| Description | Thiazolylalanine is an important raw material and intermediate. It is used in organic synthesis, pharmaceuticals, agrochemicals, and dyestuffs. |
| Synonyms | Thiazolylalanine, l, l-Thiazolylalanine |
| molecular weight | 172.2 |
| Molecular formula | C6H8N2O2S |
| CAS | 119433-80-6 |
| Storage | keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
| Solubility | DMSO: Soluble |
| References | 1. Mennen SM, Blank JT, Tran-Dubé MB, Imbriglio JE, Miller SJ. A peptide-catalyzed asymmetric Stetter reaction. Chem Commun (Camb). 2005 Jan 14;(2):195-7. Epub 2004 Nov 29. PubMed PMID: 15724183. 2. Mennen SM, Gipson JD, Kim YR, Miller SJ. Thiazolylalanine-derived catalysts for enantioselective intermolecular aldehyde-imine cross-couplings. J Am Chem Soc. 2005 Feb 16;127(6):1654-5. PubMed PMID: 15700996. 3. Heyl DL, Dandabathula M, Kurtz KR, Mousigian C. Opioid receptor binding requirements for the delta-selective peptide deltorphin. I: Phe3 replacement with ring-substituted and heterocyclic amino acids. J Med Chem. 1995 Mar 31;38(7):1242-6. PubMed PMID: 7707326. 4. Hashimoto N, Fujioka T, Hayashi K, Odaguchi K, Toyoda T, Nakamura M, Hirano K. Renin inhibitor: relationship between molecular structure and oral absorption. Pharm Res. 1994 Oct;11(10):1443-7. PubMed PMID: 7855049. |