14527-42-5

Basic information

• Product Name: Ethyl thiazole-2-carboxylate
• Synonyms: Ethyl thiazole-2-carboxylate;2-Thiazolecarboxylic acid, ethyl ester;2-(Ethoxycarbonyl)thiazole
• CAS NO: 14527-42-5
• Molecular Formula: C₆H₇NO₂S
• Molecular Weight: 157.19
• Mol File: 14527-42-5.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 226.525 °C at 760 mmHg
• Flash Point: 90.8 °C
• Appearance: /
• Density: 1.242 g/cm³
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Ethyl thiazole-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl thiazole-2-carboxylate(14527-42-5)
• EPA Substance Registry System: Ethyl thiazole-2-carboxylate(14527-42-5)

Safety Data

• Hazardous Substances Data: 14527-42-5(Hazardous Substances Data)

Usage

General Description

Ethyl thiazole-2-carboxylate is a chemical compound with the molecular formula C7H7NO2S. It is a colorless to pale yellow liquid with a pungent odor. Ethyl thiazole-2-carboxylate is commonly used as a flavoring agent and fragrance ingredient in the food, beverage, and cosmetic industries. It is also used in the production of pharmaceuticals and agricultural chemicals. Ethyl thiazole-2-carboxylate is known for its nutty, roasted, and meaty odor, and it is often used to impart these characteristics to products such as meat, baked goods, and savory snacks. Overall, this chemical plays a significant role in the creation of a wide variety of consumer products.

Upstream product

• 79265-30-8 2-(trimethylsilyl)thiazole 
• 541-41-3 chloroformic acid ethyl ester 
• 107-20-0 2-chloroethanal 
• 16982-21-1 ethyl 2-amino-2-thioxoacetate 
• 108-24-7 acetic anhydride 

Downstream Products

• 53101-04-5 ethyl 4-(4-nitrophenyl)-1,3-thiazole-2-carboxylate 
• 1006044-74-1 N-(1-methyl-1-phenylethyl)thiazole-2-carboxamide 
• 630422-15-0 N,N-diethyl-4-methoxy-2-(2-oxo-2-thiazol-2-yl-ethyl)-benzamide 
• 14542-12-2 (1,3-thiazol-2-yl)methanol 
• 16733-90-7 1,3-thiazole-2-carbohydrazide 
• 14190-59-1 1,3-thiazole-2-carboxylic acid 
• 16733-85-0 thiazole-2-carboxamide 
• 24295-03-2 2-Acetylthiazole 

Relevant articles and documents

REACTIONS OF 2-TRIMETHYLSILYLYHIAZOLE WITH ACYL CHLORIDES AND ALDEHYDES SYNTHESIS OF NEW THIAZOL-2-YL DERIVATES

2-Trimethylsilylthiazole (1) undergoes ipso-substitution of the silyl group with various acyl chlorides and ethyl chloroformate affording 2-acylthiazoles (2)-(5) but adds by the carbon-silicon bond to the carbonyl group of aldehydes yielding thiazol-2-yl-trimethylsiloxy-methane derivates (7).

PYRAZOLO[4,3-D]THIAZOLE DERIVATIVES, AND PREPARATION AND THERAPEUTIC APPLICATION THEREOF

The disclosure relates to a compound of formula (I): in which: R1, R2, R3 and R4 are as described in the specification, to compositions containing them and to their therapeutic use, especially as anticancer agen

1-(Aromatic- or heteroaromatic-substituted)-3-(heteroaromatic substituted)-1,3-propanediones and uses thereof

Certain 1-(aromatic- or heteroaromatic-substituted-3-(heteroaromatic substituted)-1,3-propanediones are described as inhibitors of HIV integrase and inhibitors of HIV replication. These compounds are useful in the prevention or treatment of infection by HIV and the treatment of AIDS, either as compounds, pharmaceutically acceptable salts, pharmaceutical composition ingredients, whether or not in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of treating AIDS and methods of preventing or treating infection by HIV are also described.