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56361-85-4

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56361-85-4 Usage

Explanation

This is the scientific name of the compound, also known as BZP.

Explanation

BZP is a man-made substance created through chemical synthesis.

Explanation

BZP acts as both a stimulant, increasing energy and alertness, and an entactogen, inducing feelings of emotional closeness and empathy.

Explanation

BZP's chemical structure is similar to that of amphetamines, which are a class of stimulant drugs.

Explanation

BZP was initially developed and studied for its potential use in treating depression.

Explanation

Due to its stimulating and euphoria-inducing effects, BZP is now primarily used for recreational purposes.

Explanation

BZP has a similar chemical structure to MDMA and produces similar effects when consumed.

Explanation

BZP is considered to be less potent than MDMA, meaning that it has a lower capacity to produce the same effects.

Explanation

The effects of BZP typically last for a shorter period compared to MDMA.

Explanation

BZP is classified as a controlled substance in many countries due to its potential for abuse and dependence.

Explanation

BZP can produce both stimulant effects (e.g., increased energy and alertness) and hallucinogenic effects (e.g., altered perception).

Explanation

Consumption of BZP has been associated with various negative side effects, including increased heart rate, high blood pressure, and hallucinations.

Classification

Synthetic chemical compound

Functionality

Stimulant and entactogen

Structural relation

Amphetamine

Original purpose

Potential antidepressant

Current use

Recreational drug

Comparison

MDMA (ecstasy)

Potency

Less potent than MDMA

Duration of action

Shorter than MDMA

Legal status

Illegal in many countries, controlled substance

Effects

Stimulant and hallucinogenic

Adverse effects

Increased heart rate, high blood pressure, hallucinations

Check Digit Verification of cas no

The CAS Registry Mumber 56361-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,6 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 56361-85:
(7*5)+(6*6)+(5*3)+(4*6)+(3*1)+(2*8)+(1*5)=134
134 % 10 = 4
So 56361-85-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H20N2O/c23-20(16-6-2-1-3-7-16)22-12-10-15(11-13-22)18-14-21-19-9-5-4-8-17(18)19/h1-9,14-15,21H,10-13H2

56361-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(1H-indol-3-yl)piperidin-1-yl]-phenylmethanone

1.2 Other means of identification

Product number -
Other names 1-Benzoyl-4-(1H-indol-3-yl)piperidine

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:56361-85-4 SDS

56361-85-4Downstream Products

56361-85-4Relevant articles and documents

Exploring the 3-piperidin-4-yl-1H-indole scaffold as a novel antimalarial chemotype

Santos, Sofia A.,Lukens, Amanda K.,Coelho, Lis,Nogueira, Fátima,Wirth, Dyann F.,Mazitschek, Ralph,Moreira, Rui,Paulo, Alexandra

, p. 320 - 333 (2015/09/01)

A series of 3-piperidin-4-yl-1H-indoles with building block diversity was synthesized based on a hit derived from an HTS whole-cell screen against Plasmodium falciparum. Thirty-eight compounds were obtained following a three-step synthetic approach and evaluated for anti-parasitic activity. The SAR shows that 3-piperidin-4-yl-1H-indole is intolerant to most N-piperidinyl modifications. Nevertheless, we were able to identify a new compound (10d) with lead-like properties (MW = 305; cLogP = 2.42), showing antimalarial activity against drug-resistant and sensitive strains (EC50 values ~ 3 μM), selectivity for malaria parasite and no cross-resistance with chloroquine, thus representing a potential new chemotype for further optimization towards novel and affordable antimalarial drugs.

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