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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-chloro-2-methoxypyridin-3-amine

COc1nc(Cl)ccc1N Request for Quotation
Chemical Name: 6-chloro-2-methoxypyridin-3-amine
CAS Number: 914222-86-9
Product Number: AG006B16(AGN-PC-09RUCG)
Synonyms:
MDL No:
Molecular Formula: C6H7ClN2O
Molecular Weight: 158.5856

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
158.585g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
158.025g/mol
Monoisotopic Mass:
158.025g/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-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


6-Chloro-2-methoxypyridin-3-amine is a valuable compound that finds versatile applications in chemical synthesis. This compound serves as a key building block in the development of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure allows it to participate in a range of synthetic reactions, making it a valuable tool for chemists working in drug discovery, materials science, and other fields. By incorporating 6-Chloro-2-methoxypyridin-3-amine into organic molecules, researchers can manipulate its chemical properties to create novel compounds with desired functionalities. Whether used as a starting material, intermediate, or reactive component, this compound plays a crucial role in expanding the synthetic toolkit available to chemists.