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1-(2-CHLOROPROPANOYL)-2,6-DIMETHYLPIPERIDINE is a chemical compound with a molecular formula C11H20ClNO. It is a piperidine derivative featuring a chloropropanoyl group attached to the first carbon and two methyl groups attached to the second and sixth carbons of the piperidine ring. 1-(2-CHLOROPROPANOYL)-2,6-DIMETHYLPIPERIDINE is often utilized in the synthesis of pharmaceuticals and agrochemicals, and it may hold potential applications in medicinal chemistry. Its specific properties and uses can vary based on the particular application and the chemical reactions it undergoes.

54152-06-6

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54152-06-6 Usage

Uses

Used in Pharmaceutical Synthesis:
1-(2-CHLOROPROPANOYL)-2,6-DIMETHYLPIPERIDINE is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique structure allows it to serve as a building block for creating a range of medicinal compounds, contributing to the development of new treatments and therapies.
Used in Agrochemical Synthesis:
In the agrochemical industry, 1-(2-CHLOROPROPANOYL)-2,6-DIMETHYLPIPERIDINE is used as a key component in the development of pesticides and other agricultural chemicals. Its incorporation into these products can enhance their effectiveness in protecting crops and improving overall agricultural yield.
Used in Medicinal Chemistry Research:
1-(2-CHLOROPROPANOYL)-2,6-DIMETHYLPIPERIDINE is also utilized as a research compound in the field of medicinal chemistry. Scientists and researchers use 1-(2-CHLOROPROPANOYL)-2,6-DIMETHYLPIPERIDINE to study its interactions with biological systems and to explore its potential in the development of new pharmaceutical agents.
Used as a Building Block for Organic Synthesis:
Beyond its applications in pharmaceuticals and agrochemicals, 1-(2-CHLOROPROPANOYL)-2,6-DIMETHYLPIPERIDINE can also be used as a building block for the synthesis of other organic compounds. Its versatile structure makes it a valuable component in the creation of a wide array of chemical products, from specialty chemicals to advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 54152-06-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,5 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54152-06:
(7*5)+(6*4)+(5*1)+(4*5)+(3*2)+(2*0)+(1*6)=96
96 % 10 = 6
So 54152-06-6 is a valid CAS Registry Number.

54152-06-6SDS

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-Chloro-1-(2,6-dimethyl-piperidin-1-yl)-propan-1-one

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:54152-06-6 SDS

54152-06-6Upstream product

54152-06-6Downstream Products

54152-06-6Relevant academic research and scientific papers

2 Acylaminopyridine derivatives having agonistic and antagonistic activity to morphine

Hiltmann,Hoffmeister,Niemers,Schlichting,Wollweber

, p. 584 - 600 (2007/10/04)

A search for potent analgesic substances with low abuse potentials yielded N (1 methyl 2 piperidinoethyl) N (2 pyridyl)propionamide fumarate (propiram fumarate). This compound has no chemical relationship to morphine and has morphine antagonistic as well as morphine agonistic properties. Of the derivatives of propiram tested for their analgesic efficacy, the compounds having a high analgesic potency, with a favorable therapeutic index were those in which the piperidine ring had been replaced by an azabicyclic group, the larger ring of which was a 6 or 7 membered ring. Regarding activity and toxicity, the morphine antagonistic and morphine agonistic effects of particularly interesting substances were investigated. Slight to moderate morphine antagonism was established in a number of propiram derivatives. Like propiram, these substances also have morphine agonistic properties and thus are considered partial agonists. Compounds of nalorphine type, i.e. mainly potent morphine antagonists, have not been found. A few moderately to highly effective propiram derivatives, e.g. phenyl substituted derivatives or derivatives containing an azabicyclic group, showed distinct morphine agonistic properties. These properties were in some cases very pronounced with weak or no morphine antagonism.

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