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4366-55-6

4366-55-6

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4366-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4366-55-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4366-55:
(6*4)+(5*3)+(4*6)+(3*6)+(2*5)+(1*5)=96
96 % 10 = 6
So 4366-55-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H23N3/c1-2-6-18(7-3-1)23-14-12-22(13-15-23)11-10-17-16-21-20-9-5-4-8-19(17)20/h1-9,16,21H,10-15H2

4366-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole

1.2 Other means of identification

Product number -
Other names 3-(2-(4-Phenyl-1-piperazinyl)ethyl)-1H-indole

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:4366-55-6 SDS

4366-55-6Downstream Products

4366-55-6Relevant 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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