CAS 123387-50-8
:1-BOC-4-METHYLPIPERIDINE
Description:
1-BOC-4-Methylpiperidine, with the CAS number 123387-50-8, is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The "1-BOC" designation indicates the presence of a tert-butyloxycarbonyl (BOC) protecting group at the nitrogen atom, which is commonly used in organic synthesis to temporarily protect amines. The "4-methyl" indicates a methyl group substitution at the fourth position of the piperidine ring. This compound is typically utilized in organic synthesis, particularly in the preparation of pharmaceuticals and other complex organic molecules. It exhibits properties typical of piperidine derivatives, such as basicity due to the nitrogen atom, and can participate in various chemical reactions, including nucleophilic substitutions and cyclizations. The presence of the BOC group enhances its stability and solubility in organic solvents, making it a valuable intermediate in synthetic chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C11H21NO2
InChI:InChI=1/C11H21NO2/c1-9-5-7-12(8-6-9)10(13)14-11(2,3)4/h9H,5-8H2,1-4H3
SMILES:CC1CCN(CC1)C(=O)OC(C)(C)C
Synonyms:- 4-Methyl-Piperidine-1-Carboxylic Acid Tert-Butyl Ester
- Tert-Butyl 4-Methylpiperidine-1-Carboxylate
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Found 4 products.
1-Piperidinecarboxylic acid, 4-methyl-, 1,1-dimethylethyl ester
CAS:Formula:C11H21NO2Purity:97%Color and Shape:LiquidMolecular weight:199.2899N-tert-Butyloxycarbonyl-4-methyl-2-piperidine
CAS:Controlled Product<p>Applications 1,4-Disubstituted piperidine derivative, used in the preparation of thrombin inhibitors.<br>References Hanessian, S. et al., Bioorg. Med. Chem. Lett., 19, 5429 (2009); Cossy, J. & Belotti, D., Bioorg. Med. Chem. Lett. 11, 1989 (2001)<br></p>Formula:C11H21NO2Color and Shape:NeatMolecular weight:199.29
