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54261-07-3

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54261-07-3 Usage

Description

1-(2-bromobutanoyl)piperidine is a chemical compound characterized by the molecular formula C10H17BrNO. It is a derivative of piperidine, a heterocyclic amine, featuring a butanoyl group and a bromine atom attached to its structure. 1-(2-bromobutanoyl)piperidine is known for its reactivity due to the presence of the bromine atom, which allows it to participate in various chemical reactions. As a result, 1-(2-bromobutanoyl)piperidine is a valuable component in the chemical industry and holds potential for use in medicinal chemistry for drug development and research purposes.

Uses

Used in Pharmaceutical Industry:
1-(2-bromobutanoyl)piperidine is used as a building block in organic synthesis for the development of pharmaceuticals. Its unique structure and reactivity make it a promising candidate for creating new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(2-bromobutanoyl)piperidine is utilized as a component in the synthesis of various agrochemicals. Its chemical properties contribute to the development of effective products for agricultural applications.
Used in Specialty Chemicals Production:
1-(2-bromobutanoyl)piperidine is also employed in the production of specialty chemicals, where its distinctive structure and reactivity are harnessed to create compounds with specific applications in various industries.
Used in Medicinal Chemistry Research:
Due to its potential pharmacological properties, 1-(2-bromobutanoyl)piperidine is used in medicinal chemistry for drug development and research. Its unique structure allows for the exploration of new therapeutic avenues and the creation of novel compounds with targeted effects.

Check Digit Verification of cas no

The CAS Registry Mumber 54261-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,6 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54261-07:
(7*5)+(6*4)+(5*2)+(4*6)+(3*1)+(2*0)+(1*7)=103
103 % 10 = 3
So 54261-07-3 is a valid CAS Registry Number.

54261-07-3SDS

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 1-(2-Bromobutanoyl)piperidine

1.2 Other means of identification

Product number -
Other names N-(2-Brom-n-butyryl)-piperidin

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:54261-07-3 SDS

54261-07-3Downstream Products

54261-07-3Relevant articles and documents

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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