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1-Benzyl-3-methoxy-piperidin-4-one is a versatile chemical compound belonging to the class of piperidinones. It features a piperidinone ring with a benzyl group and a methoxy group attached, making it a valuable intermediate in the synthesis of pharmaceutical drugs and other organic compounds. Known for its potential biological and pharmacological activities, 1-Benzyl-3-methoxy-piperidin-4-one can interact with the central nervous system and has been studied for its potential use in treating various medical conditions. Its structure and properties make it a promising building block for the development of new compounds with therapeutic properties. However, it is crucial to handle and store this chemical with care due to its potential risks to human health and the environment if not properly managed.

134473-73-7

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134473-73-7 Usage

Uses

Used in Pharmaceutical Industry:
1-Benzyl-3-methoxy-piperidin-4-one is used as a key intermediate in the synthesis of pharmaceutical drugs for its potential biological and pharmacological activities. Its ability to interact with the central nervous system makes it a promising candidate for the development of new therapeutic agents.
Used in Organic Synthesis:
1-Benzyl-3-methoxy-piperidin-4-one is used as a versatile building block in organic synthesis for the creation of new compounds with potential therapeutic properties. Its unique structure allows for the development of innovative molecules with diverse applications in various fields.
Used in Research and Development:
1-Benzyl-3-methoxy-piperidin-4-one is used as a subject of research for its potential use in the treatment of various medical conditions. Scientists and researchers explore its properties and interactions to better understand its potential applications and develop new therapeutic approaches.
Used in Environmental and Health Safety:
1-Benzyl-3-methoxy-piperidin-4-one is used in the development of safety protocols and guidelines for its proper handling and storage. This ensures that the potential risks to human health and the environment are minimized, promoting responsible use of the compound in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 134473-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,4,7 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 134473-73:
(8*1)+(7*3)+(6*4)+(5*4)+(4*7)+(3*3)+(2*7)+(1*3)=127
127 % 10 = 7
So 134473-73-7 is a valid CAS Registry Number.

134473-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxy-1-(phenylmethyl)-4-piperidinone

1.2 Other means of identification

Product number -
Other names 1-phenylmethyl-3-methoxy-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:134473-73-7 SDS

134473-73-7Relevant academic research and scientific papers

PYRIMIDINONE DERIVATIVES AND METHODS OF USE THEREOF

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Page/Page column 163-164, (2008/12/08)

The present invention relates to Pyrimidinone Derivatives, compositions comprising a Pyrimidinone Derivative, and methods of using the Pyrimidinone Derivatives for treating or preventing obesity, diabetes, a metabolic disease, a cardiovascular disease or a disorder related to the activity of GPR119 in a patient.

STEREOISOMERIC COMPOUNDS AND METHODS FOR THE TREATMENT OF GASTROINTESTINAL AND CENTRAL NERVOUS SYSTEM DISORDERS

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Page/Page column 37-38, (2010/02/13)

The subject invention provides stereoisomeric compounds of formula (X): wherein the variables are as defined herein, and compositions for the safe and effective treatment of various gastrointestinal disorders including, but not limited to, gastroparesis,

N-aryl-N-(1-substituted-3-alkoxy-4-piperidinyl)amides and pharmaceutical compositions and methods employing such compounds

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, (2008/06/13)

This invention pertains to novel N-aryl-N-[N-substituted 3-alkoxy-4-piperidinyl]amides useful as analgesics, and methods of administering analgesia, which comprises the systemic administration to mammals of such compounds, and pharmaceutical compositions containing such compounds, wherein the novel compounds have the general formula: STR1 including optically active isomeric forms, cis/trans isomeric forms and the pharmaceutically acceptable acid addition salts therof, wherein: R is an aryl group selected from the group consisting of phenyl and substituted phenyl, wherein the substituents on the phenyl group are independently selected from the group consisting of halogen, lower-alkyl, lower-alkoxy, and combinations thereof; R1 is an alkyl group selected from the group consisting of lower-alkyl, lower-alkenyl, and lower-alkoxy lower-alkyl, each alkyl group having from 1 to 6 carbon atoms; R2 is a member selected from the group consisting of phenyl lower-alkyl, thienyl lower-alkyl, pyrazolyl lower-alkyl, tetrazolyl lower-alkyl, 4,5-dihydro-5-oxo-1H-tetrazolyl lower-alkyl, 1,3-dihydro-1,3-dioxo-2H-isoindolyl lower-alkyl, and 2,3-dihydro-2-oxo-1H-benzimidazolyl lower-alkyl; and R3 is a member selected from the group consisting of hydrogen, lower-alkyl and lower-alkyl aryl.

Novel N-(3-hydroxy-4-piperidinyl)benzamide derivatives

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, (2008/06/13)

Novel N-(3-hydroxy-4-piperidinyl)benzamides and derivatives thereof, said compounds being useful as stimulators of the motility of the gastro-intestinal system.

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