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Thermo Scientific Chemicals
Ethyl (S)-(-)-1-Boc-4-oxopiperidine-2-carboxylate, 95%, Thermo Scientific Chemicals
| 產品號碼 | Quantity |
|---|---|
| H57213.03 亦稱為 H57213-03 | 1 g |
化學識別
CAS180854-44-8
IUPAC Name1-tert-butyl 2-ethyl 4-oxopiperidine-1,2-dicarboxylate
Molecular FormulaC13H21NO5
InChI KeyYAVQLRUBKDCOCI-UHFFFAOYNA-N
SMILESCCOC(=O)C1CC(=O)CCN1C(=O)OC(C)(C)C
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規格
規格表
規格表Assay (HPLC)≥94.0%
Proton NMRConforms
Infrared spectrumConforms
Appearance (Color)Pale yellow
FormLiquid.
1-Boc-4-oxopiperidine-2-carboxylate participates in the one-pot in situ formation and reaction of trimethyl (trichloromethyl) silane which finds application in the synthesis of 2, 2, 2-trichloromethylcarbinols.
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
1-Boc-4-oxopiperidine-2-carboxylate participates in the one-pot in situ formation and reaction of trimethyl (trichloromethyl) silane which finds application in the synthesis of 2, 2, 2-trichloromethylcarbinols.
Notes
Store in a cool ventilated place. Avoid strong oxidizing materials.
1-Boc-4-oxopiperidine-2-carboxylate participates in the one-pot in situ formation and reaction of trimethyl (trichloromethyl) silane which finds application in the synthesis of 2, 2, 2-trichloromethylcarbinols.
Notes
Store in a cool ventilated place. Avoid strong oxidizing materials.
RUO – Research Use Only
Kevin E. Henegar.; Ricardo Lira. One-Pot in Situ Formation and Reaction of Trimethyl(trichloromethyl)silane: Application to the Synthesis of 2,2,2-Trichloromethylcarbinols. J. Org. Chem. 2012, 77 (6),2999-3004.