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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-Trifluoromethyl-pyridin-2-yl) methanol

OCc1ncccc1C(F)(F)F Request for Quotation
Chemical Name: (3-Trifluoromethyl-pyridin-2-yl) methanol
CAS Number: 131747-44-9
Product Number: AG000ZN8(AGN-PC-0L0UBS)
Synonyms:
MDL No:
Molecular Formula: C7H6F3NO
Molecular Weight: 177.1238

Identification/Properties

Properties
BP:
201.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
177.126g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
177.04g/mol
Monoisotopic Mass:
177.04g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
148
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-H320-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Customer Feedback

Chemical Structure


(3-Trifluoromethylpyridin-2-yl)methanol, commonly referred to as $name$, is a versatile chemical compound that finds significant application in chemical synthesis. This compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique trifluoromethylpyridine moiety imparts valuable properties to the molecules it is incorporated into, enhancing their biological activity and stability.In organic synthesis, (3-Trifluoromethylpyridin-2-yl)methanol acts as a valuable starting material for the construction of complex molecules. It can undergo a range of chemical transformations, such as oxidation, reduction, and functional group interconversions, making it a crucial intermediate in the development of novel compounds. Additionally, the presence of the trifluoromethyl group enables selective reactions and enhances the overall efficiency of the synthesis process.Furthermore, (3-Trifluoromethylpyridin-2-yl)methanol is employed in the synthesis of fluorinated building blocks, which are in high demand for the development of fluorine-containing pharmaceuticals and materials. Its ability to introduce a trifluoromethyl group into organic molecules makes it a valuable tool for medicinal chemists and researchers working in drug discovery and development.Overall, the application of (3-Trifluoromethylpyridin-2-yl)methanol in chemical synthesis extends across various industries, contributing to the creation of new and innovative compounds with diverse applications.