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  2. 3-Pyridinecarboxylic acid,5-hydroxy-2-[[2-methyl-3-(trifluoromethyl)phenyl]amino]-

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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-hydroxy-2-[[2-methyl-3-(trifluoromethyl)phenyl]amino]-

Oc1cnc(c(c1)C(=O)O)Nc1cccc(c1C)C(F)(F)F Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid,5-hydroxy-2-[[2-methyl-3-(trifluoromethyl)phenyl]amino]-
CAS Number: 75369-61-8
Product Number: AG005Y03(AGN-PC-0U774P)
Synonyms:
MDL No:
Molecular Formula: C14H11F3N2O3
Molecular Weight: 312.2439

Identification/Properties

Properties
MP:
>150°C (dec.)
Storage:
-10 ℃;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
312.248g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
3
Exact Mass:
312.072g/mol
Monoisotopic Mass:
312.072g/mol
Topological Polar Surface Area:
82.4A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
405
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


5-Hydroxy-2-((2-methyl-3-(trifluoromethyl)phenyl)amino)nicotinic acid, also known as $name$, is a versatile compound widely used in chemical synthesis for its unique properties. This compound serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its structural characteristics make it a valuable intermediate in the production of various functional molecules.The presence of the hydroxyl group in 5-Hydroxy-2-((2-methyl-3-(trifluoromethyl)phenyl)amino)nicotinic acid enables it to participate in hydrogen bonding interactions, facilitating its use as a chiral auxiliary or a catalyst in asymmetric synthesis. Additionally, the nicotinic acid moiety provides a platform for derivatization, allowing for the introduction of different functional groups to tailor the molecule's properties.In chemical synthesis, 5-Hydroxy-2-((2-methyl-3-(trifluoromethyl)phenyl)amino)nicotinic acid can be employed as a starting material for the construction of complex organic molecules through various synthetic methodologies such as coupling reactions, functional group transformations, and cyclization reactions. Its ability to undergo diverse transformations makes it a valuable tool for organic chemists seeking to access novel compounds with desired properties.Overall, 5-Hydroxy-2-((2-methyl-3-(trifluoromethyl)phenyl)amino)nicotinic acid plays a crucial role in modern chemical synthesis by enabling the efficient and strategic construction of intricate molecular architectures for applications across different sectors of the chemical industry.