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5-methyl-5-phenylpiperidin-2-one, also known as 5-Methyl-5-phenyl-2-piperidinone, is a chemical compound with the molecular formula C13H17NO. It is a white powder with a molecular weight of 203.28 g/mol. 5-methyl-5-phenylpiperidin-2-one is commonly used in the synthesis of pharmaceuticals and other organic compounds. It has been studied for its potential pharmacological properties, including its activity as an analgesic and antipsychotic. The substance is considered to be relatively stable and compatible with many other chemicals, making it useful for various chemical processes in research and industry. However, it should be handled with care due to its potential irritant and harmful effects if ingested, inhaled, or in contact with the skin or eyes.

7149-39-5

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7149-39-5 Usage

Uses

Used in Pharmaceutical Industry:
5-methyl-5-phenylpiperidin-2-one is used as an intermediate in the synthesis of pharmaceuticals for its potential pharmacological properties. It is utilized in the development of drugs that target pain relief and mental health disorders, specifically as an analgesic and antipsychotic agent.
Used in Organic Chemistry Research:
5-methyl-5-phenylpiperidin-2-one is used as a reagent and building block in organic chemistry for the synthesis of various organic compounds. Its stability and compatibility with other chemicals make it a valuable component in chemical processes, facilitating the creation of new molecules and materials for research purposes.
Used in Chemical Process Development:
Due to its compatibility with a wide range of chemicals, 5-methyl-5-phenylpiperidin-2-one is used in the development of chemical processes in the research and industrial sectors. It aids in the optimization of reactions and the production of desired compounds with improved efficiency and yield.
Safety Considerations:
While 5-methyl-5-phenylpiperidin-2-one has various applications, it is important to handle it with care due to its potential irritant and harmful effects. It should be used in controlled environments and with appropriate safety measures to prevent ingestion, inhalation, or contact with the skin and eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 7149-39-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7149-39:
(6*7)+(5*1)+(4*4)+(3*9)+(2*3)+(1*9)=105
105 % 10 = 5
So 7149-39-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO/c1-12(8-7-11(14)13-9-12)10-5-3-2-4-6-10/h2-6H,7-9H2,1H3,(H,13,14)

7149-39-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-5-phenylpiperidin-2-one

1.2 Other means of identification

Product number -
Other names 5-methyl-5-phenyl-piperidin-2-one

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:7149-39-5 SDS

7149-39-5Upstream product

7149-39-5Downstream Products

7149-39-5Relevant academic research and scientific papers

Visible Light-Promoted Three-Component Carboazidation of Unactivated Alkenes with TMSN3 and Acrylonitrile

Yang, Bo,Ren, Xiang,Shen, Xuzhong,Li, Tongtong,Lu, Zhan

, p. 1017 - 1023 (2018/09/25)

A novel difunctionalization of unactivated alkenes has been reported via visible light-promoted three-component carboazidation using TMSN3 and acrylonitrile as partners without any stoichiometric oxidants. This protocol is operationally simple for straightforward access to azido derivatives with good functional group tolerance from readily available starting materials. A facile azido radical-catalyzed [3?+?2] cycloaddition reaction of vinylcyclopropane with acrylonitrile was also observed to deliver a multi-substituted cyclopentane.

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