4-chloro-2-(4-chloro-1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,2-dihydro-3H-indol-3-one

  • Name: 4-chloro-2-(4-chloro-1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,2-dihydro-3H-indol-3-one
  • CAS: 6275-44-1
  • Purity: 99%
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4-chloro-2-(4-chloro-1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,2-dihydro-3H-indol-3-one 6275-44-1 with purity >99% Low price in stock

  • Molecular Formula: C16H8 Cl2 N2 O2
  • Molecular Weight: 331.158
  • Vapor Pressure: 9.37E-09mmHg at 25°C 
  • Boiling Point: 463.1°C at 760 mmHg 
  • Flash Point: 233.9°C 
  • PSA： 58.20000 
  • Density: 1.584g/cm3 
  • LogP: 4.39760 

4-chloro-2-(4-chloro-1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,2-dihydro-3H-indol-3-one(Cas 6275-44-1) Usage

General Description

4-chloro-2-(4-chloro-1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,2-dihydro-3H-indol-3-one is a complex chemical compound with a molecular formula C16H10Cl2N2O2. It is a yellowish solid with a molecular weight of 333.17 g/mol. 4-chloro-2-(4-chloro-1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,2-dihydro-3H-indol-3-one is a derivative of indole and contains two chlorine atoms. It is used in research and development in the pharmaceutical industry, and its potential applications include being used as a fluorescent labeling reagent for biological imaging and as a building block for the synthesis of various organic compounds. Its unique structure and properties make it a valuable chemical for scientific investigation and product development.

InChI:InChI=1/C16H8Cl2N2O2/c17-7-3-1-5-9-11(7)15(21)13(19-9)14-16(22)12-8(18)4-2-6-10(12)20-14/h1-6,19-20H

6275-44-1 Relevant articles

High-Performance Ambipolar Polymers Based on Electron-Withdrawing Group Substituted Bay-Annulated Indigo

Yang, Jie,Jiang, Yaqian,Tu, Zeyi,Zhao, Zhiyuan,Chen, Jinyang,Yi, Zhengran,Li, Yifan,Wang, Shuai,Yi, Yuanping,Guo, Yunlong,Liu, Yunqi

, (2019/01/05)

For donor–acceptor conjugated polymers, ...

Exploring the biocatalytic scope of a bacterial flavin-containing monooxygenase

Rioz-Martinez, Ana,Kopacz, Malgorzata,De Gonzalo, Gonzalo,Torres Pazmino, Daniel E.,Gotor, Vicente,Fraaije, Marco W.

experimental part, p. 1337 - 1341 (2011/04/23)

A bacterial flavin-containing monooxygen...

Styrene monooxygenase from Pseudomonas sp. LQ26 catalyzes the asymmetric epoxidation of both conjugated and unconjugated alkenes

Lin, Hui,Qiao, Jing,Liu, Yan,Wu, Zhong-Liu

experimental part, p. 236 - 241 (2011/02/22)

A novel styrene monooxygenase (SMO) was ...

6275-44-1 Process route

2-chloro-6-nitrobenzaldehyde
6361-22-4

2-chloro-6-nitrobenzaldehyde

acetone
67-64-1

acetone

4,4'-diCl-indigo
6275-44-1

4,4'-diCl-indigo

Conditions
Conditions Yield
With sodium hydroxide;
With sodium hydroxide; 4,4'-dichloro-indigo;
With sodium hydroxide;
With sodium hydroxide; In water;
4-chloro-1H-indole
25235-85-2

4-chloro-1H-indole

4,4'-diCl-indigo
6275-44-1

4,4'-diCl-indigo

Conditions
Conditions Yield
With sodium phosphite; NADPH; sodium chloride; at 25 ℃; for 18h; pH=8.5; aq. buffer; Enzymatic reaction;

6275-44-1 Upstream products

  • 6361-22-4
    6361-22-4

    2-chloro-6-nitrobenzaldehyde

  • 67-64-1
    67-64-1

    acetone

  • 25235-85-2
    25235-85-2

    4-chloro-1H-indole

  • 114382-39-7
    114382-39-7

    acetic acid-(4-chloro-indol-3-yl ester)

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