CAS 3937-16-4

2,3,4-Trimethoxyphenethylamine

Description:

2,3,4-Trimethoxyphenethylamine, with the CAS number 3937-16-4, is a chemical compound belonging to the class of phenethylamines. It features a phenethylamine backbone, characterized by a two-carbon ethyl chain attached to a phenolic ring, which is further substituted with three methoxy groups at the 2, 3, and 4 positions of the aromatic ring. This substitution pattern contributes to its unique chemical properties and potential biological activity. The presence of methoxy groups typically enhances the lipophilicity of the compound, potentially influencing its ability to cross biological membranes. As a phenethylamine derivative, it may exhibit psychoactive properties, although specific pharmacological effects can vary widely based on structural modifications. The compound is of interest in various fields, including medicinal chemistry and neuroscience, for its potential applications in research related to neurotransmitter systems. However, detailed studies on its safety, efficacy, and specific interactions are necessary to fully understand its characteristics and potential uses.

Formula: C₁₁H₁₇NO₃

InChI: InChI=1S/C11H17NO3/c1-13-9-5-4-8(6-7-12)10(14-2)11(9)15-3/h4-5H,6-7,12H2,1-3H3

InChI key: InChIKey=PVLFQRLVSMMSQK-UHFFFAOYSA-N

SMILES: O(C)C1=C(OC)C(OC)=CC=C1CCN

Synonyms:

• 2,3,4-Trimethoxy-β-phenethylamine
• 2,3,4-Trimethoxybenzeneethanamine
• 2,3,4-Trimethoxyphenethylamine
• 2,3,4-Trimethoxyphenylethylamine
• 2-(2,3,4-Trimethoxyphenyl)Ethan-1-Amine
• 2-(2,3,4-Trimethoxyphenyl)ethylamine
• Benzeneethanamine, 2,3,4-Trimethoxy-
• Phenethylamine, 2,3,4-trimethoxy-

2-(2,3,4-Trimethoxyphenyl)ethan-1-amine

Controlled Product

CAS: 3937-16-4

2-(2,3,4-Trimethoxyphenyl)ethan-1-amine is a drug with anti-diabetic properties that belongs to the class of drugs called aminoguanidine derivatives. It is an optically active compound and has an asymmetric carbon atom. The active enantiomer is 2-(2,3,4-trimethoxyphenyl)ethanamine and the inactive enantiomer is 2-(2,3,4-trimethoxyphenyl)ethylamine. This drug inhibits the activity of aldose reductase which converts glucose into sorbitol. Sorbitol accumulation then leads to diabetic complications such as cataracts and nerve damage. 2-(2,3,4-Trimethoxyphenyl)ethan-1-amine also inhibits platelet aggregation and thrombus formation by inhibiting the release of serotonin from platelets and preventing platelet adhesion to

Formula: C₁₁H₁₇NO₃

Purity: Min. 95%

Molecular weight: 211.26 g/mol

Ref: 3D-DAA93716