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  2. 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazolo[1,5-a]pyridine

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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-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazolo[1,5-a]pyridine

CC1(C)OB(OC1(C)C)c1cnn2c1cccc2 Request for Quotation
Chemical Name: 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazolo[1,5-a]pyridine
CAS Number: 1207557-48-9
Product Number: AG0092NN(AGN-PC-0CDA8Y)
Synonyms:
MDL No:
Molecular Formula: C13H17BN2O2
Molecular Weight: 244.0973

Identification/Properties

Computed Properties
Molecular Weight:
244.101g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
244.138g/mol
Monoisotopic Mass:
244.138g/mol
Topological Polar Surface Area:
35.8A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
319
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-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazolo[1,5-a]pyridine is a versatile compound widely used in chemical synthesis. It serves as a key building block in the construction of various organic molecules due to its unique reactivity and structural properties. In organic synthesis, this compound acts as a valuable heterocyclic scaffold, enabling the efficient formation of complex molecular structures. Its boron-containing moiety imparts specific reactivity, allowing for selective transformations and functional group manipulations in the synthesis of pharmaceuticals, agrochemicals, and materials. The pyrazole and pyridine rings in the molecule contribute to its diverse applications in the development of novel bioactive compounds and advanced materials. Through strategic incorporation into synthetic routes, 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazolo[1,5-a]pyridine facilitates the efficient assembly of target molecules with enhanced structural and chemical properties.