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17367-93-0

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17367-93-0 Usage

General Description

4,5-Methylenedioxyindole is a chemical compound with a molecular formula C9H7NO2 and a molar mass of 161.16 g/mol. It is a derivative of the heterocyclic compound indole, and is known for its psychoactive properties. 4,5-METHYLENEDIOXYINDOLE has been studied for its potential use in treating mental disorders and neurodegenerative diseases. It has also been investigated for its potential as a therapeutic agent in the treatment of drug addiction and withdrawal symptoms. 4,5-Methylenedioxyindole is also a precursor in the synthesis of other indole derivatives and has shown potential in the development of new drugs with various pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 17367-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,6 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17367-93:
(7*1)+(6*7)+(5*3)+(4*6)+(3*7)+(2*9)+(1*3)=130
130 % 10 = 0
So 17367-93-0 is a valid CAS Registry Number.

17367-93-0SDS

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 6H-[1,3]dioxolo[4,5-e]indole

1.2 Other means of identification

Product number -
Other names 4,5-Methylenedioxyindole

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:17367-93-0 SDS

17367-93-0Downstream Products

17367-93-0Relevant articles and documents

Structure-Activity Relationships in Potentially Hallucinogenic N,N-Dialkyltryptamines Substituted in the Benzene Moiety

Kline, Toni B.,Benington, Frederick,Morin, Richard D.,Beaton, John M.

, p. 908 - 913 (1982)

A series of N,N-dialkyltryptamines with methylthio or methylenedioxy substituents in the 4, 5, and 6 positions and methyl or isopropyl on the side-chain nitrogen has been synthesized.The behavioral pharmacology of these compounds showed them to posses Bovet-Gatti profiles characteristic of hallucinogens, and the 5-methylthio congener was the most potent.Binding studies at LSD and 5-HT sites demonstrated that no single structural feature correlated with binding or behavioral changes and suggest a complex mode of action for these potential hallucinogenic agents.

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