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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-(4-chlorophenoxy)-

Clc1ccc(cc1)Oc1ccccc1N Request for Quotation
Chemical Name: Benzenamine, 2-(4-chlorophenoxy)-
CAS Number: 2770-11-8
Product Number: AG002UIJ(AGN-PC-0JLPQG)
Synonyms:
MDL No:
Molecular Formula: C12H10ClNO
Molecular Weight: 219.6669

Identification/Properties

Properties
BP:
321.0±22.0°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
219.668g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
219.045g/mol
Monoisotopic Mass:
219.045g/mol
Topological Polar Surface Area:
35.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
192
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-(4-Chlorophenoxy)aniline is an essential building block in chemical synthesis, commonly employed for various applications in organic chemistry. This compound serves as a versatile intermediate in the production of pharmaceuticals, agrochemicals, and dyes due to its unique structural qualities. Its chlorophenyl and aniline functional groups enable it to participate in a wide range of chemical reactions, facilitating the creation of complex molecules efficiently. In particular, 2-(4-Chlorophenoxy)aniline is frequently utilized in the synthesis of biologically active compounds and specialty chemicals, showcasing its significance in the field of organic chemistry. Its strategic positioning as a key intermediate highlights its utility and versatility in enabling the creation of diverse compounds through precise chemical transformations.