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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)-

(R)-2-(3,5-Difluorophenyl)pyrrolidine hydrochloride

Fc1cc(cc(c1)F)[C@H]1CCCN1.Cl Request for Quotation
Chemical Name: (R)-2-(3,5-Difluorophenyl)pyrrolidine hydrochloride
CAS Number: 1443538-50-8
Product Number: AG001JE4(AGN-PC-0WAMIX)
Synonyms:
MDL No: MFCD08751412
Molecular Formula: C10H12ClF2N
Molecular Weight: 219.6588

Identification/Properties

Computed Properties
Molecular Weight:
219.66g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
219.063g/mol
Monoisotopic Mass:
219.063g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
164
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H317
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of (R)-2-(3,5-Difluorophenyl)pyrrolidine hydrochloride in chemical synthesis lies in its utility as a chiral building block. This compound is employed as a key intermediate in the synthesis of various pharmaceuticals and fine chemicals. Due to its chiral nature, it serves as a crucial precursor for creating enantiopure compounds, which are essential in drug development and asymmetric synthesis. The hydrochloride form enhances the compound's stability and solubility, making it easier to handle and manipulate in synthetic processes. By incorporating (R)-2-(3,5-Difluorophenyl)pyrrolidine hydrochloride into chemical reactions, chemists can access enantioselective pathways to create complex molecules with high stereoselectivity, paving the way for the production of new drugs and bioactive compounds.