*8)+(7*8)+(6*6)+(5*3)+(4*6)+(3*6)+(2*8)+(1*1)=230
230 % 10 = 0
So 886366-81-0 is a valid CAS Registry Number.
