5198-87-8 - Names and Identifiers
5198-87-8 - Physico-chemical Properties
Molecular Formula | C4H2ClNO2S
|
Molar Mass | 163.58 |
Density | 1.693±0.06 g/cm3(Predicted) |
Melting Point | 220 °C |
Boling Point | 370.2±34.0 °C(Predicted) |
Flash Point | 177.696°C |
Vapor Presure | 0mmHg at 25°C |
Appearance | Crystalline Powder |
Color | White to yellow |
pKa | 3.15±0.10(Predicted) |
Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
Refractive Index | 1.634 |
5198-87-8 - Risk and Safety
Hazard Symbols | Xi - Irritant

|
WGK Germany | 3 |
Hazard Class | IRRITANT |
5198-87-8 - Introduction
2-Chloro-1,3-thiazole-4-carboxylic acid is an organic compound with the molecular formula C4H3ClN2O2S and a thiazole ring and carboxylic acid functional group in the structure. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: 2-Chloro-1,3-thiazole-4-carboxylic acid is white to light yellow crystal.
-Melting point: about 150-153 degrees Celsius.
-Solubility: 2-Chloro-1,3-thiazole-4-carboxylic acid has good solubility in common organic solvents, such as alcohols, ethers and esters, but has low solubility in water.
-chemical properties: 2-Chloro-1,3-thiazole-4-carboxylic acid can react with other compounds, such as reacting with amines to generate corresponding amides, nucleophilic addition reactions with nucleophiles, etc.
Use:
-Pharmaceutical intermediates: 2-Chloro-1,3-thiazole-4-carboxylic acid, as pharmaceutical intermediates, is widely used in the pharmaceutical field and can be used to synthesize some biologically active compounds.
-Pesticide intermediates: 2-Chloro-1,3-thiazole-4-carboxylic acid can also be used as pesticide intermediates for the synthesis of pesticide products.
-Other uses: In addition, 2-Chloro-1,3-thiazole-4-carboxylic acid can also be used as chemical reagents and catalysts.
Preparation Method:
The preparation method of 2-Chloro-1,3-thiazole-4-carboxylic acid is usually carried out by the following steps:
1. react 2-chloro -4-thiazolecarbonyl chloride (n) with alkali (such as sodium carbonate) or alkaline medium (such as sodium hydroxide) to generate 2-Chloro-1,3-thiazole-4-carboxylic acid sodium (n).
2.2-Chloro-1,3-thiazole-4-carboxylic acid sodium is reacted with dilute acid (such as dilute hydrochloric acid) to give 2-Chloro-1,3-thiazole-4-carboxylic acid.
Safety Information:
2-Chloro-1,3-thiazole-4-carboxylic acid belongs to organochlorine compounds, which have certain toxicity and should be paid attention to safe operation. The following safety measures shall be observed during use and storage:
-Avoid contact with skin and eyes, and wear appropriate protective equipment (such as gloves and goggles).
-Operate in a well-ventilated environment to avoid inhaling its vapor or dust.
-Store in a cool, dry, ventilated place, away from fire and oxidizing agents.
-Avoid reacting with strong oxidants to avoid unsafe situations.
When dealing with 2-Chloro-1,3-thiazole-4-carboxylic acid, it is best to follow relevant regulations and safety operation guidelines, and consult chemical experts when necessary.
Last Update:2024-04-09 21:32:42