120427-95-4

  • Product Name:4-(2'-Bromoethyl)-3-Chloro-1,3-Dihydro-2-Indolinone
  • Molecular Formula:C10H9BrClNO
  • Purity:99%
  • Molecular Weight:274.545
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Product Details;

CasNo: 120427-95-4

Molecular Formula: C10H9BrClNO

Factory Export Top Purity 4-(2'-Bromoethyl)-3-Chloro-1,3-Dihydro-2-Indolinone 120427-95-4 In Stock

  • Molecular Formula:C10H9BrClNO
  • Molecular Weight:274.545
  • Vapor Pressure:0mmHg at 25°C 
  • Refractive Index:1.633 
  • Boiling Point:374.736 °C at 760 mmHg 
  • PKA:12.08±0.40(Predicted) 
  • Flash Point:180.434 °C 
  • PSA:29.10000 
  • Density:1.647 g/cm3 
  • LogP:2.99400 

4-(2'-BROMOETHYL)-3-CHLORO-1,3-DIHYDRO-2H-INDOLE-2-ONE(Cas 120427-95-4) Usage

InChI:InChI=1/C10H9BrClNO/c11-5-4-6-2-1-3-7-8(6)9(12)10(14)13-7/h1-3,9H,4-5H2,(H,13,14)

120427-95-4 Relevant articles

Preparation method of 4-(2-bromoethyl)-1, 3-dihydro-2H-indole-2-ketone

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Paragraph 0032; 0035; 0036; 0040; 0043-0044; 0048; 0051-0052, (2021/05/05)

The invention provides a preparation met...

PROCESS FOR PURIFICATION OF ROPINIROLE

-

Page/Page column 21-22, (2010/02/13)

The invention discloses an improved proc...

Development of large-scale syntheses of ropinirole in the pursuit of a manufacturing process

Hayler, John D.,Howie, Simon L. B.,Giles, Robert G.,Negus, Alan,Oxley, Paul W.,Walsgrove, Timothy C.,Whiter

, p. 3 - 9 (2013/09/08)

Two plant syntheses of ropinirole {4-[2-...

Some synthetic approaches to ropinirole (SK and F 101468-A): A potent dopamine receptor agonist

Hayler,Howie,Giles,Negus,Oxley,Walsgrove,Walsh,Dagger,Fortunak,Mastrocola

, p. 875 - 882 (2007/10/02)

Three new routes to ropinirole (SK and F...

120427-95-4 Process route

2-(2-bromoethyl)benzaldehyde
22901-09-3

2-(2-bromoethyl)benzaldehyde

4-(2-bromoethyl)-3-chloro-1,3-dihydro-2H-indolin-2-one
120427-95-4

4-(2-bromoethyl)-3-chloro-1,3-dihydro-2H-indolin-2-one

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: 80 percent / MeONa / methanol / 1 h / 0 °C
2: 53 percent / AcCl, FeCl3 / CH2Cl2 / 3 h / 0 - 5 °C
With sodium methylate; iron(III) chloride; acetyl chloride; In methanol; dichloromethane;
 
2-(2-bromoethyl)-β-nitrostyrene
120427-94-3

2-(2-bromoethyl)-β-nitrostyrene

4-(2-bromoethyl)-3-chloro-1,3-dihydro-2H-indolin-2-one
120427-95-4

4-(2-bromoethyl)-3-chloro-1,3-dihydro-2H-indolin-2-one

Conditions
Conditions Yield
With iron(III) chloride; acetyl chloride; In dichloromethane; at 0 - 5 ℃; for 3h;
83.9%

120427-95-4 Upstream products

  • 120427-94-3
    120427-94-3

    2-(2-bromoethyl)-β-nitrostyrene

  • 22901-09-3
    22901-09-3

    2-(2-bromoethyl)benzaldehyde

  • 75-36-5
    75-36-5

    acetyl chloride

  • 493-05-0
    493-05-0

    isochromane

120427-95-4 Downstream products

  • 120427-96-5
    120427-96-5

    4-(2'-bromoethyl)-1,3-dihydro-2H-indol-2-one

  • 91374-21-9
    91374-21-9

    Ropinirole

  • 120427-93-2
    120427-93-2

    4-ethylenyl-1,3-dihydro-2H-indol-2-one

  • 139122-19-3
    139122-19-3

    4-(2'-hydroxyethyl)-1,3-dihydro-2H-indol-2-one

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