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  2. Pyrrolidine,1-[[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]sulfonyl]-

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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)-

Pyrrolidine,1-[[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]sulfonyl]-

O=S(=O)(c1ccc(cc1)B1OC(C(O1)(C)C)(C)C)N1CCCC1 Request for Quotation
Chemical Name: Pyrrolidine,1-[[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]sulfonyl]-
CAS Number: 928657-21-0
Product Number: AG00IHD3(AGN-PC-0W1ZJ4)
Synonyms:
MDL No:
Molecular Formula: C16H24BNO4S
Molecular Weight: 337.2421

Identification/Properties

Computed Properties
Molecular Weight:
337.241g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
337.152g/mol
Monoisotopic Mass:
337.152g/mol
Topological Polar Surface Area:
64.2A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
513
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:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound $name$ is a highly versatile reagent commonly employed in chemical synthesis due to its unique chemical properties. It serves as a valuable building block in the creation of various organic molecules, particularly in the formation of C-C and C-N bonds. Utilized as a key intermediate in cross-coupling reactions, $name$ facilitates the introduction of the sulfonyl group into complex molecular structures, offering enhanced reactivity and stability. Through its strategic incorporation into synthetic pathways, this compound enables the efficient and precise assembly of functionalized pyrrolidine derivatives, thereby contributing to the advancement of pharmaceuticals, agrochemicals, and materials science.