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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-methoxy-5-[(2-methylpropan-2-yl)oxycarbonylamino]pyridine-4-carboxylic acid

COc1ncc(c(c1)C(=O)O)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: 2-methoxy-5-[(2-methylpropan-2-yl)oxycarbonylamino]pyridine-4-carboxylic acid
CAS Number: 183741-86-8
Product Number: AG003M7Y(AGN-PC-0KKPAQ)
Synonyms:
MDL No: MFCD07437869
Molecular Formula: C12H16N2O5
Molecular Weight: 268.2658

Identification/Properties

Properties
BP:
415°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
268.269g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
5
Exact Mass:
268.106g/mol
Monoisotopic Mass:
268.106g/mol
Topological Polar Surface Area:
97.8A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
340
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
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


5-((tert-Butoxycarbonyl)amino)-2-methoxyisonicotinic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is widely utilized in the field of organic chemistry due to its unique structural properties and reactivity. It serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, $name$ is frequently employed as a masked amino acid derivative for the protection of amine functionalities. By utilizing the tert-butoxycarbonyl (Boc) protecting group, the amine group in $name$ can be shielded from unwanted reactions, allowing for selective transformations at other reactive sites within a molecule. This protection-deprotection strategy enables chemists to control the sequence of reactions and facilitate the synthesis of complex molecules with improved yields and selectivity.Furthermore, the methoxy group present in $name$ can serve as a directing group for regioselective functionalization reactions. Through suitable manipulation of the methoxy functionality, chemists can direct subsequent chemical transformations to specific positions on the aromatic ring, leading to the formation of desired products with high efficiency.In summary, the application of 5-((tert-Butoxycarbonyl)amino)-2-methoxyisonicotinic acid in chemical synthesis offers a valuable tool for the construction of diverse molecular architectures with precision and versatility. Its strategic use as a building block in synthetic pathways contributes to the development of novel compounds with potential applications in various industries.