CAS 86060-90-4

1-(9H-Fluoren-9-ylmethyl) 2-(pentafluorophenyl) (2S)-1,2-pyrrolidinedicarboxylate

Description:

1-(9H-Fluoren-9-ylmethyl) 2-(pentafluorophenyl) (2S)-1,2-pyrrolidinedicarboxylate, with CAS number 86060-90-4, is a chemical compound characterized by its complex structure, which includes a pyrrolidine ring and multiple functional groups. The presence of the fluorenylmethyl group contributes to its aromatic properties, while the pentafluorophenyl moiety enhances its electron-withdrawing characteristics, potentially influencing its reactivity and solubility. This compound is likely to exhibit significant lipophilicity due to the large aromatic systems, which can affect its biological activity and interactions with other molecules. Additionally, the presence of two carboxylate groups suggests potential for hydrogen bonding and ionic interactions, which may play a role in its solubility in polar solvents. Overall, the unique combination of functional groups and structural features makes this compound of interest in various fields, including medicinal chemistry and materials science, where it may be explored for its potential applications in drug development or as a building block for more complex molecules.

Formula: C₂₆H₁₈F₅NO₄

InChI: InChI=1/C26H18F5NO4/c27-19-20(28)22(30)24(23(31)21(19)29)36-25(33)18-10-5-11-32(18)26(34)35-12-17-15-8-3-1-6-13(15)14-7-2-4-9-16(14)17/h1-4,6-9,17-18H,5,10-12H2/t18-/m0/s1

InChI key: InChIKey=CQBLOHXKGUNWRV-SFHVURJKSA-N

SMILES: C(OC(=O)N1[C@H](C(OC2=C(F)C(F)=C(F)C(F)=C2F)=O)CCC1)C3C=4C(C=5C3=CC=CC5)=CC=CC4

Synonyms:

• 1,2-Pyrrolidinedicarboxylic acid, 1-(9H-fluoren-9-ylmethyl) 2-(2,3,4,5,6-pentafluorophenyl) ester, (2S)-
• 1,2-Pyrrolidinedicarboxylic acid, 1-(9H-fluoren-9-ylmethyl) 2-(pentafluorophenyl) ester, (2S)-
• 1,2-Pyrrolidinedicarboxylic acid, 1-(9H-fluoren-9-ylmethyl) 2-(pentafluorophenyl) ester, (S)-
• 1-(9H-Fluoren-9-ylmethyl) 2-(pentafluorophenyl) (2S)-1,2-pyrrolidinedicarboxylate
• 1-(9H-Fluoren-9-ylmethyl) 2-(pentafluorophenyl) (2S)-pyrrolidine-1,2-dicarboxylate
• Fmoc-Pro-OPfp
• N-(Fluorenylmethoxycarbonyl)proline pentafluorophenyl ester
• N-9-Fluorenylmethoxycarbonyl-<span class="text-smallcaps">L</span>-proline pentafluorophenyl ester
• N-9-Fluorenylmethoxycarbonyl-L-proline pentafluorophenyl ester
• FMOC-PRO-OPFP USP/EP/BP
• N-(9-fluorenylmethoxycarbonyl)-L-proline pentafluorophenyl
• N-(9-fluorenylmethoxycarbonyl)-L-proline pentaflu
• Fmoc-L-proline pentafluorophenyl ester≥ 99% (HPLC)
• Fmoc-Pro-OP
• FMOC-PRO-OPFP 5 G
• (9H-Fluoren-9-yl)MethOxy]Carbonyl Pro-OPfp
• (S)-Fmoc-pyrrolidine-2-carboxylic acid pentafluorophenyl ester
• N-FMOC-L-PROLINE PENTAFLUOROPHENYL*ESTER
• N-(9-Fluorenylmethoxycarbonyl)-L-proline pentafluorophenyl ester,97%
• 1,2-Pyrrolidinedicarboxylicacid, 1-(9H-fluoren-9-ylmethyl) 2-(pentafluorophenyl) ester, (2S)-
• 86060-90-4
• N-ALPHA-FMOC-L-PROLINE PENTAFLUOROPHENYL ESTER
• NALPHA-9-Fluorenylmethoxycarbonyl-L-proline pentafluorophenyl ester
• N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-L-PROLINE PENTAFLUORPHENYL ESTER
• 1-(9H-fluoren-9-yl)methyl 2-(2,3,4,5,6-pentafluorophenyl) (2S)-pyrrolidine-1,2-dicarboxylate
• Fmoc-L-proline pentafluorophenyl ester, N-(9-Fluorenylmethoxycarbonyl)-L-proline pentafluorophenyl ester
• N-ALPHA-FMOC-L-PROLINE PENTAFLUOROPHENYL ESTER 98%
• FMOC-L-PROLINE PENTAFLUOROPHENYL ESTER
• FMOC-L-PRO-OPFP

Fmoc-Pro-OPfp

CAS: 86060-90-4

Bachem ID: 4011852.

Formula: C₂₆H₁₈F₅NO₄

Purity: 99.9%

Color and Shape: White

Molecular weight: 503.43

Ref: 01-4011852

Fmoc-Pro-OPfp

CAS: 86060-90-4

Formula: C₂₆H₁₈F₅NO₄

Purity: 98%

Molecular weight: 503.4174

Ref: IN-DA003QO1

Fmoc-Pro-OPfp

CAS: 86060-90-4

Fmoc-Pro-OPfp

Purity: 98%

Molecular weight: 503.42g/mol

Ref: 54-PC48008

Fmoc-Pro-OPfp

CAS: 86060-90-4

Formula: C₂₆H₁₈F₅NO₄

Purity: ≥ 95.0%

Color and Shape: White to off-white or pale yellow powder

Molecular weight: 503.42

Ref: 7W-GM6914

Fmoc-L-proline pentafluorophenyl ester

CAS: 86060-90-4

Fmoc-L-proline pentafluorophenyl ester is an estrogen analog that binds to the estrogen receptor α. It has been shown to inhibit cancer cell growth in vitro and in vivo. In addition, Fmoc-L-proline pentafluorophenyl ester inhibits the formation of new cancer cells by inducing cell death and inhibiting proliferation. This drug also has anti-inflammatory properties and is able to bind with calmodulin, which may be related to its ability to inhibit breast cancer cell growth.

Formula: C₂₆H₁₈F₅NO₄

Purity: Min. 95%

Molecular weight: 503.42 g/mol

Ref: 3D-FF47354

fmoc-pro-opfp

CAS: 86060-90-4

Formula: C₂₆H₁₈F₅NO₄

Purity: 98%(HPLC);RG

Molecular weight: 503.425

Ref: 10-F045500