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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)-

Boronic acid, [1-(triphenylmethyl)-1H-pyrazol-4-yl]-

OB(c1cnn(c1)C(c1ccccc1)(c1ccccc1)c1ccccc1)O Request for Quotation
Chemical Name: Boronic acid, [1-(triphenylmethyl)-1H-pyrazol-4-yl]-
CAS Number: 207307-51-5
Product Number: AG002IYX(AGN-PC-03JDJJ)
Synonyms:
MDL No:
Molecular Formula: C22H19BN2O2
Molecular Weight: 354.2095

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
354.216g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
354.154g/mol
Monoisotopic Mass:
354.154g/mol
Topological Polar Surface Area:
58.3A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
412
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(1-Trityl-1H-pyrazol-4-yl)boronic acid is a versatile and valuable reagent in chemical synthesis. It serves as a key building block in the construction of various organic molecules due to its ability to participate in Suzuki-Miyaura cross-coupling reactions. This compound is particularly useful in the formation of C-C bonds, a crucial step in the synthesis of pharmaceuticals, agrochemicals, and materials science. By acting as a boron reagent, (1-Trityl-1H-pyrazol-4-yl)boronic acid allows for the efficient and selective formation of carbon-carbon bonds under mild reaction conditions. Its application in organic synthesis enables chemists to access complex molecular structures in a predictable and controlled manner, making it an essential tool for modern synthetic chemistry.