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30256-73-6

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30256-73-6 Usage

General Description

1-(1H-indol-3-yl)-2-(piperidin-1-yl)ethanone is a chemical compound that consists of an indole group and a piperidine group connected by an ethanone linker. It is known for its potential pharmacological activity, particularly as a potential drug candidate for various therapeutic applications. The compound has been studied for its potential anti-inflammatory, anticonvulsant, and antitumor properties, and it has shown promise in preclinical studies. Its unique structure and potential biological activities make it an interesting target for further research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 30256-73-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,2,5 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30256-73:
(7*3)+(6*0)+(5*2)+(4*5)+(3*6)+(2*7)+(1*3)=86
86 % 10 = 6
So 30256-73-6 is a valid CAS Registry Number.

30256-73-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1H-indol-3-yl)-2-piperidin-1-ylethanone

1.2 Other means of identification

Product number -
Other names indol-3-yl piperidinomethyl ketone

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:30256-73-6 SDS

30256-73-6Downstream Products

30256-73-6Relevant articles and documents

QUINOLIZIDINES. IX. AN IMPROVED PROCEDURE FOR THE SYNTHESIS OF INDOLOQUINOLIZIDINE FROM 3-(2-PIPERIDINOETHYL)INDOLE

Fujii, Tozo,Ohba, Masashi,Sasaki, Noriko

, p. 1805 - 1810 (2007/10/02)

The procedure and yield of the oxidative cyclization of 3-(2-piperidinoethyl)indole (V) to produce indoloquinolizidine (X) have been improved by the use of 3 molar equivalents of Hg(OAc)2-edetate disodium in boiling aqueous EtOH for 3 h.Similar oxidation of the piperidinoethanol IIIb in boiling 1percent aqueous AcOH failed to give the expected lactam alcohol XIIb, an alternative intermediate for the synthesis of X.

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