ChemicalBook > CAS DataBase List > 8-CHLOROQUINAZOLIN-4(1H)-ONE

8-CHLOROQUINAZOLIN-4(1H)-ONE

Product Name
8-CHLOROQUINAZOLIN-4(1H)-ONE
CAS No.
101494-95-5
Chemical Name
8-CHLOROQUINAZOLIN-4(1H)-ONE
Synonyms
8-chloroquinazolin-4-ol;8-chloroquinazolin-4(3H)-one;8-CHLOROQUINAZOLIN-4(1H)-ONE;8-Chloro-3H-quinazolin-4-one;4(3H)-Quinazolinone, 8-chloro-;8-chloro-3,4-dihydroquinazolin-4-one;8-CHLOROQUINAZOLIN-4(1H)-ONE, 10 mM in DMSO;8 CHLOROQUINAZOLIN 4(1H) ONE,8CHLOROQUINAZOLIN4(1H)ONE
CBNumber
CB62454854
Molecular Formula
C8H5ClN2O
Formula Weight
180.59
MOL File
101494-95-5.mol
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8-CHLOROQUINAZOLIN-4(1H)-ONE Property

Melting point:
302℃
Boiling point:
327.4±44.0 °C(Predicted)
Density 
1.50±0.1 g/cm3 (20 ºC 760 Torr)
storage temp. 
Sealed in dry,Room Temperature
form 
solid
pka
0.05±0.20(Predicted)
color 
Off-white
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Safety

HS Code 
2933998090
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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

H335May cause respiratory 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
C382033
Product name
8-Chloroquinazolin-4(3H)-one
Packaging
500mg
Price
$110
Updated
2021/12/16
TRC
Product number
C382033
Product name
8-Chloroquinazolin-4(3H)-one
Packaging
50mg
Price
$45
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC142506
Product name
8-Chloroquinazolin-4-ol
Packaging
1g
Price
$78
Updated
2021/12/16
Apolloscientific
Product number
OR946042
Product name
8-Chloroquinazolin-4(3H)-one
Purity
95%
Packaging
1g
Price
$185
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC142506
Product name
8-Chloroquinazolin-4-ol
Packaging
2g
Price
$135
Updated
2021/12/16
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8-CHLOROQUINAZOLIN-4(1H)-ONE Chemical Properties,Usage,Production

Uses

8-Chloroquinazolin-4-ol (Compd 18) is a PARP-1 enzyme inhibitor, with an IC50 of 5.65 μM[1].

Synthesis

6388-47-2

77287-34-4

101494-95-5

General procedure: 2-amino-3-chlorobenzoic acid (1 eq.) and an excess of formamide (6 eq.) were added to a three-necked flask. The reaction mixture was heated at 140 °C for 4-6 h. The progress of the reaction was monitored by thin layer chromatography (TLC). After completion of the reaction, ice water was added to the mixture. The precipitated solid was filtered, washed with water and subsequently dissolved in ethyl acetate, dried over anhydrous magnesium sulfate and concentrated to give pure 8-chloroquinazolin-4-ol. If the product did not precipitate, the reaction mixture was extracted with ethyl acetate, dried over anhydrous magnesium sulfate and concentrated to give quinazolin-4(3H)-one derivatives 1-9,11-15,17-21 and 23. Generic method for the preparation of amino derivatives 10,16 and 22: Substituted nitroquinazolin-4(3H)-one derivatives (0.3 g, 1.56 mmol), 6 mL of ethyl acetate and stannous chloride dihydrate (2.12 g, 9.42 mmol) were added to a reaction flask and the mixture was refluxed for 8 hours. After cooling to room temperature, the reaction was quenched with saturated sodium bicarbonate solution and subsequently extracted with ethyl acetate (3 x 50 mL). The organic layers were combined, dried over anhydrous magnesium sulfate and concentrated to afford the target amino-substituted quinazolin-4(3H)-one derivatives 10,16 and 22. The substituted o-aminobenzoic acid (1 g) was dissolved in excess acetic anhydride (10 mL) and stirred at room temperature for 4-7 h. The reaction progress was monitored by TLC. After removal of the solvent under vacuum, the residue was stirred with aqueous ammonia solution for 7 hours. After completion of the reaction, it was extracted with ethyl acetate (3 x 10 mL), the organic phases were combined, dried and concentrated with anhydrous magnesium sulfate to give compounds 26-30,31a and 32. The reduction of 2-methyl-8-nitroquinazolin-4(3H)-one intermediate (31a) to compound 31 was carried out in the same manner as described above for the synthesis of compounds 10,16 and 22.

References

[1] Shridhar S Kulkarni, et al. Synthesis and SAR optimization of quinazolin-4(3H)-ones as poly(ADP-ribose)polymerase-1 inhibitors. Eur J Med Chem. 2012 Apr:50:264-73. DOI:10.1016/j.ejmech.2012.02.001

8-CHLOROQUINAZOLIN-4(1H)-ONE Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from 8-CHLOROQUINAZOLIN-4(1H)-ONE manufacturers

Career Henan Chemical Co
Product
8-CHLOROQUINAZOLIN-4(1H)-ONE 101494-95-5
Price
US $1.00/KG
Min. Order
1KG
Purity
95%
Supply Ability
200KG
Release date
2018-08-19

101494-95-5, 8-CHLOROQUINAZOLIN-4(1H)-ONERelated Search:


  • 8-CHLOROQUINAZOLIN-4(1H)-ONE
  • 8-chloroquinazolin-4(3H)-one
  • 8-chloroquinazolin-4-ol
  • 8-chloro-3,4-dihydroquinazolin-4-one
  • 4(3H)-Quinazolinone, 8-chloro-
  • 8-Chloro-3H-quinazolin-4-one
  • 8 CHLOROQUINAZOLIN 4(1H) ONE,8CHLOROQUINAZOLIN4(1H)ONE
  • 8-CHLOROQUINAZOLIN-4(1H)-ONE, 10 mM in DMSO
  • 101494-95-5