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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-(4-methylphenyl)sulfonylpyrrolo[2,3-b]pyridin-3-yl]boronic acid

Cc1ccc(cc1)S(=O)(=O)n1cc(c2c1nccc2)B(O)O Request for Quotation
Chemical Name: [1-(4-methylphenyl)sulfonylpyrrolo[2,3-b]pyridin-3-yl]boronic acid
CAS Number: 882562-39-2
Product Number: AG008AWF(AGN-PC-07HAWA)
Synonyms:
MDL No:
Molecular Formula: C14H13BN2O4S
Molecular Weight: 316.1400

Identification/Properties

Computed Properties
Molecular Weight:
316.138g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
316.069g/mol
Monoisotopic Mass:
316.069g/mol
Topological Polar Surface Area:
101A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
488
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


The (1-Tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)boronic acid, often referred to as $name$, is a versatile compound widely used in chemical synthesis. This boronic acid derivative serves as a valuable building block in organic chemistry due to its ability to participate in various important reactions.One of the primary applications of (1-Tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)boronic acid is in Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful tool for forming carbon-carbon bonds and is widely used in the synthesis of complex organic molecules. By utilizing $name$ in this reaction, chemists can introduce the (1-Tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl) functionality into target molecules with high efficiency.Furthermore, (1-Tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)boronic acid can also be employed in palladium-catalyzed coupling reactions, such as Heck and Stille reactions, allowing for the selective and controlled functionalization of organic molecules. Its versatile reactivity and compatibility with various reaction conditions make $name$ a valuable tool for synthetic chemists working in the field of organic synthesis.