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3,4,5-Trichloroaniline

  • Product Name 3,4,5-Trichloroaniline
  • cas 634-91-3
  • purity 99%
Inquiry

Reputable factory supply 3,4,5-Trichloroaniline 634-91-3 in stock with high standard

  • Molecular Formula: C6H4Cl3N
  • Molecular Weight: 196.463
  • Appearance/Colour: beige crystalline powder 
  • Vapor Pressure: 0.000456mmHg at 25°C 
  • Melting Point: 97-99 ºC 
  • Refractive Index: 1.626 
  • Boiling Point: 314.8 ºC at 760 mmHg 
  • PKA: 1.85±0.10(Predicted) 
  • Flash Point: 144.2 ºC 
  • PSA: 26.02000 
  • Density: 1.54 g/cm3 
  • LogP: 3.81020 

3,4,5-Trichloroaniline(Cas 634-91-3) Usage

General Description

3,4,5-Trichloroaniline forms tri- and tetrachloroaniline-Pt(II) complexes having good antileukemic activity.

InChI:InChI=1/C6H4Cl3N/c7-4-1-3(10)2-5(8)6(4)9/h1-2H,10H2

634-91-3 Relevant articles

General and Chemoselective Copper Oxide Catalysts for Hydrogenation Reactions

Li, Wu,Cui, Xinjiang,Junge, Kathrin,Surkus, Annette-Enrica,Kreyenschulte, Carsten,Bartling, Stephan,Beller, Matthias

, p. 4302 - 4307 (2019/05/08)

Copper oxide catalysts have been prepare...

Nitrogen-Doped Graphene-Supported Iron Catalyst for Highly Chemoselective Hydrogenation of Nitroarenes

Wei, Zuojun,Hou, Yaxin,Zhu, Xinmiao,Guo, Liangyu,Liu, Yingxin,Zhang, Anyun

, p. 2009 - 2013 (2018/03/21)

A nitrogen-doped graphene-supported iron...

AMINATION AND HYDROXYLATION OF ARYLMETAL COMPOUNDS

-

Paragraph 0098; 0134; 0135; 0177, (2018/03/25)

In one aspect, the present disclosure pr...

Rapid heteroatom transfer to arylmetals utilizing multifunctional reagent scaffolds

Gao, Hongyin,Zhou, Zhe,Kwon, Doo-Hyun,Coombs, James,Jones, Steven,Behnke, Nicole Erin,Ess, Daniel H.,Kürti, László

, p. 681 - 688 (2017/06/30)

Arylmetals are highly valuable carbon nu...

634-91-3 Process route

3,4,5-trichloronitrobenzen
20098-48-0

3,4,5-trichloronitrobenzen

3,4,5-trichloroaniline
634-91-3

3,4,5-trichloroaniline

Conditions
Conditions Yield
With 2,3-dimethyl-2,3-butane diol; [MoO2Cl2(dmf)2]; In toluene; at 150 ℃; for 0.5h; chemoselective reaction; Microwave irradiation;
98%
With hydrogen; In toluene; at 140 ℃; for 48h; under 37503.8 Torr; chemoselective reaction;
80%
With thiophenol; In acetonitrile; for 2.5h; Ambient temperature; Irradiation;
14%
With ethanol; nickel; Hydrogenation;
With iron; acetic acid;
With hydrogenchloride; tin;
With hydrogenchloride; iron;
With phenylsilane; triphenylphosphine; iron(II) bromide; In toluene; at 110 ℃; for 16h; Inert atmosphere;
84 %Chromat.
With hydrazine hydrate; In tetrahydrofuran; at 100 ℃; for 10h; chemoselective reaction;
99 %Chromat.
With carbon monoxide; water; In tetrahydrofuran; at 125 ℃; for 24h; under 22502.3 - 45004.5 Torr; Inert atmosphere; Autoclave;
95 %Chromat.
With hydrogen; In tetrahydrofuran; water; at 120 ℃; for 4h; under 22502.3 Torr; chemoselective reaction;
5-bromo-1,2,3-trichloro-benzene
21928-51-8

5-bromo-1,2,3-trichloro-benzene

3,4,5-trichloroaniline
634-91-3

3,4,5-trichloroaniline

Conditions
Conditions Yield
5-bromo-1,2,3-trichloro-benzene; With magnesium; In tetrahydrofuran; Inert atmosphere;
With C10H17NO; In tetrahydrofuran; toluene; at -45 ℃; for 2h; Inert atmosphere;
With ammonium chloride; In tetrahydrofuran; water; toluene; Inert atmosphere;
47%

634-91-3 Upstream products

  • 20098-48-0
    20098-48-0

    3,4,5-trichloronitrobenzen

  • 21928-51-8
    21928-51-8

    5-bromo-1,2,3-trichloro-benzene

634-91-3 Downstream products

  • 33715-62-7
    33715-62-7

    N-(3,4,5-trichlorophenyl)acetamide

  • 35804-51-4
    35804-51-4

    1-(3,4,5-trichloro-phenyl)-biguanide; hydrochloride

  • 19010-53-8
    19010-53-8

    N -(3,4-dichloro-phenyl)-N '-(3,4,5-trichloro-phenyl)-urea

  • 609-19-8
    609-19-8

    3,4,5-trichlorophenol

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