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Classification | Biochemical >> Amino acids and their derivatives >> Alanine derivatives |
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Name | N-[(Benzyloxy)Carbonyl]-L-Phenylalanyl-L-Alanine |
Synonyms | (2S)-2-{( |
Molecular Structure | ![]() |
Molecular Formula | C20H22N2O5 |
Molecular Weight | 370.40 |
CAS Registry Number | 21881-18-5 |
SMILES | C[C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)OCC2=CC=CC=C2 |
InChI | 1S/C20H22N2O5/c1-14(19(24)25)21-18(23)17(12-15-8-4-2-5-9-15)22-20(26)27-13-16-10-6-3-7-11-16/h2-11,14,17H,12-13H2,1H3,(H,21,23)(H,22,26)(H,24,25)/t14-,17-/m0/s1 |
InChIKey | LEJTXQOVOPDGHS-YOEHRIQHSA-N |
Density | 1.3±0.1g/cm3 (Cal.) |
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Boiling point | 666.1±55.0°C at 760 mmHg (Cal.) |
Flash point | 356.7±31.5°C (Cal.) |
Refractive index | 1.581 (Cal.) |
Safety Description | IRRITANT |
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SDS | Available |
(1) | Toshifumi Miyazawa, Eiichi Ensatsu, Makoto Hiramatsu, Ryoji Yanagihara and Takashi Yamada. a-Chymotrypsin-catalysed segment condensations via the kinetically controlled approach using carbamoylmethyl esters as acyl donors in organic media, J. Chem. Soc., Perkin Trans. 1, 2002, 0, 396. |
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Market Analysis Reports |
List of Reports Available for N-[(Benzyloxy)Carbonyl]-L-Phenylalanyl-L-Alanine |