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3279-90-1

6-bromo-3,4-dihydroquinolin-2(1H)-one

CAS: 3279-90-1

Molecular Formula: C9H8BrNO

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3279-90-1 - Names and Identifiers

Name 6-bromo-3,4-dihydroquinolin-2(1H)-one
Synonyms 3279-90-1
6-Bromocarbostiryl
6-BroMo-3,4-dihydrocarbostyril
6-BROMO-3,4-DIHYDROQUINOLIN-2(1H)-ONE
6-bromo-3,4-dihydroquinolin-2(1H)-one
6-Bromo-3,4-dihydroquinolin-2(1H)-one
6-BROMO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE
6-BROMO-3,4-DIHYDRO-2(1H)-QUINOLINONE
6-BroMo-3,4-dihydro-(1H)-2-quinolinone
2(1H)-Quinolinone, 6-bromo-3,4-dihydro-
6-BROMO-1,2,3,4-TETRAHYDRO-2-QUINOLINONE
6-Bromo-2-oxo-1,2,3,4-tetrahydroquinoline
CAS 3279-90-1
InChI InChI=1/C9H8BrNO/c10-7-2-3-8-6(5-7)1-4-9(12)11-8/h2-3,5H,1,4H2,(H,11,12)

3279-90-1 - Physico-chemical Properties

Molecular FormulaC9H8BrNO
Molar Mass226.07
Density1.559±0.06 g/cm3(Predicted)
Melting Point170-172℃
Boling Point376.3±42.0 °C(Predicted)
Flash Point181.352°C
Vapor Presure0mmHg at 25°C
AppearancePowder
ColorBrown
pKa13.92±0.20(Predicted)
Storage ConditionKeep in dark place,Sealed in dry,Room Temperature
SensitiveLight Sensitive
Refractive Index1.6

3279-90-1 - Risk and Safety

Hazard SymbolsXn - Harmful
Harmful
Risk CodesR36/37/38 - Irritating to eyes, respiratory system and skin.
R52 - Harmful to aquatic organisms
R22 - Harmful if swallowed
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.

3279-90-1 - Reference Information

application 6-bromo -1,2,3, 4-tetrahydro-2-quinolinone can be used as an intermediate in organic synthesis and a pharmaceutical intermediate, mainly used in laboratory research and development and chemical production.
preparation 3, 4-dihydroquinoline -2(1H)-one (2.73g,18.55mmol) was dissolved in N,N-dimethylacetamide (30mL), and N-bromosuccinimide (3.30g) was slowly added in an ice water bath, 18.55mmol) of N,N-dimethylacetamide (10mL) solution. The reaction solution continued to be stirred in an ice water bath for 6 hours and then heated to room temperature for 12 hours. After the reaction, water (50mL) was added to the reaction mixture and extracted with ethyl acetate (50mL × 3). The organic phases were combined, dried with anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (petroleum ether/ethyl acetate (v/v)= 3/1) to obtain a white solid (3.86g,92.1%).
Last Update:2024-04-09 21:54:55
3279-90-1
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