ChemicalBook > CAS DataBase List > Quinazoline

Quinazoline

Product Name
Quinazoline
CAS No.
253-82-7
Chemical Name
Quinazoline
Synonyms
PHENMIAZINE;1,3-BENZODIAZINE;5,6-Benzopyrimidine;QUINAZOLINE;Quinazoline 99%;Benzopyrimidine;Quinazoline >Quinazoline ,98%;Benzo[d]pyrimidine;benzo[a]pyrimidine
CBNumber
CB8181293
Molecular Formula
C8H6N2
Formula Weight
130.15
MOL File
253-82-7.mol
More
Less

Quinazoline Property

Melting point:
46-48 °C (lit.)
Boiling point:
243 °C (lit.)
Density 
1.2002 (rough estimate)
refractive index 
1.6231 (estimate)
Flash point:
224 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
H2O: freely soluble
pka
3.43(at 20℃)
form 
Crystalline Powder, Crystals and/or Chunks
color 
Yellow to beige to brownish
Water Solubility 
H2O: freely soluble
organic solvents: soluble
Merck 
14,8053
BRN 
109370
CAS DataBase Reference
253-82-7(CAS DataBase Reference)
NIST Chemistry Reference
Quinazoline(253-82-7)
EPA Substance Registry System
Quinazoline (253-82-7)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
22-24/25-36-26-23
WGK Germany 
3
HS Code 
29339900
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
123323
Product name
Quinazoline
Purity
99%
Packaging
1g
Price
$75.7
Updated
2025/07/31
Sigma-Aldrich
Product number
123323
Product name
Quinazoline
Purity
99%
Packaging
5g
Price
$170.8
Updated
2025/07/31
TCI Chemical
Product number
Q0055
Product name
Quinazoline
Purity
>98.0%(GC)(T)
Packaging
1g
Price
$114
Updated
2025/07/31
TRC
Product number
Q670100
Product name
Quinazoline
Packaging
5g
Price
$120
Updated
2021/12/16
TRC
Product number
Q670100
Product name
Quinazoline
Packaging
25g
Price
$330
Updated
2021/12/16
More
Less

Quinazoline Chemical Properties,Usage,Production

Chemical Properties

Beige to brownish crystalline powder

Uses

Quinazoline was used to study the electrochemical behaviour of quinazoline using modern polarographic and voltammetric methods. It is the basic structural unit of pharmaceuticals and plays an important role in modern synthesis of antitumor drugs.

Definition

ChEBI: A mancude organic heterobicyclic parent that is naphthalene in which the carbon atoms at positions 1 and 3 have been replaced by nitrogen atoms.

General Description

Quinazolines has applications in medicinal chemistry due to their antibacterial, antifungal, anticonvulsant, anti-inflammatory and antitumor activities. It is the basic structural unit of pharmaceuticals and plays an important role in modern synthesis of antitumor drugs.

Biochem/physiol Actions

Genotoxicity of quinazoline was established by bacterial SOS Chromotest (Escherichia Coli).

Synthesis

5190-68-1

253-82-7

The general method for the synthesis of quinazoline from 4-chloroquinazoline was as follows: first, the halogenated heterocycle (0.66 mmol) was dissolved in anhydrous THF (13.2 mL) and degassed by drumming argon gas for several minutes. Subsequently, PdCl2 (dppf) (27.0 mg, 0.033 mmol, 5.0 mol%), TMEDA (0.130 g, 1.12 mmol, 1.7 equiv), and NaBH4 (42.4 mg, 1.12 mmol, 1.7 equiv) were added sequentially. The reaction mixture was stirred at room temperature for an appropriate time under argon protection, after which it was post-treated according to standard methods.

Purification Methods

Purify quinazoline by passage through an activated alumina column in *C6H6 or pet ether (b 40-60o). Distil it under reduced pressure, sublime it under vacuum and crystallise it from pet ether. The picrate has m 188-189o (from MeOH). [Armarego J Appl Chem 11 70 1961, Armarego Quinazolines, Fused Pyrimidines Part I Brown Ed, Wiley-Interscience 1967, Brown Quinazolines Supplement I Taylor Ed, Wiley-Interscience 1996, ISBN 0-471-14565-3; for covalent hydration see Albert & Armarego Adv Heterocycl Chem 4 1 1965, Beilstein 23 H 175, 23 II 177, 23 III/IV 1221.]

References

[1] Journal of Molecular Catalysis A: Chemical, 2014, vol. 393, p. 191 - 209

More
Less

Quinazoline Suppliers

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44801
Advantage
61
Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Fax
001-617-206-9595
Email
sales@chemreagents.com
Country
United States
ProdList
10186
Advantage
62
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42934
Advantage
64
Sichuan Kulinan Technology Co., Ltd
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11705
Advantage
57
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400 638 7771
Email
sales@heowns.com
Country
China
ProdList
14435
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9815
Advantage
79
More
Less

View Lastest Price from Quinazoline manufacturers

Career Henan Chemical Co
Product
Quinazoline 253-82-7
Price
US $98.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
100KG
Release date
2018-08-04

253-82-7, QuinazolineRelated Search:


  • 1,3-Diazanaphthalene
  • 4.5-Benzopyrimidine
  • Benzo(e)pyrimidine
  • 1,3-Benzodiazine, Benzopyrimidine
  • 5,6-Benzopyrimidine
  • Quinazoline ,98%
  • Benzo[d]pyrimidine
  • Benzopyrimidine
  • Quinazoline (6CI,8CI,9CI)
  • benzo[a]pyrimidine
  • Quinazoline 99%
  • PHENMIAZINE
  • QUINAZOLINE
  • 1,3-BENZODIAZINE
  • Quinazoline &gt
  • quinazoline - [Q22663]
  • 253-82-7
  • Heterocyclic Building Blocks
  • Building Blocks
  • Quinazolines
  • PYRIMIDINE