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L-Valinamide hydrochloride - 98%, high purity , CAS No.3014-80-0
Basic Description
| Synonyms | AC-145 | CS-W013898 | M03135 | AS-15976 | L-valineamide hydrochloride | (s)-2-amino-3-methylbutyramide hydrochloride | MFCD00039085 | CS-W008135 | L-(+)-valinamide hydrochloride | L-Valinamide hydrochloride, 97% | SCHEMBL3201900 | N-(Boc)-L-Tyrosine methy |
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| Specifications & Purity | ≥98% |
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| Shipped In | Normal |
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| Product Description | Product Application:
It is a reagent used in the synthesis of alkylpyrazines. Also used in the synthesis of elastase inhibitory activity |
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Associated Targets(non-human)
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Names and Identifiers
| Pubchem Sid | 488198505 |
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| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488198505 |
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| IUPAC Name | (2S)-2-amino-3-methylbutanamide;hydrochloride |
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| INCHI | InChI=1S/C5H12N2O.ClH/c1-3(2)4(6)5(7)8;/h3-4H,6H2,1-2H3,(H2,7,8);1H/t4-;/m0./s1 |
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| InChi Key | XFCNYSGKNAWXFL-WCCKRBBISA-N |
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| Canonical SMILES | CC(C)C(C(=O)N)N.Cl |
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| Isomeric SMILES | CC(C)[C@@H](C(=O)N)N.Cl |
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| WGK Germany | 3 |
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| PubChem CID | 13689583 |
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| Molecular Weight | 152.62 |
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| Beilstein | 4(4)2662 |
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| Reaxy-Rn | 4198583 |
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Chemical and Physical Properties
| Solubility | Soluble in methanol (50 mg/ ml-clear, colorless solution). |
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| Specific Rotation[α] | 27 ° (C=1, H2O) |
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| Melt Point(°C) | 266-270°C |
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Safety and Hazards(GHS)
| WGK Germany | 3 |
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| Reaxy-Rn | 4198583 |
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References
| 1. Miki Hasegawa, Daichi Iwasawa, Takuma Kawaguchi, Hikaru Koike, Akira Saso, Shuhei Ogata, Ayumi Ishii, Hitomi Ohmagari, Munetaka Iwamura, Koichi Nozaki,. (2020-01-23) Chiroptical Spectroscopic Studies on Lanthanide Complexes with Valinamide Derivatives in Solution.. ChemPlusChem, 85 ((2)): ( 294-300 ). [PMID:31967409] |
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K2309562