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Home/Compounds/Research Reagent/Fmoc-D-proline
C20H19NO4
337.4 g/mol
Research ReagentWarning

N-(9-Fluorenylmethoxycarbonyl)-D-proline

CAS101555-62-8EC691-539-6
Category
Research Reagent
Compound Class
Peptide
Primary Use
Research Compound

N-(9-Fluorenylmethoxycarbonyl)-D-proline is an Fmoc-protected amino acid used as a building block in solid-phase peptide synthesis. Its structure incorporates a D-proline residue with a fluorenylmethoxycarbonyl (Fmoc) group, which facilitates controlled deprotection during peptide chain assembly.

Building block for Fmoc solid-phase peptide synthesisResearch reagent for peptide chemistry studies

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

StrongStructure SimilarSimilarity 0.91

Fmoc-Pro-Pro-OH

CAS129223-22-9

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StrongStructure SimilarSimilarity 0.91

Fmoc-Pro-Pro-Pro-OH

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SimilarStructure SimilarSimilarity 0.73

2-[[(2S)-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carbonyl]amino]acetic acid

CAS250695-65-9

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Fmoc-N-methyl-D-leucine

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Fmoc-L-tert-leucine

CAS132684-60-7

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N-Fmoc-L-Glutamine

CAS71989-20-3

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N-fmoc-L-norleucine

CAS77284-32-3

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ReferenceSame Category

Dihexyl (²H₄)benzene-1,2-dicarboxylate

CAS1015854-55-3

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Related Reading

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Safety Reference

Harmful
Harmful
Warning
H302Harmful if swallowed
H312Harmful in contact with skin
H315Causes skin irritation
H319Causes serious eye irritation
H332Harmful if inhaled
H335May cause respiratory irritation
Identifiers
IUPAC Name

(2R)-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carboxylic acid

InChIKey

ZPGDWQNBZYOZTI-GOSISDBHSA-N

SMILES

C1C[C@@H](N(C1)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C(=O)O

Synonyms (15)
  • (r)-n-fmoc-proline
  • D-Proline-N-Fmoc
  • FMOC-D-PRO
  • Fmoc-D-Pro-OH
  • Fmoc-D-proline
  • N-Fmoc-D-proline

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