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Home/Compounds/Research Reagent/Fmoc-Pro-Pro-OH
C25H26N2O5
434.5 g/mol
Research Reagent

N-alpha-(9-Fluorenylmethyloxycarbonyl)-L-prolinyl-L-proline

CAS129223-22-9EC846-642-2
Category
Research Reagent
Compound Class
Peptide
Primary Use
Research Compound

This compound is a research reagent used in peptide synthesis, specifically as a protected dipeptide building block. It consists of two proline residues with an Fmoc (fluorenylmethoxycarbonyl) protecting group and a free carboxylic acid, making it suitable for solid-phase peptide synthesis.

research compound for peptide synthesisFmoc-protected dipeptide building block for solid-phase peptide synthesis

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 1.00

Fmoc-Pro-Pro-Pro-OH

CAS134303-96-1

research compound

StrongStructure SimilarSimilarity 0.91

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

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pharmaceutical intermediate

StrongStructure SimilarSimilarity 0.91

Fmoc-D-proline

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research compound

ApplicationSame Use

Fmoc-Ala-Pro-OH

CAS186023-44-9

research compound

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N-[(tert-Butoxy)carbonyl]-L-tryptophan

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research compound

ApplicationSame Use

Fmoc-L-glutamic acid 5-allyl ester

CAS133464-46-7

research compound

ApplicationSame Use

Fmoc-Gln(Trt)-Thr(Psi(Me,Me)pro)-OH

CAS1572725-72-4

research compound

ReferenceSame Category

(R)-2-((R)-2-((R)-2-Acetamido-3-(naphthalen-2-yl)propanamido)-3-(4-chlorophenyl)propanamido)-3-(pyridin-3-yl)propanoic acid

CAS129225-22-5

research compound

Identifiers
IUPAC Name

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

InChIKey

VRAQFWSWKRNOGU-VXKWHMMOSA-N

SMILES

C1C[C@H](N(C1)C(=O)[C@@H]2CCCN2C(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35)C(=O)O

Synonyms (12)
  • Fmoc-L-Pro-L-Pro-OH
  • Fmoc-Pro-Pro
  • Fmoc-Pro-Pro-OH
  • N-Fmoc-L-prolyl-L-proline