6-Bromo-3,4-dihydro-1H-quinolin-2-one

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Company Name: Jinan SanZhi Pharmaceutical Technology Co., Ltd.  Gold
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6-Bromo-3,4-dihydro-1H-quinolin-2-one manufacturers

6-Bromo-3,4-dihydro-1H-quinolin-2-one Basic information
Product Name:6-Bromo-3,4-dihydro-1H-quinolin-2-one
Synonyms:6-Bromocarbostiryl;6-BroMo-3,4-dihydrocarbostyril;6-BROMO-3,4-DIHYDRO-2(1H)-QUINOLINONE;6-Bromo-3,4-dihydro-2(1H)-quinolinone 98%;2(1H)-Quinolinone, 6-bromo-3,4-dihydro-;Carbostyril, 6-bromo-3,4-dihydro-;6-broMo-1,2,3,4-tetrahydroquinolin-2-one;6-BroM-3,4-dihydro-carbostyril
CAS:3279-90-1
MF:C9H8BrNO
MW:226.07
EINECS:
Product Categories:
Mol File:3279-90-1.mol
6-Bromo-3,4-dihydro-1H-quinolin-2-one Structure
6-Bromo-3,4-dihydro-1H-quinolin-2-one Chemical Properties
Melting point 170-172℃
Boiling point 376.3±42.0 °C(Predicted)
density 1.559±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka13.92±0.20(Predicted)
form Powder
color Brown
Sensitive Light Sensitive
InChIInChI=1S/C9H8BrNO/c10-7-2-3-8-6(5-7)1-4-9(12)11-8/h2-3,5H,1,4H2,(H,11,12)
InChIKeyMQWZSSIUHXNNTM-UHFFFAOYSA-N
SMILESN1C2=C(C=C(Br)C=C2)CCC1=O
CAS DataBase Reference3279-90-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 36/37/38-52-22
Safety Statements 26-36/37/39
HS Code 2933499090
MSDS Information
6-Bromo-3,4-dihydro-1H-quinolin-2-one Usage And Synthesis
Synthesis3,4-Dihydroquinolin-2(1H)-one (2.73 g, 18.55 mmol) was dissolved in N,N-dimethylacetamide (30 mL) and N,N-dimethylacetamide (10 mL) solution of N-bromosuccinimide (3.30 g, 18.55 mmol) was added slowly and dropwise in an ice water bath. The reaction solution continued to react in an ice water bath with stirring for 6 hours and then warmed up to room temperature for 12 hours. At the end of the reaction, water (50 mL) was added to the reaction mixture and extracted with ethyl acetate (50 mL x 3). The organic phases were combined, dried with anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (petroleum ether/ethyl acetate (v/v) = 3/1) to afford the title compound as a white solid (3.86 g, 92.1%).
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