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39201-78-0

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39201-78-0 Usage

General Description

3,5-Dimethoxy-4-propoxybenzeneethanaminium is a chemical compound with a long name, commonly known as 3C-P. It is a psychoactive drug that belongs to the phenethylamine class and is structurally related to mescaline. 3C-P is known for its hallucinogenic effects and is often used recreationally for its mind-altering properties. It is a potent serotonin receptor agonist and can produce intense visual and auditory hallucinations, as well as alterations in perception and mood. The compound is not approved for medical use and is considered a designer drug, meaning it is synthesized to mimic the effects of illegal substances while attempting to evade regulation. Due to its potential for abuse and the risks associated with its use, 3C-P is classified as a controlled substance in many countries.

Check Digit Verification of cas no

The CAS Registry Mumber 39201-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,0 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 39201-78:
(7*3)+(6*9)+(5*2)+(4*0)+(3*1)+(2*7)+(1*8)=110
110 % 10 = 0
So 39201-78-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H21NO3/c1-4-7-17-13-11(15-2)8-10(5-6-14)9-12(13)16-3/h8-9H,4-7,14H2,1-3H3

39201-78-0SDS

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 2-(3,5-dimethoxy-4-propoxyphenyl)ethanamine

1.2 Other means of identification

Product number -
Other names 4-Propoxy-3,5-DMPEA

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:39201-78-0 SDS

39201-78-0Synthetic route

(3,5-Dimethoxy-4-propoxy-phenyl)-acetonitrile
61367-65-5

(3,5-Dimethoxy-4-propoxy-phenyl)-acetonitrile

3,5-Dimethoxy-4-n-propyloxy-β-phenoaethylamin
39201-78-0

3,5-Dimethoxy-4-n-propyloxy-β-phenoaethylamin

Conditions
ConditionsYield
With hydrogenchloride; hydrogen; palladium on activated charcoal In ethanol
4-hydroxy-3,5-dimethoxyphenylacetonitrile
42973-55-7

4-hydroxy-3,5-dimethoxyphenylacetonitrile

3,5-Dimethoxy-4-n-propyloxy-β-phenoaethylamin
39201-78-0

3,5-Dimethoxy-4-n-propyloxy-β-phenoaethylamin

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: K2CO3 / acetone
2: H2, aq. HCl / Pd-C / ethanol
View Scheme

39201-78-0Downstream Products

39201-78-0Relevant articles and documents

Lipophilicity and serotonin agonist activity in a series of 4 substituted mescaline analogues

Nichols,Dyer

, p. 299 - 301 (2007/10/06)

Replacement of the 4 methoxy of mescaline with higher alkyl homologues or with bromine led to increased activity at serotonin receptors in a sheep umbilical artery preparation. This activity appears correlated with lipophilicity, as measured by 1 octanol water partition coefficients, but drops off when the 4 substituent is about five atoms in length. It is suggested that 3,4,5 trisubstitution may give compounds which are as active as those with the 2,4 5 substitution pattern.

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