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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)-

3-Pyridinecarboxylic acid, 5-(methylamino)-

CNc1cncc(c1)C(=O)O Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 5-(methylamino)-
CAS Number: 91702-88-4
Product Number: AG00345U(AGN-PC-0KBJQ5)
Synonyms:
MDL No: MFCD04971939
Molecular Formula: C7H8N2O2
Molecular Weight: 152.1506

Identification/Properties

Properties
BP:
378°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
152.153g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
152.059g/mol
Monoisotopic Mass:
152.059g/mol
Topological Polar Surface Area:
62.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
149
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(Methylamino)nicotinic acid, also known as MANA, is a versatile compound utilized in various chemical synthesis applications. This compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure contains a methylamino group on the nicotinic acid skeleton, offering specific reactivity and functionality for synthetic purposes.In chemical synthesis, 5-(Methylamino)nicotinic acid acts as a crucial building block for the preparation of bioactive molecules and complex organic substances. By incorporating MANA into a reaction pathway, chemists can access a diverse range of derivatives with modified properties and activities. This compound participates in numerous transformations, including amidation, esterification, and coupling reactions, enabling the construction of intricate molecular architectures.Furthermore, 5-(Methylamino)nicotinic acid plays a significant role in the development of novel compounds for medicinal and agricultural applications. Its presence as a core component in drug discovery and crop protection research underscores its importance in advancing the fields of healthcare and agriculture. By harnessing the synthetic potential of MANA, researchers can create tailored molecules with enhanced efficacy and specificity for targeted applications.Overall, the application of 5-(Methylamino)nicotinic acid in chemical synthesis showcases its versatility and utility as a valuable tool for the creation of innovative compounds with diverse functionalities and applications across various industries.