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  2. 1,2-Pyrrolidinedicarboxylic acid, 4-hydroxy-, 1-(1,1-dimethylethyl) ester,(2R,4R)-

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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-hydroxy-, 1-(1,1-dimethylethyl) ester,(2R,4R)-

O[C@H]1CN([C@H](C1)C(=O)O)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1,2-Pyrrolidinedicarboxylic acid, 4-hydroxy-, 1-(1,1-dimethylethyl) ester,(2R,4R)-
CAS Number: 135042-12-5
Product Number: AG00384A(AGN-PC-0PKHLT)
Synonyms:
MDL No: MFCD02094407
Molecular Formula: C10H17NO5
Molecular Weight: 231.2457

Identification/Properties

Computed Properties
Molecular Weight:
231.248g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
231.111g/mol
Monoisotopic Mass:
231.111g/mol
Topological Polar Surface Area:
87.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
296
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Boc-Cis-4-Hydroxy-D-Proline is a versatile compound widely used in chemical synthesis for its unique properties and applications. This compound serves as a key building block in the creation of peptide-based drugs, pharmaceuticals, and other bioactive molecules. With its Boc (tert-butyloxycarbonyl) protecting group, Boc-Cis-4-Hydroxy-D-Proline offers enhanced stability and reactivity during the synthesis process, allowing for precise control and manipulation of the molecule's structure. The incorporation of Boc-Cis-4-Hydroxy-D-Proline in peptide synthesis not only helps in the formation of peptide bonds but also plays a crucial role in modulating the conformation and biological activity of the resulting peptides. Additionally, this compound finds utility in the development of functionalized amino acids, peptide dendrimers, and peptidomimetics, adding a valuable tool to the toolbox of chemists and researchers working in the field of medicinal chemistry and drug discovery.