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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)-

4-bromo-2,6-dichloropyridin-3-amine

Clc1cc(Br)c(c(n1)Cl)N Request for Quotation
Chemical Name: 4-bromo-2,6-dichloropyridin-3-amine
CAS Number: 1121586-37-5
Product Number: AG00388F(AGN-PC-09RVAD)
Synonyms:
MDL No:
Molecular Formula: C5H3BrCl2N2
Molecular Weight: 241.9007

Identification/Properties

Computed Properties
Molecular Weight:
241.897g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
239.886g/mol
Monoisotopic Mass:
239.886g/mol
Topological Polar Surface Area:
38.9A^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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Bromo-2,6-dichloro-3-pyridinamine is a valuable chemical compound widely utilized in chemical synthesis due to its unique properties and versatile applications. In organic synthesis, this compound serves as an important building block for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its halogenated structure makes it a valuable intermediate in the production of complex organic molecules. Additionally, 4-Bromo-2,6-dichloro-3-pyridinamine is commonly employed in the development of novel materials and in medicinal chemistry research. Its ability to participate in a wide range of chemical reactions makes it a vital component in the synthesis of diverse compounds of industrial and scientific interest.