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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)-

2-Pyridinecarboxylicacid, 6-[[(1,1-dimethylethoxy)carbonyl]amino]-

O=C(Nc1cccc(n1)C(=O)O)OC(C)(C)C Request for Quotation
Chemical Name: 2-Pyridinecarboxylicacid, 6-[[(1,1-dimethylethoxy)carbonyl]amino]-
CAS Number: 258497-21-1
Product Number: AG007NKX(AGN-PC-03TWQK)
Synonyms:
MDL No:
Molecular Formula: C11H14N2O4
Molecular Weight: 238.2399

Identification/Properties

Computed Properties
Molecular Weight:
238.243g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
238.095g/mol
Monoisotopic Mass:
238.095g/mol
Topological Polar Surface Area:
88.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
298
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-((tert-Butoxycarbonyl)amino)picolinic acid, also known as Boc-amino-picolinic acid, is a versatile compound widely used in chemical synthesis. This compound is a key building block in organic chemistry due to its ability to undergo various reactions and transformations, making it a valuable tool for the preparation of complex molecules.In chemical synthesis, 6-((tert-Butoxycarbonyl)amino)picolinic acid serves as a protecting group for the amino group. By attaching the Boc (tert-butoxycarbonyl) group to the amino group, the reactivity of the amine is masked, allowing selective reactions to take place elsewhere in the molecule without affecting the amine functionality. This protective group can be easily removed under mild conditions, enabling the synthesis of intricate organic compounds with controlled precision.Furthermore, 6-((tert-Butoxycarbonyl)amino)picolinic acid can also act as a chelating agent due to the presence of the picolinic acid moiety. This property makes it useful in coordination chemistry and metal complexation reactions, expanding its utility in the field of inorganic chemistry as well.Overall, the versatility and reactivity of 6-((tert-Butoxycarbonyl)amino)picolinic acid make it a valuable tool in chemical synthesis, enabling the efficient and selective construction of complex molecules for various applications in pharmaceuticals, materials science, and other disciplines of chemistry.