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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)-

(2S,4S)-4-Fluoropyrrolidine-2-carboxylic acid hydrochloride

OC(=O)[C@@H]1C[C@@H](CN1)F.Cl Request for Quotation
Chemical Name: (2S,4S)-4-Fluoropyrrolidine-2-carboxylic acid hydrochloride
CAS Number: 1001354-51-3
Product Number: AG00011Q(AGN-PC-0WAGEE)
Synonyms:
MDL No:
Molecular Formula: C5H9ClFNO2
Molecular Weight: 169.5819

Identification/Properties

Computed Properties
Molecular Weight:
169.58g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
169.031g/mol
Monoisotopic Mass:
169.031g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
128
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (2S,4S)-4-Fluoropyrrolidine-2-carboxylic acid hydrochloride is a versatile compound commonly used in chemical synthesis as a key building block in the creation of various pharmaceuticals and fine chemicals. Its chiral nature, with a specific stereochemistry at the 2nd and 4th positions, makes it valuable in the production of enantiomerically pure molecules.In chemical synthesis, this compound serves as a crucial intermediate for the preparation of biologically active compounds, such as potential drug candidates or agrochemicals. Due to its unique structure, (2S,4S)-4-Fluoropyrrolidine-2-carboxylic acid hydrochloride can participate in a wide range of reactions, enabling the introduction of the fluorine-containing pyrrolidine moiety into the target molecules.This compound's compatibility with various synthetic methodologies allows chemists to access diverse chemical space and develop innovative molecular structures with desirable properties. Its high purity and stereochemical integrity make it an ideal choice for researchers and synthetic chemists seeking to design and construct complex molecules with precision and efficiency.