| Identification | Back Directory | [Name]
FMOC-11-AMINOUNDECANOIC ACID | [CAS]
88574-07-6 | [Synonyms]
FMOC-11-AUN-OH
FMOC-NH-(CH2)10-COOH
FMOC-11-AMINOUNDECYLIC ACID
FMOC-11-AMINOUNDECANOIC ACID
11-(FMOC-AMINO)UNDECANOIC ACID
Fmoc-11-aminoundecanoic acid≥ 99% (HPLC)
N-(9-FLUORENYLMETHOXYCARBONYL)-11-AMINOUNDECYLIC ACID
N-(9-FLUORENYLMETHOXYCARBONYL)-11-AMINOUNDECANOIC ACID
11-(9H-fluoren-9-ylmethoxycarbonylamino)undecanoic acid
N-(9-FLUORENYLMETHYLOXYCARBONYL)-11-AMINO-UNDECANOIC ACID
NALPHA-9-Fluorenylmethoxycarbonyl-11-aminoundecanoic acid
Undecanoic acid,11-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]- | [Molecular Formula]
C26H33NO4 | [MDL Number]
MFCD00235891 | [MOL File]
88574-07-6.mol | [Molecular Weight]
423.54 |
| Chemical Properties | Back Directory | [storage temp. ]
2-8°C | [form ]
powder | [color ]
white | [BRN ]
4887890 | [Major Application]
peptide synthesis | [InChI]
1S/C26H33NO4/c28-25(29)17-7-5-3-1-2-4-6-12-18-27-26(30)31-19-24-22-15-10-8-13-20(22)21-14-9-11-16-23(21)24/h8-11,13-16,24H,1-7,12,17-19H2,(H,27,30)(H,28,29) | [InChIKey]
IMEVDILDSCXKJW-UHFFFAOYSA-N | [SMILES]
OC(=O)CCCCCCCCCCNC(=O)OCC1c2ccccc2-c3ccccc13 |
| Hazard Information | Back Directory | [Description]
Fmoc-11-aminoundecanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applicaitons. Fmoc-11-aminoundecanoic 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. | [Uses]
Fmoc-11-aminoundecanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applications. Fmoc-11-aminoundecanoic 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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| Company Name: |
Sigma-Aldrich
|
| Telephone: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
| Company Name: |
Shanghai GL Peptide Ltd.
|
| Telephone: |
+86-21-61263310 13764994101 |
| Website: |
www.chemicalbook.com/supplier/10480342/ |
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