1-[[2-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]pyrrolidine|1256360-38-9,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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-[[2-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]pyrrolidine

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Chemical Name:	1-[[2-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]pyrrolidine
CAS Number:	1256360-38-9
Product Number:	AG000O7H(AGN-PC-09PZNJ)
Synonyms:
MDL No:
Molecular Formula:	C17H25BFNO2
Molecular Weight:	305.1953

Identification/Properties
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Identification/Properties

Computed Properties

Molecular Weight:

305.2g/mol

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

305.196g/mol

Monoisotopic Mass:

305.196g/mol

Topological Polar Surface Area:

21.7A^2

Heavy Atom Count:

Formal Charge:

Complexity:

382

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

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Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

N/A

Signal Word:

UN#:

Hazard Statements:

Precautionary Statements:

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

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Chemical Structure

1-(2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)pyrrolidine is a versatile compound that finds application in chemical synthesis as a key building block in organic chemistry. Its unique structure containing both a pyrrolidine ring and a boronate ester moiety makes it a valuable reagent in various reactions.This compound's specific structure allows for its use in Suzuki-Miyaura cross-coupling reactions, a powerful tool in organic synthesis for forming carbon-carbon bonds. By utilizing the boronate ester functionality, 1-(2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)pyrrolidine can participate in these coupling reactions to introduce the desired aryl group onto different organic molecules selectively and efficiently.Furthermore, the presence of the pyrrolidine ring in the molecule can act as a chiral auxiliary, enabling asymmetric synthesis of molecules. This compound can serve as a useful starting material for the preparation of enantiomerically pure compounds by utilizing the chiral environment provided by the pyrrolidine moiety.Overall, the unique combination of the pyrrolidine ring and the boronate ester functionality in 1-(2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)pyrrolidine makes it a valuable tool for chemists engaged in advanced organic synthesis, enabling the efficient construction of complex molecules with precise control over stereochemistry and functional group positioning.