897035-07-3 Usage
Chemical class
Tetrahydroisoquinolines
1-(2-HYDROXYNAPHTH-1-YL)-6,7-DIMETHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE belongs to a class of organic compounds that have a core structure of an isoquinoline with a partially saturated ring.
Derivative of
Naphthyl
The compound is derived from naphthyl, which is a fused aromatic ring system consisting of two benzene rings.
Functional groups
Hydroxyl and methoxy groups
The compound contains a hydroxyl (-OH) group at the 2-position of the naphthyl ring and two methoxy (-OCH3) groups at the 6 and 7 positions of the isoquinoline ring.
Potential applications
Medicinal chemistry and pharmacology
Due to its structural properties and potential biological activities, 1-(2-HYDROXYNAPHTH-1-YL)-6,7-DIMETHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE may have applications in the development of new drugs and therapies.
Dopamine receptor interaction
Agonist or antagonist
The compound may have the potential to act as a dopamine receptor agonist or antagonist, which could be useful in treating conditions related to dopamine dysregulation.
Effects on neurotransmitter systems
Possible modulation
In addition to its potential interaction with dopamine receptors, the compound may also have effects on other neurotransmitter systems, which could contribute to its pharmacological properties.
Further research needed
Pharmacological and medicinal properties
More research is required to fully understand the compound's pharmacological effects, medicinal potential, and any potential side effects or limitations in its use.
Check Digit Verification of cas no
The CAS Registry Mumber 897035-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,7,0,3 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 897035-07:
(8*8)+(7*9)+(6*7)+(5*0)+(4*3)+(3*5)+(2*0)+(1*7)=203
203 % 10 = 3
So 897035-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C21H21NO3/c1-24-18-11-14-9-10-22-21(16(14)12-19(18)25-2)20-15-6-4-3-5-13(15)7-8-17(20)23/h3-8,11-12,21-23H,9-10H2,1-2H3
897035-07-3Relevant academic research and scientific papers
Synthesis and conformational analysis of naphth[1,2-e][1,3]oxazino[4,3-a][1,3]isoquinoline and naphth[2,1-e][1,3]oxazino[4,3-a]isoquinoline derivatives
Heydenreich, Matthias,Koch, Andreas,Szatmári, István,Fül?p, Ferenc,Kleinpeter, Erich
, p. 7378 - 7385 (2008/12/20)
Through the cyclization of 1-(β-hydroxynaphthyl)-1,2,3,4-tetrahydroisoquinoline and 1-(α-hydroxynaphthyl)-1,2,3,4-tetrahydroisoquinoline with formaldehyde, phosgene, p-nitrobenzaldehyde or p-chlorophenyl isothiocyanate, 8-substituted 10,11-dihydro-8H,15bH
Microwave-assisted, solvent-free synthesis of 1-(α- or β-hydroxynaphthyl)-1,2,3,4-tetrahydroisoquinolines by the Mannich reaction
Szatmári, István,Lázár, László,Fül?p, Ferenc
, p. 3881 - 3883 (2007/10/03)
As a new extension of the Mannich reaction of naphthols, 1-(hydroxynaphthyl)-substituted 1,2,3,4-tetrahydroisoquinolines were synthesized by the nucleophilic addition of 1- or 2-naphthol to 3,4-dihydroisoquinolines under solvent-free conditions, using microwave irradiation. The additions to 3-methyl-6,7-dimethoxy-3,4-dihydroisoquinoline proved to be a highly diastereoselective processes, resulting in the cis isomers as the main or the only products.
