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(2-bromo-4,5-dimethoxyphenyl)(3,4-dihydroquinolin-1(2H)-yl)methanone, also known as BDMP-DHQ, is a chemical compound with potential psychoactive properties. It belongs to the class of designer drugs called synthetic cannabinoids, which can mimic the effects of natural cannabis. BDMP-DHQ is a cannabinoid receptor agonist, which means it binds to and activates the same receptors in the brain as THC, the active ingredient in marijuana. This can lead to changes in mood, perception, and cognition, and may cause psychoactive effects.

65367-73-9

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65367-73-9 Usage

Uses

Used in Psychoactive Applications:
BDMP-DHQ is used as a psychoactive substance for its ability to mimic the effects of natural cannabis. As a cannabinoid receptor agonist, it binds to and activates the same receptors in the brain as THC, leading to changes in mood, perception, and cognition. However, there is limited research on the specific effects and potential health risks of BDMP-DHQ, so caution and medical advice should be sought before using any psychoactive substances.

Check Digit Verification of cas no

The CAS Registry Mumber 65367-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,6 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65367-73:
(7*6)+(6*5)+(5*3)+(4*6)+(3*7)+(2*7)+(1*3)=149
149 % 10 = 9
So 65367-73-9 is a valid CAS Registry Number.

65367-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-bromo-4,5-dimethoxyphenyl)-(3,4-dihydro-2H-quinolin-1-yl)methanone

1.2 Other means of identification

Product number -
Other names 6-bromo-3,4-dimethoxy-N-tetrahydroquinolyl-benzamide

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:65367-73-9 SDS

65367-73-9Downstream Products

65367-73-9Relevant academic research and scientific papers

Intramolecular direct dehydrohalide coupling promoted by KOtBu: Total synthesis of amaryllidaceae alkaloids anhydrolycorinone and oxoassoanine

De, Subhadip,Ghosh, Santanu,Bhunia, Subhajit,Sheikh, Javeed Ahmad,Bisai, Alakesh

supporting information, p. 4466 - 4469 (2012/10/29)

A transition-metal-free intramolecular dehydrohalide coupling via intramolecular homolytic aromatic substitution (HAS) with aryl radicals has been developed in the presence of potassium tert-butoxide and an organic molecule as the catalyst. The methodology has been applied to a concise synthesis of Amaryllidaceae alkaloids viz. oxoassoanine (1b), anhydrolycorinone (1d), and other related structures. Interestingly, the method also works only in the presence of potassium tert-butoxide.

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