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77509-75-2

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77509-75-2 Usage

Description

1-(1-Benzofuran-2-ylcarbonyl)piperidine, a chemical compound with the molecular formula C16H17NO2, is a piperidine derivative featuring a benzofuran-2-ylcarbonyl group attached to the piperidine ring. 1-(1-BENZOFURAN-2-YLCARBONYL)PIPERIDINE is frequently utilized in pharmaceutical research and drug development due to its potential biological activities.

Uses

Used in Pharmaceutical Research and Drug Development:
1-(1-Benzofuran-2-ylcarbonyl)piperidine is used as a compound with potential biological activities for the development of new medications. Its properties make it a promising candidate for various therapeutic applications.
Used in Treatment of Mood Disorders:
In the field of psychiatry, 1-(1-Benzofuran-2-ylcarbonyl)piperidine is used as a potential serotonin reuptake inhibitor for the treatment of depression and other mood disorders. Its ability to modulate serotonin levels could provide relief for patients suffering from these conditions.
Used in Pain Management:
1-(1-Benzofuran-2-ylcarbonyl)piperidine is also being investigated for its potential anti-inflammatory and analgesic properties. It may be used as a component in the development of new medications for pain management, offering an alternative to existing treatments and potentially improving patient outcomes.
Used in the Development of Serotonin Reuptake Inhibitors:
Within the pharmaceutical industry, 1-(1-Benzofuran-2-ylcarbonyl)piperidine is used as a key compound in the development of serotonin reuptake inhibitors. Its structure and properties make it a valuable asset in creating new drugs to treat mood disorders effectively.
Used in the Creation of Anti-Inflammatory and Analgesic Medications:
In the field of medicinal chemistry, 1-(1-Benzofuran-2-ylcarbonyl)piperidine is used as a building block for the creation of anti-inflammatory and analgesic medications. Its potential properties in these areas could lead to the development of novel drugs with improved efficacy and reduced side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 77509-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,0 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77509-75:
(7*7)+(6*7)+(5*5)+(4*0)+(3*9)+(2*7)+(1*5)=162
162 % 10 = 2
So 77509-75-2 is a valid CAS Registry Number.

77509-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzofuran-2-yl(piperidin-1-yl)methanone

1.2 Other means of identification

Product number -
Other names benzofuran-2-carboxylic acid piperidide

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:77509-75-2 SDS

77509-75-2Relevant articles and documents

Hydrosilane-Mediated Electrochemical Reduction of Amides

Okamoto, Kazuhiro,Nagahara, Shingo,Imada, Yasushi,Narita, Risako,Kitano, Yoshikazu,Chiba, Kazuhiro

, p. 15992 - 16000 (2021/07/20)

Electrochemical reduction of amides was achieved by using a hydrosilane without any toxic or expensive metals. The key reactive ketyl radical intermediate was generated by cathodic reduction. Continuous reaction with anodically generated silyl radicals or zinc bromide resulted in chemoselective deoxygenation to give the corresponding amines.

Synthesis of 4-(2-Benzofuranyl)coumarins

Deshpande, A. R.,Joshi, U. K.,Paradkar, M. V.

, p. 524 - 526 (2007/10/02)

4-(2-Benzofuranyl)coumarins (3) have been synthesized by two routes, one involving Pechmann condensation of benzofuranpropionic acid-β-oxo-ethyl ester with phenols and the other involving Wittig reaction on 2-(2-hydroxybenzoyl)benzofuran using Ph3P=CHCOOE

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