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[2-(4-Methoxy-phenyl)-ethyl]-methyl-amine hydrochloride, also known as 4-Methoxyphenyl-ethyl-methyl-amine hydrochloride, is a chemical compound belonging to the phenethylamine class of drugs. It is a derivative of amphetamine with the molecular formula C11H17NO. This psychoactive substance is typically found in the form of a white crystalline powder and is soluble in water. Due to its potential for abuse, it is classified as a controlled substance in many countries and has been reported to exhibit sympathomimetic and hallucinogenic effects.

35803-88-4

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35803-88-4 Usage

Uses

Used in Pharmaceutical Synthesis:
[2-(4-METHOXY-PHENYL)-ETHYL]-METHYL-AMINE HYDROCHLORIDE is used as an intermediate in the synthesis of other pharmaceuticals and research chemicals. It serves as a key component in the production of various medications, contributing to their therapeutic effects.
Used in Research:
In the scientific community, [2-(4-METHOXY-PHENYL)-ETHYL]-METHYL-AMINE HYDROCHLORIDE is used as a research chemical for studying its psychoactive properties and potential applications in medicine. Researchers utilize [2-(4-METHOXY-PHENYL)-ETHYL]-METHYL-AMINE HYDROCHLORIDE to explore its effects on the central nervous system and its interactions with various receptors, aiming to develop a better understanding of its mechanisms of action and potential therapeutic uses.
Used in Controlled Substances Regulation:
Due to its psychoactive properties and potential for abuse, [2-(4-METHOXY-PHENYL)-ETHYL]-METHYL-AMINE HYDROCHLORIDE is used in the development and enforcement of controlled substances regulations. Governments and regulatory agencies classify and monitor [2-(4-METHOXY-PHENYL)-ETHYL]-METHYL-AMINE HYDROCHLORIDE to prevent its misuse and ensure that it is used safely and appropriately in medical and research settings.

Check Digit Verification of cas no

The CAS Registry Mumber 35803-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,0 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 35803-88:
(7*3)+(6*5)+(5*8)+(4*0)+(3*3)+(2*8)+(1*8)=124
124 % 10 = 4
So 35803-88-4 is a valid CAS Registry Number.

35803-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(4-METHOXY-PHENYL)-ETHYL]-METHYL-AMINE HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names (4-Methoxy-phenaethyl)-methyl-amin,Hydrochlorid

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:35803-88-4 SDS

35803-88-4Downstream Products

35803-88-4Relevant academic research and scientific papers

THERAPEUTIC AGENT FOR CEREBRAL INFARCTION

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, (2012/08/08)

The invention provides a therapeutic drug for ischemic stroke. The therapeutic drug has the formula (I) wherein each symbol is as defined herein, or a pharmacologically acceptable salt thereof, or a solvate thereof, as an active ingredient.

PROCESS FOR PREPARING N-METHYL-3, 4-DIMETHOXYPHENYLETHYLAMINE

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Page/Page column 7, (2009/07/17)

Provided are intermediates useful for the preparation of verapamil and methods for their preparation.

Compound 48/80. Structure activity relations and poly THIQ, a new, more potent analog

Read,Kiefer,Weber

, p. 1292 - 1295 (2007/10/04)

Derivatives of p methoxyphenethylmethylamine were synthesized from which formaldehyde copolymers analogous to compound 48/80 were prepared. Measurement of the hypotensive activity of these analogs revealed that potency was not enhanced by changing the group in the para position, by varying the length of the alkyl group, or by altering the degree of methylation of the amine. However, when the ethylamine side chain was cyclized to form 7 methoxytetrahydroisoquinoline, the copolymer prepared from this derivative (poly THIQ) was seven times more potent than compound 48/80. The hypotensive action of poly THIQ was found to result from the liberation of histamine, as with compound 48/80.

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