This compound is an Fmoc-protected amino acid derivative, specifically this compound. It is used as a building block in peptide synthesis, where the Fmoc group provides temporary protection for the amino group.
نطاق المحتوى: تتعلق المعلومات الواردة في هذه الصفحة بتحديد المواد الكيميائية وبسياقات التوريد الصناعي والبحث والإنتاج. وهي لا تشكّل ادعاءً علاجياً أو نصيحة طبية أو إرشادات لاستخدام الأدوية.
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CAS 269078-75-3
3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)propanoic acid
Fmoc-protected amino acid building block
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyldec-9-enoic acid
Fmoc-protected amino acid building block
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-(1,3-dioxoisoindolin-2-yl)hexanoic acid
Fmoc-protected amino acid building block
(2R)-2-({[(9H-Fluoren-9-yl)methoxy]carbonyl}amino)-2-methyldec-9-enoic acid
Fmoc-protected amino acid building block
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
Pharmaceutical intermediate for boronic acid derivatives
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid
Pharmaceutical intermediate for boronic acid coupling
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
Pharmaceutical intermediate for borylation reactions
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-ol
Pharmaceutical intermediate for API synthesis
(4R)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-6-methylheptanoic acid
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CC(C)C[C@@H](CCC(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13