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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)-

2-amino-6-bromo-4-chlorophenol

Clc1cc(N)c(c(c1)Br)O Request for Quotation
Chemical Name: 2-amino-6-bromo-4-chlorophenol
CAS Number: 179314-60-4
Product Number: AG019TVU(AG019TVU)
Synonyms:
MDL No:
Molecular Formula: C6H5BrClNO
Molecular Weight: 222.4670

Identification/Properties

Computed Properties
Molecular Weight:
222.466g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
220.924g/mol
Monoisotopic Mass:
220.924g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
124
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-Amino-6-bromo-4-chlorophenol, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure makes it a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and organic compounds. In chemical synthesis, $name$ is commonly used as a key starting material for the synthesis of complex molecules due to its functional groups that allow for strategic modifications. Its reactivity and compatibility with a wide range of other compounds make it an essential component in the creation of new and innovative chemical products. By incorporating 2-Amino-6-bromo-4-chlorophenol into a synthetic pathway, chemists can access a diverse array of derivatives with tailored properties for specific applications. Whether utilized in medicinal chemistry, materials science, or other fields, $name$ is prized for its versatility and utility in advancing the frontiers of chemical innovation.