| Identification | Back Directory | [Name]
FMOC-5-AMINOPENTANOIC ACID | [CAS]
123622-48-0 | [Synonyms]
FMOC-5-AVA-OH
FMOC-APE(5)-OH
RARECHEM EM WB 0074
FMOC-NH-(CH2)4-COOH
FMOC-5-AMINOVALERIC ACID
FMOC-5-AMINOPENTANOIC ACID
5-(FMOC-AMINO)VALERIC ACID
N-Fmoc-5-aminopentanoic acid
5-(FMOC-AMINO)PENTANOIC ACID
5-(Fmoc-amino)valericacid,98%
Fmoc-5-aminovaleric acid≥ 99% (HPLC)
FMoc-5-aMinopentanoic acid, tech grade
Fmoc-L-2-amino-5-phenylpentanoic acid DCHA
(9H-Fluoren-9-yl)MethOxy]Carbonyl 5-Ava-OH
Fmoc-5-aminopentanoic acid (Technical Grade)
N-(9-FLUORENYLMETHOXYCARBONYL)-5-AMINOVALERIC ACID
5-(9-FLUORENYLMETHYLOXYCARBONYL)AMINO-VALERIC ACID
N-(9-FLUORENYLMETHOXYCARBONYL)-5-AMINOPENTANOIC ACID
N-(9-FLUORENYLMETHYLOXYCARBONYL)-5-AMINO-PENTANOIC ACID
NALPHA-9-Fluorenylmethoxycarbonyl-5-aminopentanoic acid
5-(Fmoc-amino)pentanoic acid, 5-(Fmoc-amino)valeric acid
[(9H-fluoren-9-ylmethoxy)carbonyl] -5-amino- Pentanoic acid
5-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)pentanoic acid
Pentanoic acid, 5-[[(9H-fluoren-9-ylMethoxy)carbonyl]aMino]-
N-(9-Fluorenylmethyloxycarbonyl)-5-amino-pentanoic acid, 5-(9-Fluorenylmethyloxycarbonyl)amino-valeric acid | [Molecular Formula]
C20H21NO4 | [MDL Number]
MFCD00235889 | [MOL File]
123622-48-0.mol | [Molecular Weight]
339.39 |
| Chemical Properties | Back Directory | [Melting point ]
135-136 °C(Solv: ethyl ether (60-29-7); hexane (110-54-3)) | [Boiling point ]
575.8±33.0 °C(Predicted) | [density ]
1.232±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C
| [form ]
Powder | [pka]
4.71±0.10(Predicted) | [color ]
White | [BRN ]
3565625 | [InChI]
InChI=1S/C20H21NO4/c22-19(23)11-5-6-12-21-20(24)25-13-18-16-9-3-1-7-14(16)15-8-2-4-10-17(15)18/h1-4,7-10,18H,5-6,11-13H2,(H,21,24)(H,22,23) | [InChIKey]
ULLSWWGYZWBPHK-UHFFFAOYSA-N | [SMILES]
C(O)(=O)CCCCNC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O | [CAS DataBase Reference]
123622-48-0 |
| Hazard Information | Back Directory | [Description]
Fmoc-5-aminopentanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. | [Chemical Properties]
White powder | [Uses]
5-(Fmoc-amino)valeric acid is used as pharmaceutical intermediate. | [reaction suitability]
reaction type: Fmoc solid-phase peptide synthesis |
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