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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-Nitro-6-(trifluoromethyl)pyridine-2,4-diol

[O-][N+](=O)c1c(O)cc(nc1O)C(F)(F)F Request for Quotation
Chemical Name: 3-Nitro-6-(trifluoromethyl)pyridine-2,4-diol
CAS Number: 947144-26-5
Product Number: AG00IIGN(AGN-PC-0WAIGJ)
Synonyms:
MDL No:
Molecular Formula: C6H3F3N2O4
Molecular Weight: 224.0942

Identification/Properties

Computed Properties
Molecular Weight:
224.095g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
0
Exact Mass:
224.004g/mol
Monoisotopic Mass:
224.004g/mol
Topological Polar Surface Area:
95.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
390
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:
H302-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 3-Nitro-6-(trifluoromethyl)pyridine-2,4-diol plays a crucial role in chemical synthesis as a versatile building block. It is commonly used in the preparation of various pharmaceuticals, agrochemicals, and advanced materials due to its unique structural properties. Its presence of both nitro and hydroxyl groups allows for a range of functionalization reactions, enabling the synthesis of diverse compounds with enhanced biological activities or specific properties. Additionally, the trifluoromethyl group enhances the compound's lipophilicity and metabolic stability, making it favorable for drug design and development. In summary, 3-Nitro-6-(trifluoromethyl)pyridine-2,4-diol is a valuable component in chemical reactions for creating novel and impactful molecules across different industries.