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Home/Compounds/Research Reagent/Fmoc-Leu-Thr(Psi(Me,Me)pro)-OH
C28H34N2O6
494.6 g/mol
Research Reagent

Fmoc-Leu-Thr(Psi(Me,Me)pro)-OH

CAS955048-89-2
Category
Research Reagent
Compound Class
Peptide
Primary Use
Research Compound

This compound is a protected amino acid derivative used as a building block in peptide synthesis. It features a fluorenylmethoxycarbonyl (Fmoc) protecting group and an oxazolidine ring system.

building block for peptide synthesisresearch reagent for coupling reactions

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Related Compounds

SimilarStructure SimilarSimilarity 0.81

4-Oxazolidinecarboxylic acid, 3-((2S)-2-(((9H-fluoren-9-ylmethoxy)carbonyl)amino)-1-oxo-3-phenylpropyl)-2,2,5-trimethyl-, (4S,5R)-

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SimilarStructure SimilarSimilarity 0.80

(4S,5R)-3-(Fmoc-Alaninyl)-2,2,5-trimethyloxazolidine-4-carboxylic acid

CAS252554-79-3

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SimilarStructure SimilarSimilarity 0.78

Fmoc-Val-Thr(Psi(Me,Me)pro)-OH

CAS168216-05-5

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SimilarStructure SimilarSimilarity 0.77

Fmoc-Ser(tBu)-Thr(Psi(Me,Me)pro)-OH

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ApplicationSame Use

Fmoc-Tyr(tBu)-Thr(Psi(Me,Me)pro)-OH

CAS920519-31-9

research compound

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(R)-A-METHYLLEUCINE

CAS29589-03-5

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4-[(Aminocarbonyl)amino]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-phenylalanine

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Boc-S-(4-methylbenzyl)-L-cysteine

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research compound

Related Reading

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Identifiers
IUPAC Name

(4S,5R)-3-[(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methylpentanoyl]-2,2,5-trimethyl-1,3-oxazolidine-4-carboxylic acid

InChIKey

OTDJFZHIGWFIEW-CQLNOVPUSA-N

SMILES

C[C@@H]1[C@H](N(C(O1)(C)C)C(=O)[C@H](CC(C)C)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C(=O)O

Synonyms (8)
  • Fmoc-Leu-Thr(|xMe,Mepro)-OH

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