23012-30-8

Basic information

• Product Name: ETHYL 2,4-DIMETHYLOXAZOLE-5-CARBOXYLATE
• Synonyms: AKOS A0602-0415;ETHYL 2,4-DIMETHYLOXAZOLE-5-CARBOXYLATE;OTAVA-BB 7118560798;Ethyl 2,4-dimethyl-1,3-oxazole-5-carboxylate;2,4-dimethyl-5-oxazolecarboxylic acid ethyl ester;2,4-dimethyloxazole-5-carboxylic acid ethyl ester;2,4-DIMETHYLOXAZOLE-5-CARBOXYLATE;Ethyl 2,4-dimethyl-5-Oxazolecarboxylic acid
• CAS NO: 23012-30-8
• Molecular Formula: C₈H₁₁NO₃
• Molecular Weight: 169.18
• EINECS: 604-604-1
• Mol File: 23012-30-8.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 226.3°Cat760mmHg
• Flash Point: 90.6°C
• Appearance: /
• Density: 1.11g/cm³
• Vapor Pressure: 0.0826mmHg at 25°C
• Refractive Index: 1.472
• Storage Temp.: 2-8°C
• CAS DataBase Reference: ETHYL 2,4-DIMETHYLOXAZOLE-5-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 2,4-DIMETHYLOXAZOLE-5-CARBOXYLATE(23012-30-8)
• EPA Substance Registry System: ETHYL 2,4-DIMETHYLOXAZOLE-5-CARBOXYLATE(23012-30-8)

Safety Data

• Hazardous Substances Data: 23012-30-8(Hazardous Substances Data)

Usage

General Description

ETHYL 2,4-DIMETHYLOXAZOLE-5-CARBOXYLATE is a chemical compound with the molecular formula C8H11NO3. It is a ester derivative of 2,4-dimethyloxazole-5-carboxylic acid and is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is a colorless liquid with a fruity odor and is soluble in organic solvents. ETHYL 2,4-DIMETHYLOXAZOLE-5-CARBOXYLATE is known for its wide range of biological activities, including anti-inflammatory and antimicrobial properties. It is also used as a flavoring agent in the food industry. Overall, ETHYL 2,4-DIMETHYLOXAZOLE-5-CARBOXYLATE is a versatile chemical compound with various industrial and biological applications.

InChI:InChI=1/C8H11NO3/c1-4-11-8(10)7-5(2)9-6(3)12-7/h4H2,1-3H3

Upstream product

• 631-61-8 ammonium acetate 
• 64-19-7 acetic acid 
• 18632-42-3 2-acetoxy-acetoacetic acid ethyl ester 
• 638-07-3 ethyl (2-chloroaceto)acetate 
• 141-97-9 ethyl acetoacetate 
• 23652-67-7 ethyl (Z)-β-acetylaminobut-2-enoate 
• 60-35-5 acetamide 
• 609-15-4 ethyl 2-chloro-3-oxo-butyrate 

Downstream Products

• 214553-55-6 5-hydroxymethyl-2,4-dimethyloxazole 
• 69062-86-8 2,4-dimethyloxazole-5-carbaldehyde 
• 2510-37-4 2,4-dimethyl-oxazole-5-carboxylic acid 
• 885061-06-3 5-chloromethyl-2,4-dimethyloxazole 

Relevant articles and documents

Hypervalent iodane mediated reactions of: N -acetyl enamines for the synthesis of oxazoles and imidazoles

A hypervalent iodane reagent used for the intramolecular cyclization of N-acetyl enamines and intermolecular cyclocondensation of enamines and nitriles was investigated. The reaction was performed under mild conditions and gave oxazoles and imidazoles, respectively, in moderate to excellent yields. This transformation exhibits good reactivity, selectivity and functional group tolerance. The selectivity of the intra- or intermolecular reaction is dependent on the structure of N-acetyl enamines.

Synthesis of furanyl and oxazolyl N-substituted piperidine and imidazoline salts as potential agonists of M1 muscarinic receptors

(Chemical Equation Presented) Furanyl and oxazolyl N-substituted imidazoline salts were prepared by reacting furanyl and oxazolyl esters with ethylenediamine and trimethyl aluminum, followed by the addition of methyl iodide or hydrogen chloride. The piperidinium salts were prepared by treating furanyl and oxazolyl chlorides with piperidine base, followed by the addition of methyl iodide or hydrogen chloride.

Gonadotropin releasing hormone receptor antagonists

The present invention relates to Gonadotropin Releasing Hormone (“GnRH”) (also known as Leutinizing Hormone Releasing Hormone) receptor antagonists.