1. Home
  2. Boronic acid, B-[2-(1-pyrrolidinylsulfonyl)phenyl]-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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, B-[2-(1-pyrrolidinylsulfonyl)phenyl]-

OB(c1ccccc1S(=O)(=O)N1CCCC1)O Request for Quotation
Chemical Name: Boronic acid, B-[2-(1-pyrrolidinylsulfonyl)phenyl]-
CAS Number: 913835-83-3
Product Number: AG006NKE(AGN-PC-07138D)
Synonyms:
MDL No: MFCD08689515
Molecular Formula: C10H14BNO4S
Molecular Weight: 255.0985

Identification/Properties

Properties
MP:
124-126
BP:
479.9°C/760mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
255.095g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
255.074g/mol
Monoisotopic Mass:
255.074g/mol
Topological Polar Surface Area:
86.2A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
348
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

Request for Quotation

Customer Feedback

Chemical Structure


Professional Grade Chemical: (2-(Pyrrolidin-1-ylsulfonyl)phenyl)boronic acidThis high-purity (2-(Pyrrolidin-1-ylsulfonyl)phenyl)boronic acid is a versatile chemical reagent commonly used in organic synthesis processes. Its unique structure and properties make it a valuable tool in various chemical reactions, particularly in the field of pharmaceutical research and development. In chemical synthesis, (2-(Pyrrolidin-1-ylsulfonyl)phenyl)boronic acid acts as a key building block for constructing complex molecules with specific functionalities. It plays a crucial role as a boronic acid derivative in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the formation of carbon-carbon bonds. This reagent is highly effective in facilitating the coupling of aryl or vinyl boronic acids with aryl halides or triflates, enabling the creation of novel compounds with diverse chemical properties.Furthermore, the presence of the pyrrolidine sulfonamide moiety in (2-(Pyrrolidin-1-ylsulfonyl)phenyl)boronic acid imparts additional stability and stereochemical control to the reaction process. This feature makes it a preferred choice in the synthesis of chiral molecules and biologically active compounds where precise stereochemistry is essential for their activity and selectivity.Overall, the application of (2-(Pyrrolidin-1-ylsulfonyl)phenyl)boronic acid in chemical synthesis offers a valuable tool for organic chemists and researchers seeking to efficiently and selectively construct complex molecular structures with tailored functionality for various applications.