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  2. 3,5-Oxazolidinedicarboxylic acid, 2,2-dimethyl-4-phenyl-,3-(1,1-dimethylethyl) ester, (4S,5R)-

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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)-

3,5-Oxazolidinedicarboxylic acid, 2,2-dimethyl-4-phenyl-,3-(1,1-dimethylethyl) ester, (4S,5R)-

O=C(N1[C@@H](c2ccccc2)[C@@H](OC1(C)C)C(=O)O)OC(C)(C)C Request for Quotation
Chemical Name: 3,5-Oxazolidinedicarboxylic acid, 2,2-dimethyl-4-phenyl-,3-(1,1-dimethylethyl) ester, (4S,5R)-
CAS Number: 143527-70-2
Product Number: AG00383J(AGN-PC-0PU5KN)
Synonyms:
MDL No:
Molecular Formula: C17H23NO5
Molecular Weight: 321.3682

Identification/Properties

Computed Properties
Molecular Weight:
321.373g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
321.158g/mol
Monoisotopic Mass:
321.158g/mol
Topological Polar Surface Area:
76.1A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
462
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


The compound (4S,5R)-3-(tert-Butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic Acid, referred to as $name$, is a versatile reagent widely utilized in modern chemical synthesis. This compound plays a crucial role as a chiral building block in organic chemistry, particularly in the construction of complex molecules with high stereochemical purity.One of the primary applications of (4S,5R)-3-(tert-Butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic Acid is in asymmetric synthesis, where its unique stereochemistry enables precise control over the formation of chiral centers in target molecules. This compound can be employed in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals where chirality is of paramount importance for biological activity and efficacy.Furthermore, (4S,5R)-3-(tert-Butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic Acid serves as a versatile intermediate in the preparation of various natural products and functionalized compounds. Its ability to participate in a wide range of chemical transformations, such as C-C bond formation, functional group interconversion, and ring-closure reactions, makes it an invaluable tool for synthetic chemists striving to access complex molecular architectures efficiently.In summary, the utility of (4S,5R)-3-(tert-Butoxycarbonyl)-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic Acid in chemical synthesis lies in its strategic importance as a chiral scaffold for the construction of diverse molecules with controlled stereochemistry and functional group diversity. Its versatility and reliability make it an indispensable component in the toolbox of synthetic organic chemists seeking to address the challenges of modern molecule design and synthesis.