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Isolysergine is a naturally occurring alkaloid found in various plants, particularly in the seeds of the African tree Erythrophleum isovaleriana. It is structurally similar to lysergic acid, which is a key component in the synthesis of the psychoactive drug LSD. Isolysergine has been studied for its potential pharmacological properties, including its effects on the central nervous system. However, it is important to note that isolysergine itself does not have the same psychoactive effects as LSD. Research on isolysergine is limited, and its potential applications and effects are not as well understood as those of its more well-known counterparts.

478-90-0

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478-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 478-90-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 478-90:
(5*4)+(4*7)+(3*8)+(2*9)+(1*0)=90
90 % 10 = 0
So 478-90-0 is a valid CAS Registry Number.

478-90-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name isolysergine

1.2 Other means of identification

Product number -
Other names (6aR,9S)-7,9-Dimethyl-4,6,6a,7,8,9-hexahydro-indolo[4,3-fg]quinoline

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:478-90-0 SDS

478-90-0Downstream Products

478-90-0Relevant 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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