| Identification | More | [Name]
N-Fmoc-8-Aminooctanoic acid | [CAS]
126631-93-4 | [Synonyms]
8-(FMOC-AMINO)CAPRYLIC ACID
8-(FMOC-AMINO)OCTANOIC ACID
FMOC-8-AMINOCAPRYLIC ACID
FMOC-8-AMINOOCTANOIC ACID
FMOC-8-AOC-OH
FMOC-AMINOCAPRYLIC ACID
FMOC-AOC(8)-OH
FMOC-NH-(CH2)7-COOH
N-(9-FLUORENYLMETHOXYCARBONYL)-8-AMINOCAPRYLIC ACID
N-(9-FLUORENYLMETHOXYCARBONYL)-8-AMINOOCTANOIC ACID
N-(9-FLUORENYLMETHYLOXYCARBONYL)-8-AMINO-OCTANOIC ACID
N-ALPHA-FMOC-8-AMINOOCTANOIC ACID
N-FMOC-8-AMINOOCTANOIC ACID
RARECHEM EM WB 0026
NALPHA-9-Fluorenylmethoxycarbonyl-8-aminooctanoic acid
Fmoc-omega-aminocaprylic acid
Fmoc-8-aminooctanoic acid (Fmoc-aminocaprylic acid)
8-Aminooctanoic acid, N-FMOC protected
8-(Fmoc-amino)caprylic acid, 8-(Fmoc-amino)octanoic acid
8-(9H-Fluoren-9-ylmethoxycarbonylamino)octanoic acid | [Molecular Formula]
C23H27NO4 | [MDL Number]
MFCD00235890 | [Molecular Weight]
381.46 | [MOL File]
126631-93-4.mol |
| Safety Data | Back Directory | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [HazardClass ]
IRRITANT | [HS Code ]
29242990 |
| Hazard Information | Back Directory | [Description]
N-Fmoc-8-aminooctanoic acid can be used as a PROTAC linker in the synthesis of PROTACs. N-Fmoc-8-aminooctanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. 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]
N-Fmoc-8-aminooctanoic acid can be used as a PROTAC linker in the synthesis of PROTACs. N-Fmoc-8-aminooctanoic acid is an alkane chain with terminal Fmoc-protected amine and carboxylic acid groups. 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. | [reaction suitability]
reaction type: Fmoc solid-phase peptide synthesis |
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