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203186-44-1

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203186-44-1 Usage

General Description

1-(2-methylbenzoyl)piperidin-4-one is a chemical compound with the molecular formula C15H17NO2. It belongs to the class of piperidinones and is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. 1-(2-methylbenzoyl)piperidin-4-one is a yellow-orange solid at room temperature and has a melting point of 94-96°C. It is known for its potential as a drug targeting the central nervous system, and is also being studied for its potential as an anti-inflammatory and analgesic agent. Additionally, 1-(2-methylbenzoyl)piperidin-4-one is a versatile intermediate in organic synthesis and is frequently utilized in the production of other complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 203186-44-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,1,8 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 203186-44:
(8*2)+(7*0)+(6*3)+(5*1)+(4*8)+(3*6)+(2*4)+(1*4)=101
101 % 10 = 1
So 203186-44-1 is a valid CAS Registry Number.

203186-44-1SDS

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-(2-Methylbenzoyl)-4-piperidinone

1.2 Other means of identification

Product number -
Other names 1-(2-methylbenzoyl)piperidin-4-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:203186-44-1 SDS

203186-44-1Relevant articles and documents

Synthesis and SAR of analogs of the M1 allosteric agonist TBPB. Part II: Amides, sulfonamides and ureas-The effect of capping the distal basic piperidine nitrogen

Miller, Nicole R.,Daniels, R. Nathan,Bridges, Thomas M.,Brady, Ashley E.,Conn, P. Jeffrey,Lindsley, Craig W.

scheme or table, p. 5443 - 5447 (2009/05/30)

This letter describes the further synthesis and SAR, developed through an iterative analog library approach, of analogs of the highly selective M1 allosteric agonist TBPB by deletion of the distal basic piperidine nitrogen by the formation of amides, sulf

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