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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)-

5-Amino-2-(trifluoromethyl)pyridin-4-ol

Nc1cnc(cc1O)C(F)(F)F Request for Quotation
Chemical Name: 5-Amino-2-(trifluoromethyl)pyridin-4-ol
CAS Number: 1196153-82-8
Product Number: AG000PB2(AGN-PC-0WAGQC)
Synonyms:
MDL No:
Molecular Formula: C6H5F3N2O
Molecular Weight: 178.1119

Identification/Properties

Computed Properties
Molecular Weight:
178.114g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
0
Exact Mass:
178.035g/mol
Monoisotopic Mass:
178.035g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
277
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-Amino-2-(trifluoromethyl)pyridin-4-ol, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this molecule serves as a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its trifluoromethyl group offers enhanced chemical stability and lipophilicity, making it an attractive candidate for drug discovery and development.One of the key applications of 5-Amino-2-(trifluoromethyl)pyridin-4-ol in chemical synthesis is as a precursor for the synthesis of heterocyclic compounds. By taking advantage of its amino and hydroxyl functional groups, chemists can efficiently introduce additional substituents and modifications to tailor the properties of the final product. The presence of the trifluoromethyl group further enhances the biological activity and pharmacokinetic profile of the resulting molecules, making them potential candidates for various therapeutic applications.Furthermore, 5-Amino-2-(trifluoromethyl)pyridin-4-ol can be utilized in cross-coupling reactions, nucleophilic additions, and other organic transformations to introduce structural diversity and complexity into organic molecules. Its versatility and ease of functionalization make it a valuable tool for synthetic chemists looking to access novel chemical space and develop innovative compounds with desired properties.In summary, the application of 5-Amino-2-(trifluoromethyl)pyridin-4-ol in chemical synthesis offers a wide range of opportunities for the creation of structurally diverse and functionally advanced compounds with potential applications in pharmaceuticals, agrochemicals, and materials science.