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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)-

methyl 5-amino-2-methylpyridine-3-carboxylate

Cc1ncc(cc1C(=O)OC)N Request for Quotation
Chemical Name: methyl 5-amino-2-methylpyridine-3-carboxylate
CAS Number: 936130-28-8
Product Number: AG0061XG(AGN-PC-0DLR3C)
Synonyms:
MDL No:
Molecular Formula: C8H10N2O2
Molecular Weight: 166.1772

Identification/Properties

Computed Properties
Molecular Weight:
166.18g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
166.074g/mol
Monoisotopic Mass:
166.074g/mol
Topological Polar Surface Area:
65.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
172
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


Methyl 5-amino-2-methylnicotinate, also known as $name$, serves as a versatile building block in chemical synthesis. Due to its unique structure, this compound is widely used in organic chemistry for various applications. One of the primary roles of Methyl 5-amino-2-methylnicotinate in chemical synthesis is as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. The amino and methyl groups present in the molecule provide opportunities for functionalization and derivatization, allowing for tailored modifications to design specific target molecules. Furthermore, the nicotinate moiety imparts desirable properties and reactivity that are crucial for the efficient synthesis of intricate molecules. By incorporating Methyl 5-amino-2-methylnicotinate into synthetic routes, chemists can access diverse molecular frameworks and expedite the development of novel compounds with potential applications in various fields.