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1298044-31-1

(4R)-4-(6-bromo-2-methoxyquinolin-3-yl)-3-(naphthalen-1-yl)-4-phenylbutane-1,3-diol is a complex organic molecule featuring a quinoline ring with a bromine and methoxy group, a naphthalene ring, and a phenylbutane-1,3-diol group. This chiral compound, with a 4R configuration, comprises multiple aromatic and alcohol functional groups, which may contribute to its potential pharmaceutical or research applications due to its unique structure and the ability to interact with biological systems.

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  • (4R)-4-(6-bromo-2-methoxyquinolin-3-yl)-3-(naphthalen-1-yl)-4-phenylbutane-1,3-diol

    Cas No: 1298044-31-1

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  • 1298044-31-1 Structure

  • Basic information

    1. Product Name: (4R)-4-(6-bromo-2-methoxyquinolin-3-yl)-3-(naphthalen-1-yl)-4-phenylbutane-1,3-diol
    2. Synonyms: (4R)-4-(6-bromo-2-methoxyquinolin-3-yl)-3-(naphthalen-1-yl)-4-phenylbutane-1,3-diol
    3. CAS NO:1298044-31-1
    4. Molecular Formula:
    5. Molecular Weight: 528.445
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1298044-31-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (4R)-4-(6-bromo-2-methoxyquinolin-3-yl)-3-(naphthalen-1-yl)-4-phenylbutane-1,3-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4R)-4-(6-bromo-2-methoxyquinolin-3-yl)-3-(naphthalen-1-yl)-4-phenylbutane-1,3-diol(1298044-31-1)
    11. EPA Substance Registry System: (4R)-4-(6-bromo-2-methoxyquinolin-3-yl)-3-(naphthalen-1-yl)-4-phenylbutane-1,3-diol(1298044-31-1)

  • 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: 1298044-31-1(Hazardous Substances Data)

1298044-31-1 Usage

Uses

Used in Pharmaceutical Applications:
(4R)-4-(6-bromo-2-methoxyquinolin-3-yl)-3-(naphthalen-1-yl)-4-phenylbutane-1,3-diol is used as a potential pharmaceutical agent for its unique structure and functional groups that could be harnessed to target specific biological pathways or receptors. The presence of the quinoline ring, bromine and methoxy substitutions, naphthalene ring, and phenylbutane-1,3-diol group may allow for the modulation of various biological processes, making it a candidate for drug development.
Used in Research Applications:
In the field of research, (4R)-4-(6-bromo-2-methoxyquinolin-3-yl)-3-(naphthalen-1-yl)-4-phenylbutane-1,3-diol serves as a valuable compound for studying the interactions between small molecules and biological systems. Its chiral nature and diverse functional groups provide opportunities for investigating stereoselectivity and the influence of specific structural features on biological activity, which can be crucial for understanding mechanisms of action and optimizing drug design.
Further study and characterization of this chemical may reveal additional potential uses and properties, expanding its applications across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1298044-31-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,8,0,4 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1298044-31:
(9*1)+(8*2)+(7*9)+(6*8)+(5*0)+(4*4)+(3*4)+(2*3)+(1*1)=171
171 % 10 = 1
So 1298044-31-1 is a valid CAS Registry Number.

1298044-31-1Relevant articles and documents

Practical syntheses of (2S)-R207910 and (2R)-R207910

Chandrasekhar, Srivari,Babu, G. S. Kiran,Mohapatra, Debendra K.

, p. 2057 - 2061 (2011/05/09)

Concise and practical syntheses of (2S)-R207910 (3a) and (2R)-R207910 (3b) have been achieved in high overall yield of 12 % in 10 steps for each isomer starting from a known intermediate following Sharpless asymmetric epoxidation, regioselective epoxide opening, modified allylzinc bromide addition as key reactions. Copyright

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