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3-(4-METHOXYPHENYL)PROPYLAMINE HCL, also known as 4-Methoxyamphetamine HCl, is a synthetic chemical compound belonging to the class of organic compounds known as amphetamines and derivatives. It is an organic compound containing or derived from 1-phenylpropan-2-amine and is typically found in a highly stable hydrochloride form (HCL), which enhances its storage and handling. 3-(4-METHOXYPHENYL)PROPYLAMINE HCL is primarily used for research and development purposes in the field of neuropharmacology. However, due to its psychoactive properties, the amateur use or misuse of 3-(4-METHOXYPHENYL)PROPYLAMINE HCL can lead to severe health implications, and it is regulated as a controlled substance in many countries.

36397-51-0

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36397-51-0 Usage

Uses

Used in Neuropharmacological Research:
3-(4-METHOXYPHENYL)PROPYLAMINE HCL is used as a research chemical for studying the effects of amphetamines and their derivatives on the central nervous system. It aids in understanding the mechanisms of action, potential therapeutic applications, and the risks associated with the misuse of psychoactive substances.
Used in Controlled Substances Regulation:
3-(4-METHOXYPHENYL)PROPYLAMINE HCL is used as a controlled substance in many countries to prevent its misuse and amateur use, which can lead to severe health implications. The regulation ensures that the compound is only used for legitimate research and development purposes in a controlled and safe environment.
Used in Drug Development:
3-(4-METHOXYPHENYL)PROPYLAMINE HCL is used as a starting material or intermediate in the development of new drugs with potential therapeutic applications. Its unique chemical structure and properties make it a valuable compound for the synthesis of novel pharmaceuticals targeting various neurological disorders and conditions.
Used in Toxicological Studies:
3-(4-METHOXYPHENYL)PROPYLAMINE HCL is used as a test compound in toxicological studies to evaluate the potential adverse effects of amphetamines and their derivatives on human health. These studies help in understanding the risks associated with the misuse of psychoactive substances and contribute to the development of safer and more effective treatments.
Used in Forensic Analysis:
3-(4-METHOXYPHENYL)PROPYLAMINE HCL is used as a reference compound in forensic analysis to identify and quantify the presence of amphetamines and their derivatives in biological samples. This helps in the investigation of drug-related crimes and the assessment of drug abuse patterns in the population.

Check Digit Verification of cas no

The CAS Registry Mumber 36397-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,9 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 36397-51:
(7*3)+(6*6)+(5*3)+(4*9)+(3*7)+(2*5)+(1*1)=140
140 % 10 = 0
So 36397-51-0 is a valid CAS Registry Number.

36397-51-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methoxyphenyl)propan-1-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names 3-(4-methoxyphenyl)propan-1-amine hydrochloride

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:36397-51-0 SDS

36397-51-0Relevant articles and documents

Direct Primary Amination of Alkylmetals with NH-Oxaziridine

Behnke, Nicole Erin,Kielawa, Russell,Kwon, Doo-Hyun,Ess, Daniel H.,Kürti, László

supporting information, p. 8064 - 8068 (2019/01/04)

A method for the primary electrophilic amination of primary, secondary, and tertiary organometallic substrates from a bench-stable NH-oxaziridine reagent is described. This facile and highly chemoselective transformation occurs at ambient temperature and without transition metal catalysts or purification by column chromatography to provide alkylamine products in a single step. Density functional theory (DFT) calculations revealed that, despite the basicity of alkylmetals, the direct NH-transfer pathway is favored over proton and O-transfer.

Borrowing hydrogen methodology for the conversion of alcohols into N-protected primary amines and in situ deprotection

Lamb, Gareth W.,Watson, Andrew J.A.,Jolley, Katherine E.,Maxwell, Aoife C.,Williams, Jonathan M.J.

experimental part, p. 3374 - 3377 (2009/09/05)

Alcohols have been converted into a range of protected amines including sulfonamides and N-alkylbenzylamine derivatives. Representative examples of deprotection to afford primary amines are also provided.

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