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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)-

3-(2-fluorophenyl)pyrrolidine;hydrochloride

Fc1ccccc1C1CNCC1.Cl Request for Quotation
Chemical Name: 3-(2-fluorophenyl)pyrrolidine;hydrochloride
CAS Number: 943843-62-7
Product Number: AG00II4G(AGN-PC-07A81Y)
Synonyms:
MDL No:
Molecular Formula: C10H13ClFN
Molecular Weight: 201.6683

Identification/Properties

Computed Properties
Molecular Weight:
201.669g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
201.072g/mol
Monoisotopic Mass:
201.072g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
149
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
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


The 3-(2-fluorophenyl)pyrrolidine hydrochloride compound is a valuable reagent frequently utilized in chemical synthesis processes. Its unique structure allows for a variety of applications in the creation of complex organic molecules. This compound is commonly employed as a building block for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. In particular, its incorporation into the design of drug molecules can enhance their biological activity and improve their overall efficacy. Additionally, the 3-(2-fluorophenyl)pyrrolidine hydrochloride can serve as a key intermediate in the preparation of diverse heterocyclic compounds with significant industrial and research implications. This versatile reagent plays a crucial role in enabling the development of novel compounds with specific functionalities, paving the way for advancements in various fields of chemistry.