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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)-

1,2-Pyrrolidinedicarboxylic acid, 4-fluoro-, 1-(1,1-dimethylethyl) ester,(2S,4R)-

F[C@@H]1C[C@H](N(C1)C(=O)OC(C)(C)C)C(=O)[O-] Request for Quotation
Chemical Name: 1,2-Pyrrolidinedicarboxylic acid, 4-fluoro-, 1-(1,1-dimethylethyl) ester,(2S,4R)-
CAS Number: 203866-14-2
Product Number: AG00295Q(AGN-PC-0QU1SZ)
Synonyms:
MDL No:
Molecular Formula: C10H15FNO4-
Molecular Weight: 232.2288

Identification/Properties

Properties
MP:
115-119 °C
BP:
346°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Refractive Index:
-69 ° (C=1, MeOH)
Computed Properties
Molecular Weight:
233.239g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
233.106g/mol
Monoisotopic Mass:
233.106g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
300
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (2S,4R)-1-(tert-Butoxycarbonyl)-4-fluoropyrrolidine-2-carboxylic acid is a versatile building block commonly used in chemical synthesis. Its unique structure and reactivity make it a valuable tool in organic chemistry for the preparation of various complex molecules.One important application of (2S,4R)-1-(tert-Butoxycarbonyl)-4-fluoropyrrolidine-2-carboxylic acid is as a chiral intermediate in the synthesis of pharmaceuticals and fine chemicals. Its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial in drug development where chirality can significantly impact the biological activity and safety of a molecule.This compound can undergo various chemical transformations, such as amine coupling, esterification, and cyclization reactions, to introduce different functional groups and scaffolds into a molecule. Its fluoro substituent can also serve as a useful handle for further derivatization or for enhancing the properties of the final product.Overall, (2S,4R)-1-(tert-Butoxycarbonyl)-4-fluoropyrrolidine-2-carboxylic acid is a valuable compound in chemical synthesis, particularly in the preparation of chiral molecules with potential applications in pharmaceuticals, agrochemicals, and materials science.