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2-(2-(2-Chloroethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boronic ester chemical compound characterized by a chlorine-substituted phenyl group and four methyl groups attached to the boron atom. It is utilized in organic synthesis for the introduction of the boronic acid functionality into organic molecules, making it a valuable reagent in medicinal chemistry and material science for the development of new drugs and materials.

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  • 2-(2-(2-CHLOROETHOXY)PHENYL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE

    Cas No: 1256359-02-0

  • USD $ 1.9-2.9 / Gram

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  • 1256359-02-0 Structure
  • Basic information

    1. Product Name: 2-[2-(2-Chloroethoxy)phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
    2. Synonyms: 2-(2-Chloroethoxy)phenylboronic acid, pinacol ester;2-[2-(2-Chloroethoxy)phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane;2-(2-Chloro-ethoxy)-phenyl-4,4,5,5-tetraMethyl-1,3,2dioxaborolane
    3. CAS NO:1256359-02-0
    4. Molecular Formula: C14H20BClO3
    5. Molecular Weight: 282.5708
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1256359-02-0.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.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[2-(2-Chloroethoxy)phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[2-(2-Chloroethoxy)phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(1256359-02-0)
    11. EPA Substance Registry System: 2-[2-(2-Chloroethoxy)phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(1256359-02-0)
  • 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: 1256359-02-0(Hazardous Substances Data)

1256359-02-0 Usage

Uses

Used in Organic Synthesis:
2-(2-(2-Chloroethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a reagent for the introduction of the boronic acid functionality into organic molecules, facilitating the synthesis of various organic compounds.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 2-(2-(2-Chloroethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a key intermediate in the development of new drugs, owing to its ability to form stable boron-containing compounds with potential therapeutic properties.
Used in Material Science:
2-(2-(2-Chloroethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is employed as a precursor in the synthesis of advanced materials with unique properties, such as boron-containing polymers and nanomaterials, for various applications in material science.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
In the production of fine chemicals and pharmaceuticals, 2-(2-(2-Chloroethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a coupling partner in Suzuki-Miyaura cross-coupling reactions, a widely used method for the formation of carbon-carbon bonds, enabling the synthesis of complex molecular structures with high selectivity and efficiency.

Check Digit Verification of cas no

The CAS Registry Mumber 1256359-02-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,5 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1256359-02:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*5)+(3*9)+(2*0)+(1*2)=160
160 % 10 = 0
So 1256359-02-0 is a valid CAS Registry Number.

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