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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-AMino-3-hydroxypyridine hydrochloride, 97%

Nc1ccncc1O.Cl Request for Quotation
Chemical Name: 4-AMino-3-hydroxypyridine hydrochloride, 97%
CAS Number: 1206679-69-7
Product Number: AG008WD2(AGN-PC-0WB2LX)
Synonyms:
MDL No:
Molecular Formula: C5H7ClN2O
Molecular Weight: 146.5749

Identification/Properties

Computed Properties
Molecular Weight:
146.57g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
146.02469g/mol
Monoisotopic Mass:
146.02469g/mol
Topological Polar Surface Area:
59.1Ų
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
76.8
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Aminopyridin-3-ol hydrochloride is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. As a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals, this compound plays a crucial role in the development of innovative materials and substances.In chemical synthesis, 4-Aminopyridin-3-ol hydrochloride serves as a valuable building block for the creation of complex organic molecules. Its high reactivity allows for efficient functional group transformations, enabling the synthesis of diverse compounds with specific properties and applications. This compound is particularly useful in the production of heterocyclic compounds, which are essential in drug discovery and development.Additionally, 4-Aminopyridin-3-ol hydrochloride is employed in the synthesis of bioactive compounds and specialty chemicals with potential applications in various industries. Its ability to participate in a wide range of chemical reactions makes it a versatile tool for chemists and researchers seeking to design and produce novel molecules with tailored functionalities.Overall, the application of 4-Aminopyridin-3-ol hydrochloride in chemical synthesis contributes to the advancement of pharmaceuticals, agrochemicals, and other important fields, offering new possibilities for the creation of innovative and impactful substances.