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4-Bromo-1-chloroisoquinoline

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Products Intro: Product Name:4-Bromo-1-chloroisoquinoline
CAS:66728-98-1
Purity:>=97% Package:0.1g;0.25g;1g;5g;10g;25g;100g
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Products Intro: Product Name:4-bromo-1-chloroisoquinoline
CAS:66728-98-1
Purity:98%(Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:4-Bromo-1-chloroisoquinoline
CAS:66728-98-1
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Products Intro: Product Name:4-Bromo-1-chloroisoquinoline
CAS:66728-98-1
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-01073
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Products Intro: Product Name:4-Bromo-1-chloroisoquinoline
CAS:66728-98-1
Purity:0.98 Package:1g;5g;25g;100;500g

4-Bromo-1-chloroisoquinoline manufacturers

4-Bromo-1-chloroisoquinoline Basic information
Product Name:4-Bromo-1-chloroisoquinoline
Synonyms:4-BROMO-1-CHLOROISOQUINOLINE;1-Chloro-4-bromoisoquinoline;4-Bromo-1-chloro-2-azanaphthalene;Isoquinoline, 4-bromo-1-chloro-;4-BROMO-1-CHLOROISOQUINOLINE 66728-98-1
CAS:66728-98-1
MF:C9H5BrClN
MW:242.5
EINECS:676-392-8
Product Categories:CHIRAL CHEMICALS
Mol File:66728-98-1.mol
4-Bromo-1-chloroisoquinoline Structure
4-Bromo-1-chloroisoquinoline Chemical Properties
Melting point 97 °C (decomp)
Boiling point 328.8±22.0 °C(Predicted)
density 1.673±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka-0.02±0.31(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C9H5BrClN/c10-8-5-12-9(11)7-4-2-1-3-6(7)8/h1-5H
InChIKeyHRWILRGBDZGABZ-UHFFFAOYSA-N
SMILESC1(Cl)C2=C(C=CC=C2)C(Br)=CN=1
CAS DataBase Reference66728-98-1(CAS DataBase Reference)
Safety Information
HS Code 2933499090
MSDS Information
4-Bromo-1-chloroisoquinoline Usage And Synthesis
Uses4-Bromo-1-chloroisoquinoline is an isoquinoline derivative whose molecular structure contains substituents chlorine and bromine atoms at positions 1 and 4. The product can be used in metal-catalysed cross-coupling reactions and in the preparation of pharmaceuticals.
Synthesis
4-BROMO-1(2H)-ISOQUINOLONE

3951-95-9

4-Bromo-1-chloroisoquinoline

66728-98-1

The general procedure for the synthesis of 4-bromo-1-chloroisoquinolines from 4-bromo-1(2H)-isoquinolinones was as follows: 4-bromoisoquinolin-1-ol (1.4 g, 5.80 mmol) was mixed with phosphorus trichloride (POCl3, 8.9 g, 58.09 mmol, 10 equiv.) and heated to reflux under stirring conditions. The progress of the reaction was monitored by liquid chromatography-mass spectrometry (LCMS) and it was confirmed that the reaction was completed after 4 hours. The reaction mixture was cooled to room temperature and the reaction was quenched with ice water (100 mL) followed by extraction with ethyl acetate (EtOAc, 3 x 25 mL). The organic phases were combined and washed sequentially with water (3 × 20 mL), saturated aqueous sodium bicarbonate (30 mL) and brine (20 mL). The organic layer was dried with anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent to afford 4-bromo-1-chloroisoquinoline as a white solid 1.3 g in 87% yield.

References[1] Bioorganic and Medicinal Chemistry Letters, 2017, vol. 27, # 2, p. 217 - 222
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