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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-phenylmethoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

CC1(C)OB(OC1(C)C)c1cncc(c1)OCc1ccccc1 Request for Quotation
Chemical Name: 3-phenylmethoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
CAS Number: 1375302-99-0
Product Number: AG0013IG(AGN-PC-0J57AK)
Synonyms:
MDL No:
Molecular Formula: C18H22BNO3
Molecular Weight: 311.1832

Identification/Properties

Computed Properties
Molecular Weight:
311.188g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
311.169g/mol
Monoisotopic Mass:
311.169g/mol
Topological Polar Surface Area:
40.6A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
380
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The Pyridine, 3-(phenylmethoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- compound has found significant application in chemical synthesis processes. Its unique structure and properties make it a valuable reagent in various organic transformations.This compound is often utilized as a building block in the synthesis of complex molecules due to its ability to participate in important reactions such as cross-coupling reactions. It serves as a key component in the formation of pharmaceuticals, agrochemicals, and advanced materials.In particular, the boron-containing moiety in the molecule enables selective transformations through Suzuki-Miyaura cross-coupling reactions. This versatile reaction allows for the creation of carbon-carbon bonds under mild conditions, making it an essential tool in modern synthetic chemistry.Overall, the Pyridine, 3-(phenylmethoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- compound plays a vital role in enabling the efficient synthesis of diverse organic compounds with applications ranging from drug discovery to material science.