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CAS 84771-20-0

:

(2,5-dioxopyrrolidin-1-yl) 2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(1H-indol-3-yl)propanoate

Description:
The chemical substance known as (2,5-dioxopyrrolidin-1-yl) 2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(1H-indol-3-yl)propanoate, with the CAS number 84771-20-0, is a complex organic compound characterized by its unique structural features. It contains a pyrrolidine ring with two carbonyl groups, indicating the presence of a dioxo functionality, which contributes to its reactivity and potential as a building block in organic synthesis. The molecule also features a fluorenylmethoxycarbonyl (Fmoc) group, commonly used in peptide synthesis for protecting amino groups, and an indole moiety, which is known for its biological significance and aromatic properties. This compound is likely to exhibit solubility in organic solvents, and its stability may be influenced by the presence of the various functional groups. Its intricate structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or as intermediates in synthetic pathways. Overall, the compound's characteristics make it a subject of interest in both academic and industrial research settings.
Formula:C30H25N3O6
InChI:InChI=1/C30H25N3O6/c34-27-13-14-28(35)33(27)39-29(36)26(15-18-16-31-25-12-6-5-7-19(18)25)32-30(37)38-17-24-22-10-3-1-8-20(22)21-9-2-4-11-23(21)24/h1-12,16,24,26,31H,13-15,17H2,(H,32,37)
SMILES:c1ccc2c(c1)c1ccccc1C2COC(=NC(Cc1c[nH]c2ccccc12)C(=O)ON1C(=O)CCC1=O)O
Synonyms:
  • Fmoc-Trp-OSu
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Found 2 products.
  • Fmoc-Trp-Osu

    CAS:
    Formula:C30H25N3O6
    Molecular weight:523.5360

    Ref: IN-DA00G2YD

    ne
    To inquire
  • Nα-Fmoc-L-tryptophan N-hydroxysuccinimide ester

    CAS:
    <p>Nα-Fmoc-L-tryptophan N-hydroxysuccinimide ester is a chiral molecule that has a hydroxyl group and an amino group. It is used in the synthesis of peptides and proteins, as well as other organic compounds. The synthetic process of Nα-Fmoc-L-tryptophan N-hydroxysuccinimide ester can be divided into three steps: (1) the preparation of the Fmoc protected amino acid, (2) the coupling reaction with the amino acid to form a peptide bond, and (3) removal of the protecting group. This synthetic process is long acting because it is stable against hydrolysis by water.</p>
    Formula:C30H25N3O6
    Purity:Min. 95%
    Color and Shape:Powder
    Molecular weight:523.54 g/mol

    Ref: 3D-FN47783

    5g
    220.00€
    10g
    352.00€
    25g
    588.00€
    50g
    905.00€
    100g
    1,444.00€