This compound is a Fmoc-protected beta-amino acid derivative featuring a hydroxy and a benzyl substituent on the chiral backbone. It is primarily used as a building block in solid-phase peptide synthesis, enabling the incorporation of modified amino acid residues into peptide chains.
콘텐츠 범위: 이 페이지의 정보는 화학물질 식별 및 산업 공급·연구개발·제조 맥락을 대상으로 합니다. 치료 효능 주장, 의료 조언 또는 의약품 사용 지침에 해당하지 않습니다.
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CAS 1391586-46-1
(2R)-2-{[(9H-FLUOREN-9-YLMETHOXY)CARBONYL]AMINO}-4-METHYLPENTANOIC ACID
Peptide synthesis building block
Fmoc-3-Ala(2-thienyl)-OH
Peptide synthesis building block
Fmoc-Cys(pMeOBzl)-OH
Peptide synthesis building block
H-Glu-OtBu.HCl
Peptide synthesis building block
(2R,4S,5R)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2-(((dimethylamino)methylene)amino)-6-oxo-1H-purin-9(6H)-yl)-4-fluorotetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
Nucleoside phosphoramidite building block
Tert-butyl (5R)-5-amino-3,3-difluoropiperidine-1-carboxylate
pharmaceutical intermediate
Micafungin Impurity H
pharmaceutical impurity reference standard
(2S)-6-amino-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hexanoic acid hydrochloride
Fmoc-protected lysine for peptide synthesis
(2R,3R)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-2-hydroxy-4-phenylbutanoic acid
JZSULZSNDXGGHP-DHIUTWEWSA-N
C1=CC=C(C=C1)C[C@H]([C@H](C(=O)O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
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