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  2. 3-Chloro-2-(4-Morpholino)pyridine-4-boronic acid pinacol ester

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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-Chloro-2-(4-Morpholino)pyridine-4-boronic acid pinacol ester

Clc1c(nccc1B1OC(C(O1)(C)C)(C)C)N1CCOCC1 Request for Quotation
Chemical Name: 3-Chloro-2-(4-Morpholino)pyridine-4-boronic acid pinacol ester
CAS Number: 957198-28-6
Product Number: AG005YD4(AGN-PC-0W5C87)
Synonyms:
MDL No:
Molecular Formula: C15H22BClN2O3
Molecular Weight: 324.6108

Identification/Properties

Computed Properties
Molecular Weight:
324.612g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
324.141g/mol
Monoisotopic Mass:
324.141g/mol
Topological Polar Surface Area:
43.8A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
388
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


3-Chloro-2-(4-morpholino)pyridine-4-boronic acid pinacol ester, also known as $name$, serves as a versatile building block in chemical synthesis. This compound is commonly employed in organic reactions as a key reagent due to its unique structural properties.One of the primary applications of $name$ lies in its role as a valuable coupling agent in Suzuki-Miyaura cross-coupling reactions. This reaction, catalyzed by palladium, enables the formation of carbon-carbon bonds between an aryl halide and an organoboron compound. $name$ acts as the boronic acid component in this process, facilitating the coupling of diverse aryl halides with excellent efficiency and selectivity.Furthermore, $name$ is utilized in the synthesis of pharmaceutical intermediates and functional materials. Its specific chemical structure imparts stability and compatibility in various reaction conditions, making it an indispensable tool in the construction of complex molecular frameworks.In summary, the strategic incorporation of 3-Chloro-2-(4-morpholino)pyridine-4-boronic acid pinacol ester in chemical synthesis enables efficient access to a wide range of organic compounds and facilitates the discovery of novel molecules with diverse applications.