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Thermo Scientific Chemicals
(S)-2-(Boc-amino)-4-phenylbutyric acid, 98%
CAS: 100564-78-1 | C15H21NO4 | 279.336 g/mol
化学物質識別子
CAS100564-78-1
IUPAC Name(2S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenylbutanoic acid
Molecular FormulaC15H21NO4
InChI KeyMCODLPJUFHPVQP-LBPRGKRZSA-N
SMILESCC(C)(C)OC(=O)N[C@@H](CCC1=CC=CC=C1)C(O)=O
さらに表示
スペックシート(S)-2-(Boc-amino)-4-phenylbutyric acid is used as organic chemical synthesis intermediate.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
(S)-2-(Boc-amino)-4-phenylbutyric acid is used as organic chemical synthesis intermediate.
Solubility
Soluble in methanol.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
(S)-2-(Boc-amino)-4-phenylbutyric acid is used as organic chemical synthesis intermediate.
Solubility
Soluble in methanol.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Hong-Yan Shen; Gui-Ling Tian; Yun-Hua Ye; Jianbo Wang. Non-coded amino acids as acyl donor substrates for peptide bond formation catalyzed by thermoase in toluene. Journal of Molecular Catalysis B: Enzymatic. 2005, 37, (1-6),26-29
- Jean-Christophe Califano; Laurent Goullieux; Muriel Amblard; Jean Alain Fehrentz; Nicole Bernad; Gilbert Berge; Jean Castel; Jean Martinez. Synthesis and biological activities of peptidomimetic analogues of compound A71623, a potent and selective CCK-A receptor agonist. Letters in Peptide Science. 1997, 4, (4),235-239