106-52-5 | 4-Hydroxy-1-methylpiperidine

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$15.00	$10.00
100g	98%	in stock	$23.00	$16.00

Description

• Catalog Number: AB77603
• Chemical Name: 4-Hydroxy-1-methylpiperidine
• CAS Number: 106-52-5
• Molecular Formula: C6H13NO
• Molecular Weight: 115.17352
• MDL Number: MFCD00006500
• SMILES: CN1CCC(CC1)O
• NSC Number: 60705

Computed Properties

• Complexity: 66.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• XLogP3: 0.1

Upstream Synthesis Route

1-Methylpiperidin-4-ol, also known as N-methyl-4-piperidinol, is a versatile compound widely used in chemical synthesis. Its primary application lies in its role as a key building block in the creation of various pharmaceuticals and fine chemicals. 1-Methylpiperidin-4-ol's unique chemical structure and properties make it a valuable intermediate in the synthesis of diverse organic compounds. It serves as a crucial precursor in the production of pharmaceutical drugs, such as antihistamines, antipsychotics, and analgesics. Additionally, this compound is employed in the synthesis of specialty chemicals for industries ranging from cosmetics to agrochemicals.In chemical synthesis, 1-Methylpiperidin-4-ol acts as a versatile reagent, participating in a variety of reactions to form complex molecular structures. Its functional groups allow for selective derivatization, enabling chemists to tailor its properties for specific applications. Furthermore, the chirality of 1-Methylpiperidin-4-ol can be harnessed to create enantiomerically pure molecules, critical in drug development and material science.Overall, the strategic incorporation of 1-Methylpiperidin-4-ol in chemical synthesis processes demonstrates its significance as a foundational component in the creation of advanced compounds with diverse industrial applications.

Literature

• Characterisation of Plasmodium falciparum aspartic protease inhibition by piperidine derivatives.

  Natural product research 20111201

• Influence of structural variations in cationic and anionic moieties on the polarity of ionic liquids.

  The journal of physical chemistry. B 20110811

• Radiolabeled cholinesterase substrates: in vitro methods for determining structure-activity relationships and identification of a positron emission tomography radiopharmaceutical for in vivo measurement of butyrylcholinesterase activity.

  Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 20010201