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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-methoxypyridine-2,3-diamine;dihydrochloride

COc1ccc(c(n1)N)N.Cl.Cl Request for Quotation
Chemical Name: 6-methoxypyridine-2,3-diamine;dihydrochloride
CAS Number: 94166-62-8
Product Number: AG003B3Q(AGN-PC-0KO0HE)
Synonyms:
MDL No:
Molecular Formula: C6H11Cl2N3O
Molecular Weight: 212.0770

Identification/Properties

Properties
MP:
167-171℃
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
212.074g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
211.028g/mol
Monoisotopic Mass:
211.028g/mol
Topological Polar Surface Area:
74.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
109
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:
3
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-Methoxypyridine-2,3-diamine dihydrochloride is a versatile compound widely used in chemical synthesis for its unique properties. This compound is particularly valued for its ability to serve as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its presence in the molecular structure imparts specific desired properties, making it a valuable intermediate in the preparation of such compounds. Due to its selective reactivity and compatibility with a wide range of other chemical reagents, 6-Methoxypyridine-2,3-diamine dihydrochloride is commonly employed in the development of novel drug candidates, herbicides, and other biologically active molecules. Its use in chemical synthesis processes enables the efficient and precise construction of complex molecular architectures, facilitating the discovery and production of new materials with enhanced properties and functions.