ChemicalBook > CAS DataBase List > 4-CHLORO-6-HYDROXYQUINAZOLINE

4-CHLORO-6-HYDROXYQUINAZOLINE

Product Name
4-CHLORO-6-HYDROXYQUINAZOLINE
CAS No.
848438-50-6
Chemical Name
4-CHLORO-6-HYDROXYQUINAZOLINE
Synonyms
183836;4-CHLOROQUINAZOLIN-6-OL;6-Quinazolinol, 4-chloro-;4-CHLORO-6-HYDROXYQUINAZOLINE
CBNumber
CB1378384
Molecular Formula
C8H5ClN2O
Formula Weight
180.59
MOL File
848438-50-6.mol
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4-CHLORO-6-HYDROXYQUINAZOLINE Property

storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
Off-white to light yellow Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
C895668
Product name
4-Chloroquinazolin-6-ol
Packaging
50mg
Price
$220
Updated
2021/12/16
AK Scientific
Product number
2702AL
Product name
4-Chloroquinazolin-6-ol
Packaging
1g
Price
$990
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0104895
Product name
4-CHLOROQUINAZOLIN-6-OL
Purity
95.00%
Packaging
5MG
Price
$497.48
Updated
2021/12/16
Chemenu
Product number
CM217289
Product name
4-Chloroquinazolin-6-ol
Purity
95%
Packaging
1g
Price
$655
Updated
2021/12/16
Crysdot
Product number
CD11046996
Product name
4-Chloroquinazolin-6-ol
Purity
95+%
Packaging
1g
Price
$691
Updated
2021/12/16
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4-CHLORO-6-HYDROXYQUINAZOLINE Chemical Properties,Usage,Production

Synthesis

179246-11-8

848438-50-6

Step E: Preparation of 4-chloroquinazolin-6-ol: 4-chloroquinazolin-6-yl acetate (10.0 g, 44.9 mmol) was dissolved in a methanol solution of ammonia (200 mL, 7N), and the reaction was stirred for 1 hour at room temperature. Upon completion of the reaction, the reaction mixture was concentrated under reduced pressure to about 3 mL, and the residue was ground with ether to precipitate a tan solid which was collected by filtration and dried to give 4-chloroquinazolin-6-ol (6.50 g, 80% yield).

References

[1] Patent: EP2090575, 2009, A1. Location in patent: Page/Page column 62
[2] Patent: WO2005/26151, 2005, A1. Location in patent: Page/Page column 113
[3] Patent: WO2011/130459, 2011, A1. Location in patent: Page/Page column 60
[4] European Journal of Medicinal Chemistry, 2018, vol. 147, p. 130 - 149

4-CHLORO-6-HYDROXYQUINAZOLINE Preparation Products And Raw materials

Raw materials

Preparation Products

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4-CHLORO-6-HYDROXYQUINAZOLINE Suppliers

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