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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)-

2-Methoxy-3-(trifluoromethyl)pyridine-5-boronic Acid Pinacol Ester

COc1ncc(cc1C(F)(F)F)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 2-Methoxy-3-(trifluoromethyl)pyridine-5-boronic Acid Pinacol Ester
CAS Number: 1150561-61-7
Product Number: AG000FRR(AGN-PC-0WA6V7)
Synonyms:
MDL No:
Molecular Formula: C13H17BF3NO3
Molecular Weight: 303.0852

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
303.088g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
2
Exact Mass:
303.125g/mol
Monoisotopic Mass:
303.125g/mol
Topological Polar Surface Area:
40.6A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
373
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:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 2-Methoxy-3-(trifluoromethyl)pyridine-5-boronic Acid Pinacol Ester is a versatile and valuable chemical compound widely utilized in modern chemical synthesis processes. This compound serves as a key building block in the creation of various organic molecules and pharmaceutical intermediates.One of the primary applications of 2-Methoxy-3-(trifluoromethyl)pyridine-5-boronic Acid Pinacol Ester lies in its role as a powerful reagent for Suzuki-Miyaura cross-coupling reactions. This reaction, catalyzed by palladium, enables the formation of new carbon-carbon bonds between aryl or heteroaryl boronic acids and halides or pseudohalides. Through this process, complex molecular structures can be constructed with precision and efficiency.Additionally, this compound can be employed in the synthesis of diverse biologically active compounds, agrochemicals, and materials of interest to the pharmaceutical and chemical industries. Its unique structural features, including the trifluoromethyl and methoxy groups, contribute to its reactivity and compatibility with a wide range of synthetic transformations.In summary, the 2-Methoxy-3-(trifluoromethyl)pyridine-5-boronic Acid Pinacol Ester plays a crucial role in advanced chemical synthesis strategies, making it an indispensable tool for the development of novel molecules with potential applications in various fields.