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N-Anisoyl-4-piperidone, also known as ANPP, is a chemical compound that serves as a precursor in the synthesis of fentanyl and its analogs. It is not a controlled substance by itself, but due to its role in the production of illicit opioids, it has been classified as a Schedule II controlled substance in the United States. ANPP is closely monitored and regulated by law enforcement and regulatory agencies to prevent its diversion for illegal purposes.

91586-26-4

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91586-26-4 Usage

Uses

Used in Pharmaceutical Industry:
N-Anisoyl-4-piperidone is used as a precursor chemical for the synthesis of fentanyl, a powerful synthetic opioid. It plays a crucial role in the production process, enabling the creation of fentanyl and its analogs.
Used in Regulatory and Law Enforcement:
ANPP is used as a target for monitoring and regulation by law enforcement and regulatory agencies. Its classification as a Schedule II controlled substance in the United States highlights the need for strict control over its availability and distribution to prevent its diversion for illegal purposes and the potential for increased production and distribution of dangerous drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 91586-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,8 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91586-26:
(7*9)+(6*1)+(5*5)+(4*8)+(3*6)+(2*2)+(1*6)=154
154 % 10 = 4
So 91586-26-4 is a valid CAS Registry Number.

91586-26-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methoxybenzoyl)piperidin-4-one

1.2 Other means of identification

Product number -
Other names N-ANISOYL-4-PIPERIDONE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:91586-26-4 SDS

91586-26-4Relevant academic research and scientific papers

Tankyrase inhibitor

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Paragraph 0238; 0242-0244, (2018/02/04)

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.

NOVEL ANALGESIC THAT BINDS FILAMIN A

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Page/Page column 30-31, (2010/12/29)

A compound, composition and method are disclosed that can provide analgesia. A contemplated compound has a structure that corresponds to Formula I, wherein R1 and R2 are substituents, and n, W, X and Y are defined within.

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

Boger, Dale B.,Mullican, Michael D.

, p. 4033 - 4044 (2007/10/02)

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.

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