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61220-24-4

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61220-24-4 Usage

Structure

Complex organic compound with a benzimidazole core structure and side chains containing an indole and piperidine moiety

Properties

Fused heterocyclic compound with potential pharmaceutical applications

Potential biological activity

Molecular structure suggests potential biological activity, making it a candidate for drug development or medicinal chemistry research

Further studies needed

Additional research is necessary to explore its potential pharmacological properties and applications

Check Digit Verification of cas no

The CAS Registry Mumber 61220-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,2 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61220-24:
(7*6)+(6*1)+(5*2)+(4*2)+(3*0)+(2*2)+(1*4)=74
74 % 10 = 4
So 61220-24-4 is a valid CAS Registry Number.

61220-24-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[1-(2-indol-3-yl-ethyl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one

1.2 Other means of identification

Product number -
Other names 1-{1-[2-(1H-Indol-3-yl)-ethyl]-piperidin-4-yl}-1,3-dihydro-benzoimidazol-2-one

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:61220-24-4 SDS

61220-24-4Downstream Products

61220-24-4Relevant articles and documents

Investigations into the mechanism of lactamization of lactones yielding in a novel route to biologically active tryptamine derivatives

Decker, Michael,Nguyen, Thi Thanh Huyen,Lehmann, Jochen

, p. 4567 - 4578 (2007/10/03)

The mechanism of lactamization of corresponding lactones was investigated by means of gas chromatography and synthesis of possible intermediates as references. Lactones react with amines via the amino acid with subsequent elimination of water to the corresponding lactams. In the first step, also hydroxyamides are in equilibrium with the lactones and amines, respectively, which are not able to form the amide though. This mechanism opens a new approach for the synthesis of Nβ-disubstituted tryptamines.

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