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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)-

6-bromo-3-methoxypyridin-2-amine

COc1ccc(nc1N)Br Request for Quotation
Chemical Name: 6-bromo-3-methoxypyridin-2-amine
CAS Number: 916737-77-4
Product Number: AG006EGZ(AGN-PC-0BWDYU)
Synonyms:
MDL No:
Molecular Formula: C6H7BrN2O
Molecular Weight: 203.0366

Identification/Properties

Properties
Storage:
Light sensitive;Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
203.039g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
201.974g/mol
Monoisotopic Mass:
201.974g/mol
Topological Polar Surface Area:
48.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
112
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Bromo-3-methoxy-2-pyridinamine is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound serves as an essential building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its bromo and methoxy functional groups make it an ideal candidate for further derivatization, allowing chemists to introduce additional substituents and manipulate the molecule's structure with precision. In organic synthesis, 6-Bromo-3-methoxy-2-pyridinamine can participate in a range of reactions such as cross-coupling, nucleophilic substitution, and transition metal-catalyzed transformations, enabling the formation of complex molecular architectures efficiently. This compound plays a crucial role in the development of novel compounds with diverse biological activities and may offer significant potential in drug discovery and material science applications.