8-BROMO-2H-ISOQUINOLIN-1-ONE

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Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:8-Bromoisoquinolin-1(2H)-one
CAS:475994-60-6
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-08698
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Products Intro: Product Name:8-BROMO-2H-ISOQUINOLIN-1-ONE
CAS:475994-60-6
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Company Name: Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
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Products Intro: Product Name:8-bromoisoquinolin-1-ol
CAS:475994-60-6
Purity:0.97 Package:1KG;25KG
Company Name: Win-Win chemical CO., Limited
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Products Intro: Product Name:8-Bromoisoquinolin-1(2H)-one
CAS:475994-60-6
Purity:95% Package:1kg,5kg,10kg
Company Name: Blocksynth Pharmaceutical Technology Co.,Ltd
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Products Intro: Product Name:8-BROMO-2H-ISOQUINOLIN-1-ONE
CAS:475994-60-6
Purity:98% Package:25KG;USD

8-BROMO-2H-ISOQUINOLIN-1-ONE manufacturers

8-BROMO-2H-ISOQUINOLIN-1-ONE Basic information
Product Name:8-BROMO-2H-ISOQUINOLIN-1-ONE
Synonyms:8-Bromoisoquinolin-1(2H)-one;8-BroMo-2H-isoquinoline-1-one;8-Bromo-1(2H)-isoquinolinone;8-BROMO-2H-ISOQUINOLIN-1-ONE;8-Bromoisoquinolin-1-ol;8-Bromo-1-hydroxyisoquinoline;8-Bromoisoquinolin-1(2H);8-bromo-1(2H)-isoquinolin-1-one
CAS:475994-60-6
MF:C9H6BrNO
MW:224.05
EINECS:
Product Categories:
Mol File:475994-60-6.mol
8-BROMO-2H-ISOQUINOLIN-1-ONE Structure
8-BROMO-2H-ISOQUINOLIN-1-ONE Chemical Properties
Boiling point 446.1±45.0 °C(Predicted)
density 1.620±0.06 g/cm3 (20 ºC 760 Torr)
storage temp. 2-8°C
pka11.81±0.20(Predicted)
form powder
color Yellow
InChIInChI=1S/C9H6BrNO/c10-7-3-1-2-6-4-5-11-9(12)8(6)7/h1-5H,(H,11,12)
InChIKeyNQMZAFRCYDJSEU-UHFFFAOYSA-N
SMILESC1(=O)C2=C(C=CC=C2Br)C=CN1
Safety Information
HS Code 2933499090
MSDS Information
8-BROMO-2H-ISOQUINOLIN-1-ONE Usage And Synthesis
Synthesis
8-Bromoisoquinoline 2-oxide

475994-58-2

8-BROMO-2H-ISOQUINOLIN-1-ONE

475994-60-6

The general procedure for the synthesis of 8-bromoisoquinolin-1(2H)-one from 8-bromoisoquinoline 2-oxide was as follows: 8-bromoisoquinoline 2-oxide (630 mg, 2.8 mmol) was suspended in N,N-dimethylformamide (DMF, 10 mL), and treated with trifluoroacetic anhydride (4 mL). The reaction mixture was stirred overnight at room temperature until the solution was clarified. Subsequently, the reaction solution was concentrated under reduced pressure to remove the solvent. The residue was neutralized with dilute aqueous sodium carbonate and extracted several times with a 5% methanol/dichloromethane mixture. The organic phases were combined, washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography, eluting with a gradient of 0-10% methanol in dichloromethane solution to give a white solid product (180 mg, 29% yield). Mass spectrometric analysis (positive ion electrospray mode) showed m/z 225 [M+H]+.

References[1] Patent: WO2004/2992, 2004, A1. Location in patent: Page 76; 77
[2] Tetrahedron, 2002, vol. 58, # 29, p. 5761 - 5766
[3] Patent: WO2017/100591, 2017, A1. Location in patent: Paragraph 00226
Tag:8-BROMO-2H-ISOQUINOLIN-1-ONE(475994-60-6) Related Product Information
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