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1-Boc-4-(aminomethyl)piperidine / 25 G

Purity: 97 %
Synonym: 1,1-Dimethylethyl 4-(aminomethyl)-1-piperidinecarboxylate, N-(tert-Butoxycarbonyl)-4-aminomethylpiperidine
Molecular Formula: C11H22N2O2
Molecular Weight: 214.30
SKU: MND-44932
CAS Number: 144222-22-0
MDL number: MFCD01076207
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 25 G  
707.00 EUR


Properties

Flash Point (C)No data available
Flash Point (F)No data available
Density1.013 g/mL at 25 °C (lit.)
Boiling Point237-238 °C (lit.)

 Product Description

1-BOC-4-(AMINOMETHYL)PIPERIDINE is a compound widely utilized in organic synthesis. Its versatile applications make it a valuable building block in the development of various pharmaceutical and chemical products.

 

Application:

Primarily employed as a crucial intermediate in organic synthesis, 1-BOC-4-(AMINOMETHYL)PIPERIDINE plays a key role in the manufacturing of pharmaceuticals and other chemical compounds.

 

 

Articles:

- Discovery of 2-(cyclopropanecarboxamido)-N-(5-((1-(4-fluorobenzyl)piperidin-4-yl)methoxy)pyridin-3-yl)isonicotinamide as a potent dual AChE/GSK3β inhibitor for the treatment of Alzheimer's disease: Significantly increasing the level of acetylcholine in the brain without affecting that in intestine

Publication Date: Available online 22 June 2021

Xueyang Jiang, Chang Liu, Manxing Zou, Huanfang Xie, Tailiang Lin, Weiping Lyu, Jian Xu, Yuan Li, Feng Feng, Haopeng Sun, Wenyuan Liu

https://doi.org/10.1016/j.ejmech.2021.113663

 

-Design and Synthesis of Specific Probes for Human 5-HT4 Receptor Dimerization Studies

Publication Date: September 8, 2005

Jean-Louis Soulier, Olivier Russo, Mireille Giner, Lucie Rivail, Magali Berthouze, Sandrine Ongeri, Bernard Maigret, Rodolphe Fischmeister, Frank Lezoualc'h, Sames Sicsic, and Isabelle Berque-Bestel

https://doi.org/10.1021/jm050234z

 

- Synthetic Hypotensive Agents. IV. dialkylaminoalkyl Esters of N-Methylnipecotic and N-Methylisonipecotic Acids and Some Bis-quaternary Ammonium Salts

Publication Date: May 1, 1956

Arthur P. Phillips

https://doi.org/10.1021/ja01590a044