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6327-54-4

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6327-54-4 Usage

Chemical class

Phenylmethanones

Type of compound

Synthetic

Psychoactive effects

Potent hallucinogenic

Usage

Recreational drug, substitute for MDMA or ecstasy

Mechanism of action

Stimulates the release of serotonin, acts as a selective serotonin receptor agonist

Effects on mood, perception, and consciousness

Altered

Common forms

Found in party pills or combined with other substances

Adverse effects

Anxiety, nausea, increased heart rate

Legal status

Controlled substance in many countries

Potential for abuse

High due to psychoactive properties

Check Digit Verification of cas no

The CAS Registry Mumber 6327-54-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6327-54:
(6*6)+(5*3)+(4*2)+(3*7)+(2*5)+(1*4)=94
94 % 10 = 4
So 6327-54-4 is a valid CAS Registry Number.

6327-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-benzodioxol-5-yl-(3,4,5-trimethoxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names 3,4,5-trimethoxy-3',4'-methylenedioxybenzophenone

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:6327-54-4 SDS

6327-54-4Relevant articles and documents

Synthesis of phenstatin and prodrugs thereof

-

Page/Page column 9; 10, (2008/06/13)

A newly discovered antineoplastic compound denominated “phenstatin” is herein described as are synthetic methods for producing phenstatin and the active prodrug thereof. Phenstatin was converted to the sodium phosphate prodrug (3d) by a dibenzylphosphite

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