- Product Name 3,4,5-Trichloroaniline
- cas 634-91-3
- purity 99%
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
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-
20098-48-0
3,4,5-trichloronitrobenzen
-
-
634-91-3
3,4,5-trichloroaniline
| 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;
|
-
-
21928-51-8
5-bromo-1,2,3-trichloro-benzene
-
-
634-91-3
3,4,5-trichloroaniline
| 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
3,4,5-trichloronitrobenzen
-
21928-51-8
5-bromo-1,2,3-trichloro-benzene
634-91-3 Downstream products
-
33715-62-7
N-(3,4,5-trichlorophenyl)acetamide
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35804-51-4
1-(3,4,5-trichloro-phenyl)-biguanide; hydrochloride
-
19010-53-8
N -(3,4-dichloro-phenyl)-N '-(3,4,5-trichloro-phenyl)-urea
-
609-19-8
3,4,5-trichlorophenol