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1-Piperidinecarboxamide, 2-methyl-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27098-56-2

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27098-56-2 Usage

Molecular Weight

204.27 g/mol

Structure

A piperidine ring with a carboxamide group at position 1 and a methyl group at position 2, and a phenyl ring attached to the nitrogen atom.

Physical Properties

It is a solid with a melting point of 92-94°C.

Reactivity

It can react with various reagents to form different derivatives and analogs.

Uses

It is used as a precursor in the synthesis of pharmaceuticals and organic compounds, and has been studied for its potential use as a medication for treating pain and neurodegenerative diseases.

Importance

It is an important chemical in the field of pharmaceuticals and research due to its application as a building block in the creation of different drugs and organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 27098-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,9 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 27098-56:
(7*2)+(6*7)+(5*0)+(4*9)+(3*8)+(2*5)+(1*6)=132
132 % 10 = 2
So 27098-56-2 is a valid CAS Registry Number.

27098-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-N-phenylpiperidine-1-carboxamide

1.2 Other means of identification

Product number -
Other names 2-Methyl-piperidin-1-carbonsaeure-anilid

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:27098-56-2 SDS

27098-56-2Relevant academic research and scientific papers

Synthesis of unsymmetrical phenylurea derivatives via oxidative cross coupling of aryl formamides with amines under metal-free conditions

Reddy, Nagireddy Veera,Kumar, Pailla Santhosh,Reddy, Peddi Sudhir,Kantam, Mannepalli Lakshmi,Reddy, Kallu Rajender

supporting information, p. 805 - 809 (2015/02/19)

A new synthetic approach for phenylurea derivatives involving the cross coupling of N-aryl formamides with amines through the formation of isocyanate intermediates in the presence of hypervalent iodine reagents is described.

Acetoacetanilides as masked isocyanates: Facile and efficient synthesis of unsymmetrically substituted ureas

Wei, Ying,Liu, Jing,Lin, Shaoxia,Ding, Hongqian,Liang, Fushun,Zhao, Baozhong

supporting information; experimental part, p. 4220 - 4223 (2010/11/04)

Figure Presented. A general and practical method for the preparation of unsymmetrically substituted ureas has been developed. By the reactions of acetoacetanilides with various amines including primary/secondary amines, a series of substituted aryl ureas were achieved in high yields. Acetoacetanilide substrates can be considered as masked reagents that liberate reactive isocyanates in situ.

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