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4-(6,7-DIMETHOXY-1,2,3,4-TETRAHYDRO-ISOQUINOLIN-1-YL)-PHENOL is a chemical compound characterized by a phenol group connected to a tetrahydroisoquinoline ring, which is further substituted with two methoxy groups. This unique structure endows it with potential pharmacological properties, making it a promising candidate for medicinal chemistry research. The tetrahydroisoquinoline ring suggests that it may have biological effects related to neurotransmission or other physiological processes influenced by similar compounds.

301325-93-9

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301325-93-9 Usage

Uses

Used in Pharmaceutical Research:
4-(6,7-DIMETHOXY-1,2,3,4-TETRAHYDRO-ISOQUINOLIN-1-YL)-PHENOL is used as a research compound for exploring its potential pharmacological activity. The presence of the tetrahydroisoquinoline ring indicates that it may have applications in modulating neurotransmission or other physiological processes, warranting further investigation into its properties and efficacy.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-(6,7-DIMETHOXY-1,2,3,4-TETRAHYDRO-ISOQUINOLIN-1-YL)-PHENOL is utilized as a starting point for the development of new drugs. Its unique structure and potential biological effects make it a valuable tool for designing and synthesizing novel therapeutic agents that could target specific physiological pathways or diseases.
Used in Neurotransmission Research:
4-(6,7-DIMETHOXY-1,2,3,4-TETRAHYDRO-ISOQUINOLIN-1-YL)-PHENOL is used as a research tool in the study of neurotransmission. Its tetrahydroisoquinoline ring may confer properties that allow it to interact with neurotransmitter systems, providing insights into the development of drugs that could modulate these systems for the treatment of neurological disorders.
Used in Drug Design and Synthesis:
In the process of drug design and synthesis, 4-(6,7-DIMETHOXY-1,2,3,4-TETRAHYDRO-ISOQUINOLIN-1-YL)-PHENOL serves as a key intermediate or building block. Its unique structure can be further modified or combined with other chemical entities to create new compounds with enhanced pharmacological properties or improved drug delivery characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 301325-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,1,3,2 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 301325-93:
(8*3)+(7*0)+(6*1)+(5*3)+(4*2)+(3*5)+(2*9)+(1*3)=89
89 % 10 = 9
So 301325-93-9 is a valid CAS Registry Number.

301325-93-9Relevant academic research and scientific papers

Synthesis of carbon-11 and fluorine-18 labeled N-acetyl-1-aryl-6,7- dimethoxy-1,2,3,4-tetrahydroisoquinoline derivatives as new potential PET AMPA receptor ligands

Gao, Mingzhang,Kong, Deyuan,Clearfield, Abraham,Zheng, Qi-Huang

, p. 2229 - 2233 (2007/10/03)

New carbon-11 and fluorine-18 labeled N-acetyl-1-aryl-6,7-dimethoxy-1,2,3, 4-tetrahydroisoquinoline derivatives were designed and synthesized as potential positron emission tomography AMPA (2-amino-3-(3-hydroxy-5-methylisoxazol-4-yl) propionic acid) recep

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