91586-26-4

Basic information

• Product Name: N-Anisoyl-4-piperidone
• Synonyms: N-Anisoyl-4-piperidone;1-(4-Methoxybenzoyl)-4-piperidinone
• CAS NO: 91586-26-4
• Molecular Formula: C₁₃H₁₅NO₃
• Molecular Weight: 233.26
• Mol File: 91586-26-4.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-Anisoyl-4-piperidone(CAS DataBase Reference)
• NIST Chemistry Reference: N-Anisoyl-4-piperidone(91586-26-4)
• EPA Substance Registry System: N-Anisoyl-4-piperidone(91586-26-4)

Safety Data

• Hazardous Substances Data: 91586-26-4(Hazardous Substances Data)

Usage

General Description

N-Anisoyl-4-piperidone, also known as ANPP, is a chemical compound that is commonly used in the production of fentanyl, a powerful synthetic opioid. ANPP itself is not a controlled substance, but its use in the illicit production of fentanyl has led to it being classified as a Schedule II controlled substance in the United States. ANPP is a precursor chemical for the synthesis of fentanyl and its analogs, and its availability has raised concerns about the potential for increased production and distribution of these dangerous drugs. Due to its role in the production of illicit opioids, ANPP is closely monitored and regulated by law enforcement and regulatory agencies to prevent its diversion for illegal purposes.

Upstream product

• 190012-08-9 1-(4-methoxybenzoyl)-4-piperidone ethylene ketal 
• 100-07-2 4-methoxy-benzoyl chloride 
• 177-11-7 4,4-ethylenedioxy-piperidine 
• 41979-39-9 4-piperidone hydrochloride 
• 41661-47-6 piperidin-4-one 

Downstream Products

• 91586-27-5 6-(4-Methoxy-benzoyl)-2-oxo-5,6,7,8-tetrahydro-2H-pyrano[3,2-c]pyridine-3-carboxylic acid methyl ester 
• 5056-80-4 (+/-)-sendaverine 
• 91586-44-6 7-Acetyl-6-methoxy-2-(4-methoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline 
• 91586-29-7 Methyl 6-methoxy-2-(4-methoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline-7-carboxylate 
• 91586-46-8 6-Methoxy-2-(4-methoxy-benzoyl)-1,2,3,4-tetrahydro-isoquinoline-7-carbonyl chloride 
• 91586-45-7 6-Methoxy-2-(4-methoxy-benzoyl)-1,2,3,4-tetrahydro-isoquinoline-7-carboxylic acid 
• 91586-47-9 7-Acetoxy-6-methoxy-2-(4-methoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline 
• 1224591-87-0 C₁₅H₂₀N₂O₃ 

Relevant articles and documents

Tankyrase inhibitor

The invention belongs to the technical field of medicine and specifically relates to a tankyrase inhibitor represented as a general formula (I) and pharmaceutically acceptable salts, esters, solvated compounds or stereisomers of the tankyrase inhibitor, wherein R1, R2, X1, X2, Y1, Y2, Y3, Y4, Z, L, n and A are defined as in the description. The invention also relates to preparation methods of the compounds, pharmaceutical preparations and pharmaceutical compositions containing the compounds, and applications of the compounds and the pharmaceutically acceptable salts, esters, solvated compounds or the stereoisomers of the compounds in preparing medicines of curing and/or preventing cancers and related diseases which are mediated by tankyrase.

Inverse Electron Demand Diels-Alder Reactions of 3-Carbomethoxy-2-pyrones. Controlled Introduction of Oxygenated Aromatics: Benzene, Phenol, Catechol, Resorcinol, and Pyrogallol Annulation. Regiospecific Total Synthesis of Sendaverine and a Preparation of 6,7-Benzomorphans

A full investigation of the preparation and Diels-Alder reactions of 3-carbomethoxy-2-pyrones is described.Methods for the preparation of a full range of oxygen-substituted aromatics: benzene, 1-, 2-, or 3-phenol, symmetrical or unsymmetrical o-catechol, resorcinol, and pyrogallol annulation from a common 3-carbomethoxy-2-pyrone intermediate are detailed.A regiospecific total synthesis of sendaverine, a 2-benzyltetrahydroisoquinoline possessing a selectively protected, symmetrical o-catechol, and a preparation of 6,7-benzomorphans are described.