What is the (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID?

(4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is , while it's Molecular Formula is C 25 H 28 N 2 O 6 . Used in Pharmaceutical Research: (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is used as a key intermediate in the synthesis of pharmaceutical compounds, particularly for the development of new drugs. Its chiral nature and functional groups allow for the creation of enantioselective reactions and the formation of complex molecular structures with potential therapeutic applications. Used in Organic Synthesis: In the field of organic synthesis, (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID serves as a valuable building block for the construction of various organic molecules. Its cyclic oxazolidine ring and carboxylic acid group provide opportunities for further functionalization and the creation of diverse chemical entities with potential applications in materials science, agrochemicals, and other areas. Used in Chiral Chemistry: (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is utilized as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of enantiomerically pure compounds. Its presence can influence the stereochemistry of reactions, leading to the production of desired enantiomers with high selectivity, which is crucial for the development of enantioselective catalysts and chiral ligands. Used in Drug Development: In the drug development industry, (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is employed as a precursor for the synthesis of potential drug candidates. Its unique structure can be modified to incorporate various pharmacophores, leading to the discovery of new therapeutic agents with improved efficacy, selectivity, and safety profiles.

What is the CAS number for (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID?

The CAS number of (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is 252554-79-3.

What is (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID (252554-79-3) used for?

(4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is a chiral derivative of oxazolidine carboxylic acid, characterized by its molecular formula C18H27NO5 and a molecular weight of 333.41 g/mol. (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID features a 3-(FMOC-ALA) group attached to a cyclic oxazolidine ring, which is further complemented by a carboxylic acid functional group. Its unique structure and chirality make it a versatile building block in organic synthesis and pharmaceutical research, suitable for the development of novel compounds and drug molecules.

What is the (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID?

(4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is , while it's Molecular Formula is C 25 H 28 N 2 O 6 . Used in Pharmaceutical Research: (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is used as a key intermediate in the synthesis of pharmaceutical compounds, particularly for the development of new drugs. Its chiral nature and functional groups allow for the creation of enantioselective reactions and the formation of complex molecular structures with potential therapeutic applications. Used in Organic Synthesis: In the field of organic synthesis, (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID serves as a valuable building block for the construction of various organic molecules. Its cyclic oxazolidine ring and carboxylic acid group provide opportunities for further functionalization and the creation of diverse chemical entities with potential applications in materials science, agrochemicals, and other areas. Used in Chiral Chemistry: (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is utilized as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of enantiomerically pure compounds. Its presence can influence the stereochemistry of reactions, leading to the production of desired enantiomers with high selectivity, which is crucial for the development of enantioselective catalysts and chiral ligands. Used in Drug Development: In the drug development industry, (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is employed as a precursor for the synthesis of potential drug candidates. Its unique structure can be modified to incorporate various pharmacophores, leading to the discovery of new therapeutic agents with improved efficacy, selectivity, and safety profiles.

What is the CAS number for (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID?

The CAS number of (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is 252554-79-3.

What is (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID (252554-79-3) used for?

(4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID is a chiral derivative of oxazolidine carboxylic acid, characterized by its molecular formula C18H27NO5 and a molecular weight of 333.41 g/mol. (4S,5R)-3-(FMOC-ALA)-2,2,5-TRIMETHYL-OXAZOLIDINE-4-CARBOXYLIC ACID features a 3-(FMOC-ALA) group attached to a cyclic oxazolidine ring, which is further complemented by a carboxylic acid functional group. Its unique structure and chirality make it a versatile building block in organic synthesis and pharmaceutical research, suitable for the development of novel compounds and drug molecules.

Factory Sells Best Quality Fmoc-Ala-Thr[Psi(Me,Me)Pro]-OH 252554-79-3 with USP

Product Details;

CasNo： 252554-79-3

Molecular Formula： C25H28 N2 O6

Factory Sells Best Quality Fmoc-Ala-Thr[Psi(Me,Me)Pro]-OH 252554-79-3 with USP

Molecular Formula:C₂₅H₂₈N₂O₆
Molecular Weight:452.507
Boiling Point:681.2±55.0 °C(Predicted)
PKA:3.15±0.60(Predicted)
PSA：105.17000
Density:1.259±0.06 g/cm3(Predicted)
LogP:3.67900

252554-79-3Relevant academic research and scientific papers

Pseudo-Prolines in Peptide Synthesis: Direct Insertion of Serine and Threonine Derived Oxazolidines in Dipeptides

Woehr, Torsten,Mutter, Manfred

, p. 3847 - 3848 (1995)

Dipeptides containing serine and threonine derived oxazolidines are prepared by reacting side chain unprotected dipeptides containing C-terminal Thr or Ser with dimethoxypropane.The resulting building blocks can be coupled in Fmoc-based solid phase peptide synthesis enhancing peptide solvation by its secondary structure disrupting potential.The present procedure may be considered as a first step towards a reversible modification of structural and functional properties of bioactive peptides and proteins.

Solid phase synthesis of ω-aspartic thioacid containing peptides

Joseph, Ryan,Morales Padilla, Moises,Garner, Philip

supporting information, p. 4302 - 4304 (2015/06/22)

The Fmoc-based solid phase synthesis of unprotected ω-aspartic thioacid containing peptides is demonstrated. The method involves the novel use of a silyl ester as a carboxylate surrogate for mild peptide bond formation in the presence of a reactive ω-aspa

252554-79-3 Process route

: C₃₂H₃₄N₂O₆

: 252554-79-3
Fmoc-Ala-Thr(Ψ^Me,Mepro)-OH

Conditions

Conditions	Yield
With palladium 10% on activated carbon; hydrogen; In methanol; for 2h;	77%

: Fmoc-Ala-Thr(ox)-OAll

: 252554-79-3
Fmoc-Ala-Thr(Ψ^Me,Mepro)-OH

Conditions

Conditions	Yield

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Fmoc-Ala-Thr[Psi(Me,Me)Pro]-OH | CAS 252554-79-3

Product Details;

Factory Sells Best Quality Fmoc-Ala-Thr[Psi(Me,Me)Pro]-OH 252554-79-3 with USP

252554-79-3Relevant academic research and scientific papers

Pseudo-Prolines in Peptide Synthesis: Direct Insertion of Serine and Threonine Derived Oxazolidines in Dipeptides

Woehr, Torsten,Mutter, Manfred

, p. 3847 - 3848 (1995)

Solid phase synthesis of ω-aspartic thioacid containing peptides

Joseph, Ryan,Morales Padilla, Moises,Garner, Philip

supporting information, p. 4302 - 4304 (2015/06/22)

252554-79-3 Process route

Relevant Products