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  2. 1H-Pyrrolo[2,3-b]pyridine, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

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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)-

1H-Pyrrolo[2,3-b]pyridine, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

CC1(C)OB(OC1(C)C)c1c[nH]c2c1cccn2 Request for Quotation
Chemical Name: 1H-Pyrrolo[2,3-b]pyridine, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS Number: 945256-29-1
Product Number: AG003ND5(AGN-PC-086E7B)
Synonyms:
MDL No:
Molecular Formula: C13H17BN2O2
Molecular Weight: 244.0973

Identification/Properties

Properties
BP:
405.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
244.101g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
244.138g/mol
Monoisotopic Mass:
244.138g/mol
Topological Polar Surface Area:
47.1A^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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Azaindole-3-boronic Acid Pinacol Ester serves as a valuable building block in chemical synthesis, particularly in the field of medicinal chemistry and material science. This compound is commonly used as a versatile reagent for the Suzuki-Miyaura cross-coupling reaction, facilitating the formation of carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and functional materials.Its boronic acid functionality enables selective and controlled reactions with various electrophiles, such as aryl halides and triflates, promoting the efficient construction of complex molecular structures. Additionally, the presence of the pinacol ester group enhances the compound's stability and compatibility in a wide range of reaction conditions, ensuring high yields and purity of the desired products.Furthermore, 7-Azaindole-3-boronic Acid Pinacol Ester exhibits excellent solubility in common organic solvents, which facilitates its incorporation into diverse synthetic strategies. Its unique chemical properties and reactivity make it a valuable tool for the design and synthesis of novel bioactive molecules and advanced materials with potential applications in drug discovery and materials science.