3-(3-lodopropyl)-7,8-dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one

  • CAS：148870-57-9
  • purity：99%
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Details

Factory Sells Best Quality 3-(3-lodopropyl)-7,8-dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one 148870-57-9 with stock

  • Molecular Formula: C15H18INO3
  • Molecular Weight: 387.217
  • Vapor Pressure: 2.64E-10mmHg at 25°C 
  • Refractive Index: 1.592 
  • Boiling Point: 504.51 °C at 760 mmHg 
  • PKA: -1.23±0.20(Predicted) 
  • Flash Point: 258.919 °C 
  • PSA： 38.77000 
  • Density: 1.514 g/cm3 
  • LogP: 2.82220 

7,8-Dimethoxy-3-(3-iodopropyl)-1,3-dihydro-2H-3-benzazepin-2-one(Cas 148870-57-9) Usage

General Description

7,8-Dimethoxy-3-(3-iodopropyl)-1,3-dihydro-2H-3-benzazepin-2-one is a chemical compound that consists of a benzazepine ring structure with two methoxy and one iodopropyl group attached to it. It belongs to the class of organic compounds known as flavonoids. 7,8-Dimethoxy-3-(3-iodopropyl)-1,3-dihydro-2H-3-benzazepin-2-one is not naturally occurring but has potential applications in medicinal chemistry and drug development due to its unique structure and properties. It may also have potential uses in research and experimental studies related to neurotransmitters and neuropharmacology. Further studies and research are needed to explore the full spectrum of its potential uses and applications.

InChI:InChI=1/C15H18INO3/c1-19-13-8-11-4-7-17(6-3-5-16)15(18)10-12(11)9-14(13)20-2/h4,7-9H,3,5-6,10H2,1-2H3

148870-57-9 Relevant articles

AN IMPROVED PROCESS FOR THE SYNTHESIS OF IVABRADINE AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS

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Page/Page column 19, (2019/11/12)

: Disclosed herein is an improved proces...

PROCESS FOR MAKING IVABRADINE

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Page/Page column 15; 16, (2014/08/07)

The invention relates to an improved pro...

PROCESS FOR PREPARATION OF IVABRADINE

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Paragraph 0121, (2014/07/21)

A process for the preparation of ivabrad...

IVABRADINE HYDROCHLORIDE AND THE PROCESSES FOR PREPARATION THEREOF

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Page/Page column 13, (2014/02/16)

The present disclosure relates to a proc...

148870-57-9 Process route

3-(3-chloropropyl)-1,3-dihydro-7,8-dimethoxy-2H-3-benzazepine-2-one
85175-59-3

3-(3-chloropropyl)-1,3-dihydro-7,8-dimethoxy-2H-3-benzazepine-2-one

7,8-dimethoxy-3-[3-iodopropane]-1,3-dihydro-2H-3-benzazepin-2-one
148870-57-9

7,8-dimethoxy-3-[3-iodopropane]-1,3-dihydro-2H-3-benzazepin-2-one

Conditions
Conditions Yield
99%
3-(3-chloropropyl)-1,3-dihydro-7,8-dimethoxy-2H-3-benzazepine-2-one
85175-59-3

3-(3-chloropropyl)-1,3-dihydro-7,8-dimethoxy-2H-3-benzazepine-2-one

7,8-dimethoxy-3-[3-iodopropane]-1,3-dihydro-2H-3-benzazepin-2-one
148870-57-9

7,8-dimethoxy-3-[3-iodopropane]-1,3-dihydro-2H-3-benzazepin-2-one

Conditions
Conditions Yield
With sodium iodide; at 117 - 118 ℃; Inert atmosphere;
92%
With sodium iodide; In butanone; for 8h; Reflux;
86%
With sodium iodide; In acetone; for 24h; Solvent; Time; Concentration; Reflux;
85%
With sodium iodide; In acetone; for 12h; Heating;
With sodium iodide; In acetone; at 25 - 65 ℃; for 30h; Reflux;
With sodium iodide; In acetone; at 55 - 58 ℃; for 20h;

148870-57-9 Upstream products

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    7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one

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    2-(3,4-dimethoxyphenyl)acetamide

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148870-57-9 Downstream products

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    1086026-31-4

    3-{3-[{[(7S)-3,4-dimethoxybicyclo[4.2.0]octa-1,3,5-trien-7-yl]methyl}-(methyl)amino]propyl}-7,8-dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one

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    ivabradine

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