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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)-

1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

CC1(C)OB(OC1(C)C)c1cnn(c1)c1ccccc1 Request for Quotation
Chemical Name: 1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
CAS Number: 1002334-12-4
Product Number: AG0001AL(AGN-PC-0BL851)
Synonyms:
MDL No:
Molecular Formula: C15H19BN2O2
Molecular Weight: 270.1346

Identification/Properties

Computed Properties
Molecular Weight:
270.139g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
270.154g/mol
Monoisotopic Mass:
270.154g/mol
Topological Polar Surface Area:
36.3A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
340
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


1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole is a versatile compound that finds extensive application in chemical synthesis. This compound serves as a valuable building block in organic chemistry due to its unique structural properties and reactivity.In chemical synthesis, 1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole acts as a key intermediate for the construction of various organic molecules. Its boron functionality allows for selective cross-coupling reactions, particularly in palladium-catalyzed coupling reactions. This compound serves as a convenient source of phenylpyrazole moieties in the synthesis of biologically active compounds, pharmaceuticals, agrochemicals, and materials.Furthermore, the presence of the dioxaborolane group enhances the stability and reactivity of this compound, making it a valuable component in modern organic synthesis strategies. By incorporating 1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole into synthetic routes, chemists can access diverse chemical space and efficiently construct complex molecular architectures.Overall, the strategic utilization of 1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole in chemical synthesis enables the rapid and controlled assembly of multifunctional organic compounds with tailored properties and functionalities.