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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-(PHENYLSULFONYL)-5-INDOLEBORONIC ACID

OB(c1ccc2c(c1)ccn2S(=O)(=O)c1ccccc1)O Request for Quotation
Chemical Name: 1-(PHENYLSULFONYL)-5-INDOLEBORONIC ACID
CAS Number: 480438-51-5
Product Number: AG003BED(AGN-PC-0KKPDS)
Synonyms:
MDL No:
Molecular Formula: C14H12BNO4S
Molecular Weight: 301.1254

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
301.123g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
301.058g/mol
Monoisotopic Mass:
301.058g/mol
Topological Polar Surface Area:
87.9A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
458
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(1-(Phenylsulfonyl)-1H-indol-5-yl)boronic acid is a versatile chemical reagent widely used in organic synthesis. This compound serves as a valuable building block in the construction of complex organic molecules due to its boronic acid functionality, which can participate in a variety of important reactions.One of the key applications of (1-(Phenylsulfonyl)-1H-indol-5-yl)boronic acid is in Suzuki-Miyaura cross-coupling reactions. In this process, the boronic acid group on the compound reacts with an organoboron coupling partner in the presence of a palladium catalyst to form a new carbon-carbon bond. This reaction is highly useful for the synthesis of biaryl compounds, which are prevalent in pharmaceuticals, agrochemicals, and materials science.Furthermore, (1-(Phenylsulfonyl)-1H-indol-5-yl)boronic acid can also be employed in transition metal-catalyzed C-H activation reactions. By activating inert C-H bonds in organic molecules, this compound can facilitate the selective functionalization of complex substrates, enabling the synthesis of structurally diverse and intricate molecules.Overall, the unique reactivity and versatility of (1-(Phenylsulfonyl)-1H-indol-5-yl)boronic acid make it an indispensable tool for chemists engaged in the synthesis of novel organic compounds and the exploration of new chemical reactions.