CAS 144222-22-0
:1-Boc-4-(aminomethyl)-piperidine
Description:
1-Boc-4-(aminomethyl)-piperidine is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group for amines, indicating that the compound has a protected amine functionality. The presence of the aminomethyl group at the 4-position of the piperidine ring suggests that it can participate in various chemical reactions, particularly in the synthesis of more complex molecules. This compound is typically used in organic synthesis and medicinal chemistry, often serving as an intermediate in the preparation of pharmaceuticals or other bioactive compounds. Its solubility and reactivity can vary depending on the solvent and conditions used, and it may exhibit basic properties due to the nitrogen atom in the piperidine ring. Overall, 1-Boc-4-(aminomethyl)-piperidine is a versatile building block in synthetic organic chemistry.
Formula:C11H22N2O2
InChI:InChI=1/C11H22N2O2/c1-10(2,3)15-9(14)13-7-5-11(4,12)6-8-13/h5-8,12H2,1-4H3
SMILES:CC(C)(C)OC(=O)N1CCC(C)(CC1)N
Synonyms:- 1-N-Boc-4-(aminomethyl)piperidine
- tert-Butyl 4-(aminomethyl)tetrahydropyridine-1(2H)-carboxylate
- Tert-Butyl 4-(Aminomethyl)Piperidine-1-Carboxylate
- [1-(Tert-Butoxycarbonyl)Piperidin-4-Yl]Methanaminium
- Tert-Butyl 4-Amino-4-Methylpiperidine-1-Carboxylate
- 4-Aminomethyl-1-Boc-piperidine
- 4-Aminomethyl-Piperidine-1-Carboxylic Acid Tert-Butyl Ester
- 1-Boc-4-aminomethyl-piperidine
- 1-Boc-4-(aminomethyl)piperidine
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Found 7 products.
4-(Aminomethyl)-1-tert-butoxycarbonylpiperidine
CAS:Formula:C11H22N2O2Purity:>98.0%(GC)(T)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:214.314-Aminomethyl-1-Boc-piperidine, 97%
CAS:<p>4-Aminomethyl-1-Boc-piperidine is used in the preparation biologically active compounds and orally active platelet-activating factor antagonists. It is used as an inhibitor for aspartic acid protease and Kinesin spindle protein. It is an active reactant involved in the enantioselective synthesis of</p>Formula:C11H23N2O2Purity:97%Color and Shape:Colorless, LiquidMolecular weight:215.32tert-butyl 4-(aminomethyl)piperidine-1-carboxylate
CAS:Formula:C11H22N2O2Purity:95%Color and Shape:SolidMolecular weight:214.30461-Boc-4-(aminomethyl)piperidine
CAS:Formula:C11H22N2O2Purity:≥ 98.0%Color and Shape:White to yellow solid or colourless to yellow liquidMolecular weight:214.304-(Aminomethyl)piperidine, N1-BOC protected
CAS:<p>4-(Aminomethyl)piperidine, N1-BOC protected</p>Formula:C11H22N2O2Purity:97%Color and Shape: white solidMolecular weight:214.30g/mol4-(Aminomethyl)-1-N-Boc-piperidine
CAS:Formula:C11H22N2O2Purity:95%Color and Shape:Liquid, ViscousMolecular weight:214.309N-Boc-4-(aminomethyl)piperidine
CAS:Controlled Product<p>Applications N-Boc-4-(aminomethyl)piperidine is a protected 4-substituted piperidinecarboxylate used in the preparation of orally active platelet-activating factor antagonists as well as other biologically active compounds.<br>References Carceller, E. et al.: J. Med. Chem., 39, 487 (1996);<br></p>Formula:C11H22N2O2Color and Shape:NeatMolecular weight:214.3






