1072878-42-2

Basic information

• Product Name: (2S)-(-)-N-(4-hydroxy-4-methyl-6-phenylhex-2-yn-1-yl)-2-(3-pyridyl)piperidine
• Synonyms: (2S)-(-)-N-(4-hydroxy-4-methyl-6-phenylhex-2-yn-1-yl)-2-(3-pyridyl)piperidine
• CAS NO: 1072878-42-2
• Molecular Weight: 348.488
• Mol File: 1072878-42-2.mol

Chemical Properties

• CAS DataBase Reference: (2S)-(-)-N-(4-hydroxy-4-methyl-6-phenylhex-2-yn-1-yl)-2-(3-pyridyl)piperidine(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-(-)-N-(4-hydroxy-4-methyl-6-phenylhex-2-yn-1-yl)-2-(3-pyridyl)piperidine(1072878-42-2)
• EPA Substance Registry System: (2S)-(-)-N-(4-hydroxy-4-methyl-6-phenylhex-2-yn-1-yl)-2-(3-pyridyl)piperidine(1072878-42-2)

Safety Data

• Hazardous Substances Data: 1072878-42-2(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 67646-68-8 3-methyl-5-phenylpent-1-yne-3-ol 
• 494-52-0 Anabasine 

Relevant articles and documents

Synthesis of N-propargylanabasine derivatives by the mannich reaction

N-Propargylanabasine derivatives bearing various substituents at the carbon atom of the alkyne fragment were obtained by the reaction of anabasine hydrochloride with terminal alkynes and paraformaldehyde. The reaction proceeded with retention of the C(2) chiral center in anabasine fragment. The by-products of the reaction, including 1,3-diacetylene (the products of dimerization of alkynes) and conjugated vinylacetylenes (the rearrangement products of the Mannich adducts) were isolated and characterized.