607-69-2

Basic information

• Product Name: 2-CHLORO-4-HYDROXYQUINAZOLINE
• Synonyms: 2-CHLORO-4-HYDROXYQUINAZOLINE;2-chloroquinazolin-4-ol;4(3H)-Quinazolinone, 2-chloro-;2-Chloro-4(1H)-quinazolinone;2-Chloroquinazolin-4-one;2-Chloroquinazolin-4(3H)
• CAS NO: 607-69-2
• Molecular Formula: C₈H₅ClN₂O
• Molecular Weight: 180.59
• Mol File: 607-69-2.mol
• Article Data: 2

Chemical Properties

• Melting Point: 218-220℃
• Boiling Point: 325.9 °C at 760 mmHg
• Flash Point: 150.9 °C
• Appearance: /
• Density: 1.50
• Vapor Pressure: 0.000223mmHg at 25°C
• Refractive Index: 1.688
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: -2.12±0.20(Predicted)
• CAS DataBase Reference: 2-CHLORO-4-HYDROXYQUINAZOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLORO-4-HYDROXYQUINAZOLINE(607-69-2)
• EPA Substance Registry System: 2-CHLORO-4-HYDROXYQUINAZOLINE(607-69-2)

Safety Data

• Hazardous Substances Data: 607-69-2(Hazardous Substances Data)

Usage

General Description

2-CHLORO-4-HYDROXYQUINAZOLINE is a chemical compound that belongs to the quinazoline class of organic compounds. It is a chlorinated derivative of 4-hydroxyquinazoline and is commonly used in the pharmaceutical industry for the synthesis of various drugs and biologically active compounds. 2-CHLORO-4-HYDROXYQUINAZOLINE has been studied for its potential as an antitumor agent and has shown promising results in inhibiting the growth of cancer cells. Additionally, 2-CHLORO-4-HYDROXYQUINAZOLINE has also been investigated for its antimicrobial and antiviral properties, making it a versatile compound with potential applications in the development of new drugs and therapeutic agents.

InChI:InChI=1/C8H5ClN2O/c9-8-10-6-4-2-1-3-5(6)7(12)11-8/h1-4H,(H,10,11,12)

Upstream product

• 124-48-1 chlorodibromomethane 
• 28144-70-9 anthranilic acid amide 
• 120-94-5 1-Methylpyrrolidine 
• 86-96-4 1,2,3,4-tetrahydro-quinazoline-2,4-dione 

Downstream Products

• 60420-44-2 2-[(4-chlorophenyl)amino]quinazolin-4(3H)-one 
• 1913-19-5 2-((4-methoxyphenyl)amino)quinazolin-4(3H)-one 
• 4248-15-1 2-anilinoquinazolin-4(3H)-one 
• 857763-49-6 2-(4-chloro-phenylsulfanyl)-3H-quinazolin-4-one 
• 92872-11-2 2-(4-oxo-3,4-dihydro-quinazolin-2-ylamino)-benzoic acid methyl ester 
• 52727-44-3 2,3-dihydro-5H-oxazolo<2,3-b>quinazolin-5-one 
• 607-68-1 2,4-dichloroquinazoline 
• 1011-24-1 2-methoxy-3,4-dihydro-4-oxoquinazoline 
• 109791-95-9 2-[4-(3-Piperidin-1-ylmethyl-phenoxy)-butylamino]-3H-quinazolin-4-one 
• 105150-87-6 2-<3-<3-(1-piperidinylmethyl)phenoxy>propylamino>-4(3H)-quinazoline 
• 119023-23-3 2-(3-m-Tolyloxy-propylamino)-3H-quinazolin-4-one 
• 6499-59-8 2-((4-hydroxyphenyl)amino)quinazolin-4(3H)-one 
• 105150-86-5 2-[3-(3-Pyrrolidin-1-ylmethyl-phenoxy)-propylamino]-3H-quinazolin-4-one 
• 100448-60-0 2-((4-carboxyphenyl)amino)quinazolin-4(3H)-one 

Relevant articles and documents

NOVEL COMPOUND FOR ORGANIC ELECTROLUMINESCENT DEVICE AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME

Disclosed are a compound for an organic electroluminescent device, and an organic electroluminescent device comprising the same. Accordingly, provided is a compound for an organic electroluminescent device, which can be used as a host and a hole transport material having excellent electrical stability and hole transporting capability and improving light emitting efficiency of a phosphorescent material by having a high triplet energy. An organic electroluminescent device is also provided. The compound for an organic electroluminescent device is represented by structural formula 1.COPYRIGHT KIPO 2016