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1935-33-7

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1935-33-7 Usage

General Description

1,6,8-trimethyl-8,9-didehydroergoline is a chemical compound that belongs to the ergoline family, which is known for its psychoactive properties. It is a derivative of ergoline and is structurally similar to lysergic acid diethylamide (LSD). 1,6,8-trimethyl-8,9-didehydroergoline has been studied for its effects on the central nervous system and has been found to have affinity for a variety of serotonin receptors, which may account for its hallucinogenic and psychoactive properties. It is also known to have dopaminergic and adrenergic effects, which may contribute to its stimulating and euphoric effects. Research on 1,6,8-trimethyl-8,9-didehydroergoline is ongoing, but its potential for recreational and therapeutic use has garnered interest in the scientific community.

Check Digit Verification of cas no

The CAS Registry Mumber 1935-33-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,3 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1935-33:
(6*1)+(5*9)+(4*3)+(3*5)+(2*3)+(1*3)=87
87 % 10 = 7
So 1935-33-7 is a valid CAS Registry Number.

1935-33-7SDS

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 (6aR,10aR)-4,7,9-trimethyl-6,6a,8,10a-tetrahydroindolo[4,3-fg]quinoline

1.2 Other means of identification

Product number -
Other names methyl adamantane

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:1935-33-7 SDS

1935-33-7Downstream Products

1935-33-7Relevant articles and documents

Partial Synthesis of New Ergoline Derivatives from Clavine Alkaloids, III: O-Acyl- and O-Alkyl-1,6-dimethyl-8-(hydroxymethyl)ergol-9-enes

Eich, Eckart

, p. 781 - 788 (2007/10/02)

Elymoclavine (1), lysergole (2) and O-acyllysergoles are primarily methylated at the indole nitrogen when reacted with potassium and methyl iodide in ammonia.By variation of the reaction conditions, 1 and 2 can also by methylated at the hydroxy group.Thus, 1-methyl lysergole ethers can by prepared by the same method with different alkyl iodides.On the other hand, ester syntheses according to Williamson starting from 17-halogenoergolenes are not successful.

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