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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)-

3-Pyridinamine, 2,6-dimethoxy-, monohydrochloride

COc1ccc(c(n1)OC)N.Cl Request for Quotation
Chemical Name: 3-Pyridinamine, 2,6-dimethoxy-, monohydrochloride
CAS Number: 80789-72-6
Product Number: AG003IU8(AGN-PC-0UHU1S)
Synonyms:
MDL No:
Molecular Formula: C7H11ClN2O2
Molecular Weight: 190.6274

Identification/Properties

Properties
MP:
212 °C(lit.)
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
190.627g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
190.051g/mol
Monoisotopic Mass:
190.051g/mol
Topological Polar Surface Area:
57.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
121
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:
2
Compound Is Canonicalized:
Yes

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,6-Dimethoxypyridin-3-amine hydrochloride is a versatile compound extensively utilized in chemical synthesis as a key building block for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique chemical properties, this compound serves as a crucial intermediate in the synthesis of complex organic molecules. Its distinct structure enables it to participate in a wide range of reactions, including nucleophilic substitutions, condensations, and other transformations necessary for the construction of target molecules. With its significance in the field of chemical synthesis, 2,6-Dimethoxypyridin-3-amine hydrochloride plays a vital role in the development and production of innovative compounds with diverse applications.