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1-(4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N-dimethylmethanamine is an organic compound characterized by a fluoro-substituted phenyl ring, a dimethylamino group, and a methylene bridge. It also incorporates a boron-containing heterocyclic ring, specifically a dioxaborolane, which is commonly utilized in organic synthesis and medicinal chemistry. This unique structure and the presence of functional groups make it a promising candidate for pharmaceutical research and as a building block in chemical synthesis.

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  • 1-(4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N-dimethylmethanamine

    Cas No: 1431470-48-2

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  • 1431470-48-2 Structure
  • Basic information

    1. Product Name: 1-(4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N-dimethylmethanamine
    2. Synonyms: 1-(4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N-dimethylmethanamine;2-Fluoro-5-(dimethylaminomethyl)phenylboronic acid pinacol ester
    3. CAS NO:1431470-48-2
    4. Molecular Formula: C15H23BFNO2
    5. Molecular Weight: 279.1580232
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1431470-48-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: Room temperature.
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N-dimethylmethanamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N-dimethylmethanamine(1431470-48-2)
    11. EPA Substance Registry System: 1-(4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N-dimethylmethanamine(1431470-48-2)
  • 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: 1431470-48-2(Hazardous Substances Data)

1431470-48-2 Usage

Uses

Used in Pharmaceutical Research:
1-(4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N-dimethylmethanamine is used as a research compound for its potential applications in the development of new pharmaceuticals. Its unique structure and functional groups can be leveraged to design and synthesize novel drug molecules with specific therapeutic properties.
Used in Chemical Synthesis:
In the field of chemical synthesis, 1-(4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N-dimethylmethanamine serves as a valuable building block. Its fluoro-substituted phenyl ring and dimethylamino group, along with the boron-containing dioxaborolane ring, can be utilized in the synthesis of complex organic molecules and advanced materials.
Used in Organic Synthesis:
1-(4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N-dimethylmethanamine is used as a key intermediate in organic synthesis. Its versatile structure allows for further functionalization and modification, enabling the synthesis of a wide range of organic compounds with diverse applications.
Used in Medicinal Chemistry:
In medicinal chemistry, 1-(4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N-dimethylmethanamine is employed as a starting material or a synthetic intermediate for the development of new drugs. Its unique structural features and functional groups can be exploited to create bioactive molecules with potential therapeutic benefits.
Used in the Synthesis of Fluoro-containing Compounds:
Due to the presence of a fluoro-substituted phenyl ring, 1-(4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N-dimethylmethanamine is used in the synthesis of fluoro-containing compounds. Fluorinated compounds often exhibit unique chemical and biological properties, making them valuable in various applications, including pharmaceuticals, agrochemicals, and materials science.
Used in the Synthesis of Boron-containing Compounds:
The boron-containing dioxaborolane ring in 1-(4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N-dimethylmethanamine makes it a suitable candidate for the synthesis of boron-containing compounds. Boron compounds have a wide range of applications, including as catalysts, materials, and pharmaceutical agents.

Check Digit Verification of cas no

The CAS Registry Mumber 1431470-48-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,1,4,7 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1431470-48:
(9*1)+(8*4)+(7*3)+(6*1)+(5*4)+(4*7)+(3*0)+(2*4)+(1*8)=132
132 % 10 = 2
So 1431470-48-2 is a valid CAS Registry Number.

1431470-48-2Upstream product

1431470-48-2Downstream Products

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