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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzenamine, 2,3,5-trichloro-

Clc1cc(N)c(c(c1)Cl)Cl Request for Quotation
Chemical Name: Benzenamine, 2,3,5-trichloro-
CAS Number: 18487-39-3
Product Number: AG003FF4(AGN-PC-0JLWY7)
Synonyms:
MDL No:
Molecular Formula: C6H4Cl3N
Molecular Weight: 196.4617

Identification/Properties

Properties
MP:
69 - 71°C
BP:
286°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
196.455g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
194.941g/mol
Monoisotopic Mass:
194.941g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
120
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3,5-Trichloroaniline is a versatile compound commonly used in chemical synthesis for its unique properties. This compound plays a crucial role in various reactions and processes due to its reactivity and chemical structure. In chemical synthesis, 2,3,5-Trichloroaniline is often employed as a building block or intermediate for the synthesis of complex molecules. Its trichloro substituents make it a valuable starting material for the introduction of other functional groups through substitution or addition reactions. One of the key applications of 2,3,5-Trichloroaniline is its utility in the preparation of dyes and pigments. By reacting with different reagents or coupling agents, this compound can be transformed into various colorful and stable compounds used in the textile and pigment industries. Additionally, 2,3,5-Trichloroaniline is also utilized in the synthesis of pharmaceuticals and agrochemicals. Its ability to undergo selective reactions at specific positions allows chemists to tailor its structure for specific biological activities or properties required in the development of new drugs or crop protection agents. Overall, the versatility and reactivity of 2,3,5-Trichloroaniline make it a valuable tool in chemical synthesis, enabling the creation of a wide range of compounds with diverse applications.