91245-72-6

Usage

Uses

Due to the limited information available on 1,2,3,4-TETRAHYDRONAPHTHALEN-1-YLMETHYLAMINE, its applications are not well-defined. However, based on its chemical structure, it can be speculated that it may have potential uses in various industries, such as:
Used in Pharmaceutical Industry:
1,2,3,4-TETRAHYDRONAPHTHALEN-1-YLMETHYLAMINE could be used as an intermediate compound for the synthesis of pharmaceutical drugs, given its unique tetralin and methylamine structure. This could be beneficial for the development of new medications with specific therapeutic properties.
Used in Chemical Research:
1,2,3,4-TETRAHYDRONAPHTHALEN-1-YLMETHYLAMINE may be utilized as a research compound in academic or industrial laboratories, where its chemical properties and reactivity could be studied and potentially applied in the development of new chemical processes or materials.
Used in Material Science:
Given its unique structure, 1,2,3,4-TETRAHYDRONAPHTHALEN-1-YLMETHYLAMINE could potentially be used in the development of new materials with specific properties, such as improved conductivity, stability, or reactivity, depending on further research and development in this area.

Upstream product

• 155566-54-4 1,2,3,4-tetrahydro-1-naphthalenecarbaldehyde 
• 64-17-5 ethanol 
• 86-53-3 1-Cyanonaphthalene 
• 25108-63-8 1-methylene-1,2,3,4-tetrahydronaphthalene 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 50361-53-0 1-(trimethylsilyloxy)-1,2,3,4-tetrahydronaphthalene-1-carbonitrile 
• 92367-60-7 1-Oximino-formyl-tetralin 
• 80096-56-6 (+/-)-1-(aminomethyl)-1-hydroxy-1,2,3,4-tetrahydronaphthalene hydrochloride 
• 50361-60-9 1-aminomethyl-1-hydroxy-1,2,3,4-tetrahydronaphthalene 

Downstream Products

• 144-62-7 oxalic acid 
• 88-99-3 benzene-1,2-dicarboxylic acid 
• 98977-64-1 (E)-N-methyl-N-(3-phenyl-2-propenyl)-1,2,3,4-tetrahydro-1-naphthalenemethanamine 

Relevant academic research and scientific papers

Direct Access to Primary Amines from Alkenes by Selective Metal-Free Hydroamination

Direct and selective synthesis of primary amines from easily available precursors is attractive yet challenging. Herein, we report the rapid synthesis of primary amines from alkenes via metal-free regioselective hydroamination at room temperature. Ammonium carbonate was used as ammonia surrogate for the first time, allowing for efficient conversion of terminal and internal alkenes into linear, α-branched, and α-tertiary primary amines under mild conditions. This method provides a straightforward and powerful approach to a wide spectrum of advanced, highly functionalized primary amines which are of particular interest in pharmaceutical chemistry and other areas.

N6-Substituted Adenosine Receptor Agonists: Potential AntihypertensiveAgents

Adenosine is known to exert a wide range of pharmacological effects including hypotension.This effect of adenosine suggested that modified analogues of adenosine might provide useful antihypertensive agents.Thus, we prepared a series of novel N6/sup

Serotonin Receptor Affinity of Cathinone and Related Analogues

A series of cathinone (α-aminopropiophenone) analogues was examined using the isolated rat fundus preparation. (S)-(-)-Cathinone possesses twice the serotonin receptor affinity of (+/-)-cathinone and four times the affinity of racemic amphetamine.Several derivatives of cathinone were found to either possess a lower affinity than the parent compound or did not interact with the receptors in a competitive manner.Several novel analogues, 1-(aminomethyl)-3,4-dihydronaphthalene hydrochloride (3), 4-(aminomethyl)-3-chromene hydrochloride (4b), as well as its 6-methoxy derivative, 4a, interact with serotonin receptors but in a fashion which is, most likely, dissimilar to the interaction of the substituted cathinone analogues.