115299-08-6 Usage
Description
2-(3-METHOXY-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is a highly specific chemical compound belonging to the Thiazoles class. It features a unique structure with an ethyl ester group attached to a thiazole carboxylic acid, which is further linked to a methoxy-substituted phenyl group. Thiazoles are organosulfur compounds characterized by a five-membered C3NS ring. Although there is limited information available on the specific properties, uses, or safety of this exact compound, it may be utilized in various research and development activities within scientific laboratories.
Uses
Used in Pharmaceutical Research and Development:
2-(3-METHOXY-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is used as a research compound for exploring its potential applications in the pharmaceutical industry. Its unique structure and properties may offer new avenues for drug discovery and development, particularly in the areas of medicinal chemistry and drug design.
Used in Chemical Synthesis:
In the field of organic chemistry, 2-(3-METHOXY-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is used as a synthetic intermediate for the preparation of various complex organic molecules. Its unique functional groups and structural features make it a valuable building block for the synthesis of novel compounds with potential applications in various industries.
Used in Material Science:
2-(3-METHOXY-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER may also find applications in material science, particularly in the development of new materials with unique properties. Its organosulfur nature and the presence of the thiazole ring could contribute to the creation of materials with enhanced stability, reactivity, or other desirable characteristics.
Used in Analytical Chemistry:
In analytical chemistry, 2-(3-METHOXY-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER can be employed as a reference compound or a standard for the development and validation of analytical methods. Its specific structure and properties may be useful for calibrating instruments, testing methodologies, or comparing results in various analytical techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 115299-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,2,9 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 115299-08:
(8*1)+(7*1)+(6*5)+(5*2)+(4*9)+(3*9)+(2*0)+(1*8)=126
126 % 10 = 6
So 115299-08-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO3S/c1-3-17-13(15)11-8-18-12(14-11)9-5-4-6-10(7-9)16-2/h4-8H,3H2,1-2H3
115299-08-6Relevant articles and documents
I2/TBHP-Mediated tandem cyclization and oxidation reaction: Facile access to 2-substituted thiazoles and benzothiazoles
Liu, Li,Tan, Chen,Fan, Rong,Wang, Zihan,Du, Hongguang,Xu, Kun,Tan, Jiajing
, p. 252 - 256 (2019)
The efficient synthesis of 2-substituted thiazoles and benzothiazoles has been accomplished employing readily available cysteine esters and 2-aminobenzenethiols as N and S sources. The reaction proceeds under an I2/TBHP system and involves a on
