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N,N-diethyl-1-methylpiperidine-3-carboxamide is a chemical compound with the molecular formula C12H24N2O. It is a white crystalline solid that is soluble in organic solvents. N,N-diethyl-1-methylpiperidine-3-carboxamide is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and drugs. Its structure features a piperidine ring with a carboxamide group at the 3-position, a methyl group at the 1-position, and two ethyl groups attached to the nitrogen atoms. Due to its potential applications in the creation of active ingredients, it is an important compound in the field of medicinal chemistry.

3355-39-3

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3355-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3355-39-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,5 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3355-39:
(6*3)+(5*3)+(4*5)+(3*5)+(2*3)+(1*9)=83
83 % 10 = 3
So 3355-39-3 is a valid CAS Registry Number.

3355-39-3SDS

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 N,N-diethyl-1-methylpiperidine-3-carboxamide

1.2 Other means of identification

Product number -
Other names N,N-diethyl-1-methylnipecotamide

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:3355-39-3 SDS

3355-39-3Downstream Products

3355-39-3Relevant academic research and scientific papers

Substituted piperidines

-

, (2008/06/13)

The compounds are of the heterocyclic class of 2-phenethylpiperidines having an amido substituent in the ortho position of the phenethyl moiety. Substituents in the ortho position include formamido, benzamido, cinnamamido, 2-thiophenecarboxamido, alkanesulfonamido and alkanoylamido. They are useful as antiarrhythmic and/or antiserotonin agents. The novel compounds are prepared by reaction of appropriately substituted o-aminophenethylpiperidines and the carbonyl or sulfonyl halides or anhydrides. Typical embodiments of this invention are 4-methoxy-2'-[2-(1-methyl-2-piperidyl)ethyl]benzanilide and 2'-[2-(1-methyl-2-piperidyl)ethyl]cinnamanilide.

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