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(8beta)-6,8-Dimethyl-9,10-didehydroergoline is a chemical compound belonging to the ergoline family, which is a group of alkaloids derived from the ergot fungus. This specific compound is characterized by its unique structure, featuring a 6,8-dimethyl substitution and a 9,10-didehydro functional group. It is known for its potential applications in pharmaceutical research, particularly in the development of drugs targeting the central nervous system. The compound's structure and properties make it a subject of interest for scientists exploring its potential therapeutic effects and mechanisms of action.

519-10-8

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519-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 519-10-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 519-10:
(5*5)+(4*1)+(3*9)+(2*1)+(1*0)=58
58 % 10 = 8
So 519-10-8 is a valid CAS Registry Number.

519-10-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (9R)-7,9-dimethyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline

1.2 Other means of identification

Product number -
Other names Lysergine

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:519-10-8 SDS

519-10-8Downstream Products

519-10-8Relevant academic research and scientific papers

TOTAL SYNTHESIS OF ERGOT ALKALOID (+/-)-FUMIGACLAVINE B

Kiguchi, Toshiko,Hashimoto, Chiyomi,Ninomiya, Ichiya

, p. 1925 - 1928 (2007/10/02)

The synthetic route developed on the despyrrole analogs of clavines was succesfully applied to the first total synthesis of (+/-)-fumigaclavine B (1) and (+/-)-isolysergine (2), thus firmly established the structure of the former alkaloid (1).

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