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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)-

tert-Butyl (3-hydroxypyridin-2-yl)carbamate

O=C(OC(C)(C)C)Nc1ncccc1O Request for Quotation
Chemical Name: tert-Butyl (3-hydroxypyridin-2-yl)carbamate
CAS Number: 902835-93-2
Product Number: AG00IG2I(AGN-PC-0WCRHM)
Synonyms:
MDL No:
Molecular Formula: C10H14N2O3
Molecular Weight: 210.2298

Identification/Properties

Computed Properties
Molecular Weight:
210.233g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
210.1g/mol
Monoisotopic Mass:
210.1g/mol
Topological Polar Surface Area:
71.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
225
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The product $name$ is a versatile compound widely used in chemical synthesis as a key building block. Its application in organic chemistry stems from its unique structural features, specifically the Boc-protected amino group and hydroxyl group on the pyridine ring.One of the primary uses of 2-(Boc-Amino)-3-hydroxypyridine is as a synthetic intermediate in the preparation of various pharmaceuticals and agrochemicals. The Boc (tert-butoxycarbonyl) protecting group on the amino function allows for selective manipulation of the amino group through a range of chemical reactions, including deprotection to expose the free amine for further functionalization or coupling with other molecules.The presence of the hydroxyl group on the pyridine ring also offers additional synthetic flexibility, enabling the compound to participate in various transformation reactions such as nucleophilic substitutions, cycloadditions, and metal-catalyzed cross-couplings. This enables the incorporation of the 2-(Boc-Amino)-3-hydroxypyridine moiety into complex molecular frameworks with precise control over regioselectivity and stereochemistry.Overall, the utility of 2-(Boc-Amino)-3-hydroxypyridine in chemical synthesis lies in its ability to serve as a multifunctional building block for the construction of diverse organic molecules, making it a valuable tool for researchers and chemists working in drug discovery, medicinal chemistry, and material science.