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Ethyl-L-leucinathydrochlorid
H-Leu-OEt · L-LEUCINE ETHYL ESTER HYDROCHLORIDE · AI3-28816 · eucine ethyL · H-LEU-OET·HCL · H-LEU-OET HCL · L-Leu-OEt.HCL · H-L-Leu-OEt*HCl
Identifikatoren & physikalische Daten
| CAS No. | 2743-40-0 |
|---|---|
| Summenformel | C8H17NO2 |
| Durchschnittliche Molmasse | 159,23 g/mol |
| SMILES | CCOC(=O)C(N)CC(C)C |
| InChIKey | QIGLJVBIRIXQRN-UHFFFAOYSA-N |
| PubChem CID | 158178 |
| EC No. | 220-375-6 |
| Lokaler Name | Ethyl-L-leucinathydrochlorid |
Chemische & physikalische Eigenschaften
| XLogP | 1,3 |
|---|---|
| Polarare Oberfläche (TPSA) | 52,3 |
| H-Brücken-Donoren | 1 |
| H-Brücken-Akzeptoren | 3 |
| Frei drehbare Bindungen | 5 |
| Schwere Atome | 11 |
| Formalladung | 0 |
| Komplexität | 123 |
| Schmelzpunkt | 134-136 °C |
| Brechungsindex | 19 ° (C=5, EtOH) |
| Lagerbedingungen | Sealed in dry,Room Temperature |
| Aggregatzustand | Crystalline Powder |
| Farbe | White |
| Löslichkeit | Soluble in water. |
| BRN | 3994312 |
| InChI | InChI=1/C8H17NO2.ClH/c1-4-11-8(10)7(9)5-6(2)3/h6-7H,4-5,9H2,1-3H31H/t7-/s3 |
| InChIKey | NOUDPBCEONUCOV-WMASNCOMNA-N |
| SMILES | [C@H](N)(CC(C)C)C(=O)OCC.Cl |&1:0,r| |
| CAS Datenbank | 2743-40-0(CAS DataBase Reference) |
Sicherheit & Vorschriften
| GHS-Einstufung | WarningH315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory. |
|---|---|
| Regulatorische Informationen | L-Leucine, ethyl ester, hydrochloride: Does not have an individual approval but may be used under an appropriate group standard |
| Hazard Classes and Categories | Skin Irrit. 2 (100%) |
| Wassergefährdungsklasse (WGK) | 3 |
| Zollcode | 29224999 |
| Sicherheitshinweise (S) | 22-24/25 |
| Gefahrenklasse | IRRITANT |
Anwendungen & Verwendung
Verwenden
L-Leucine ethyl ester hydrochloride is used as an organic chemical synthesis intermediate.