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CAS

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146471-75-2

(1R,3R)-2-benzyl-5-(5-hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol is a complex organic compound characterized by a tetrahydroisoquinolinol core structure, a benzyl group, and hydroxy and methoxy substituents. This specific arrangement of atoms and functional groups endows the molecule with unique properties and potential biological activities, making it a promising candidate for pharmaceutical and medicinal chemistry applications.

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  • 146471-75-2 Structure

  • Basic information

    1. Product Name: (1R,3R)-2-benzyl-5-(5-hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol
    2. Synonyms: 8-isoquinolinol, 1,2,3,4-tetrahydro-5-(5-hydroxy-4-methoxy-2-methyl-1-naphthalenyl)-1,3-dimethyl-2-(phenylmethyl)-, (1R,3R)-
    3. CAS NO:146471-75-2
    4. Molecular Formula: C30H31NO3
    5. Molecular Weight: 453.572
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146471-75-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 575.553°C at 760 mmHg
    3. Flash Point: 301.884°C
    4. Appearance: N/A
    5. Density: 1.187g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.643
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (1R,3R)-2-benzyl-5-(5-hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol(CAS DataBase Reference)
    11. NIST Chemistry Reference: (1R,3R)-2-benzyl-5-(5-hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol(146471-75-2)
    12. EPA Substance Registry System: (1R,3R)-2-benzyl-5-(5-hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol(146471-75-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 146471-75-2(Hazardous Substances Data)

146471-75-2 Usage

Uses

Used in Pharmaceutical Industry:
(1R,3R)-2-benzyl-5-(5-hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol is used as a pharmaceutical agent for its potential therapeutic effects. (1R,3R)-2-benzyl-5-(5-hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol's unique structure and functional groups may contribute to its interaction with biological targets, such as receptors, enzymes, or other proteins, leading to potential applications in the treatment of various diseases or conditions.
Used in Medicinal Chemistry Research:
(1R,3R)-2-benzyl-5-(5-hydroxy-4-methoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol serves as a valuable compound in medicinal chemistry research. Its specific properties and potential biological activities make it an interesting subject for studying the structure-activity relationship, optimization of drug candidates, and the discovery of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 146471-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,4,7 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 146471-75:
(8*1)+(7*4)+(6*6)+(5*4)+(4*7)+(3*1)+(2*7)+(1*5)=142
142 % 10 = 2
So 146471-75-2 is a valid CAS Registry Number.

146471-75-2Downstream Products

146471-75-2Relevant articles and documents

First synthesis of the antimalarial naphthylisoquinoline alkaloid dioncophylline C, and its unnatural anti-HIV dimer, jozimine C1

Bringmann, Gerhard,Holenz, Joerg,Weirich, Ralf,Ruebenacker, Martin,Funke, Christian,Boyd, Michael R.,Gulakowski, Robert J.,Francois, Guido

, p. 497 - 512 (1998)

The first total synthesis of dioncophylline C, a new antimalarial lead structure, is described. For the directed construction of the stereogenic biaryl axis, the 'lactone methodology' is applied, despite the lack of a 'bridgehead oxygen' function in the t

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