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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)-

N,N-dimethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

CN(S(=O)(=O)c1ccccc1B1OC(C(O1)(C)C)(C)C)C Request for Quotation
Chemical Name: N,N-dimethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide
CAS Number: 486422-06-4
Product Number: AG00DC53(AGN-PC-00YV25)
Synonyms:
MDL No:
Molecular Formula: C14H22BNO4S
Molecular Weight: 311.2048

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
311.203g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
311.136g/mol
Monoisotopic Mass:
311.136g/mol
Topological Polar Surface Area:
64.2A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
468
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:
H302
Precautionary Statements:
P264-P270-P301+P312-P330-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound N,N-Dimethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide is a versatile reagent in chemical synthesis. It is commonly used as a source of the boron functionality in various organic reactions. This compound can be employed in Suzuki-Miyaura cross-coupling reactions, where it acts as a boron source to facilitate the coupling of aryl halides or pseudohalides with organoboron reagents. Additionally, N,N-Dimethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide is utilized in the preparation of functionalized boron-containing compounds, which are valuable intermediates in the synthesis of pharmaceuticals, agrochemicals, and materials. Its unique structure and reactivity make it a useful tool for organic chemists seeking to introduce boron functionalities into their target molecules.