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6-Chloro-4-hydroxyquinazoline(CAS#16064-14-5)

Chemical Property:

Molecular Formula C8H5ClN2O
Molar Mass 180.59
Density 1.4300 (rough estimate)
Melting Point 263-265 °C
Boling Point 128.9°C (rough estimate)
Flash Point 169.2°C
Vapor Presure 2.99E-05mmHg at 25°C
pKa 0.93±0.20(Predicted)
Storage Condition Sealed in dry,Room Temperature
Refractive Index 1.5430 (estimate)
MDL MFCD01686365

Product Detail

Product Tags

Hazard Symbols Xi - Irritant
Hazard Note Irritant

 

Introduction

Phenol, also known as chloroquinazoline phenol (Chloroxine), is an organic compound. The following is a description of its nature, use, preparation and safety information:

 

Nature:

-Appearance: White crystalline solid.

-Solubility: Its solubility in water is low, but it can be dissolved in organic solvents, such as ethanol and dichloromethane.

-Stability: The compound is relatively stable and not easy to decompose or degrade.

 

Use:

-Antibacterial agent: It has strong antibacterial properties and is widely used in personal care products, pharmaceutical preparations and disinfectants.

-Preservative: Due to its antibacterial properties, it is also often used as a preservative for products such as cosmetics and detergents.

-Non-ionic surfactant: It can be combined with other compounds to form a non-ionic surfactant, which is used in cleaners and detergents.

 

Method:

It can be obtained by reacting 3-chloro-1-hydroxyquinazoline with a phenolic compound. The specific preparation details require further laboratory research and process optimization.

 

Safety Information:

-It has low toxicity, but it still needs to be used carefully. In case of contact with skin and eyes, wash immediately. Avoid inhalation or ingestion.

-Store out of reach of children and pets.

-Dispose of waste in a suitable manner.

Application
6-Chloro-4-hydroxyquinazoline (CAS 16064-14-5) is a functionalized quinazolinone derivative bearing a chlorine atom at the 6-position. This heterocyclic building block is a key intermediate in medicinal chemistry and drug discovery, particularly for the synthesis of potent tyrosine kinase inhibitors (e.g., EGFR, HER2, and VEGFR inhibitors) for targeted cancer therapy. The 4-hydroxy/4-oxo tautomer provides hydrogen bond donor/acceptor sites, enhancing target binding affinity. The chlorine at C6 enables cross-coupling reactions (Suzuki-Miyaura, Buchwald-Hartwig, Sonogashira) for introducing diverse substituents, facilitating rapid structure-activity relationship studies. This scaffold is also utilized in developing antiviral, anti-inflammatory, and antimicrobial agents. High purity ensures reproducible results in high-throughput screening and scalable GMP manufacturing. Xinchem offers custom synthesis, custom chemical synthesis, and contract manufacturing of this API intermediate with flexible scaling from R&D to commercial tons. Contact us today for a competitive quote and reliable global supply.


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