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1935-33-7

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1935-33-7 Usage

Chemical class

Ergoline derivative

Structural similarity

Lysergic acid diethylamide (LSD)

Psychoactive properties

Yes

Effects on the central nervous system

Yes

Affinity for serotonin receptors

Yes

Hallucinogenic properties

Potentially present

Dopaminergic effects

Yes

Adrenergic effects

Yes

Stimulating effects

Potentially present

Euphoric effects

Potentially present

Recreational use

Potential interest

Therapeutic use

Potential interest

Ongoing research

Yes

Legal status

Varies by country, may be controlled or restricted

Safety and side effects

Not well-established, use with caution
Please note that the information provided is based on the given material and may not be exhaustive. It is essential to consult scientific literature and professional sources for a more comprehensive understanding of 1,6,8-trimethyl-8,9-didehydroergoline.

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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