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CS-W001157 4
Total: USD 88.00

2-(2,3-Dihydrobenzofuran-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

  • CAS No. 445303-12-8

  • Cat. No. CS-W019296
  • Purity≥97%
  • MDL No.MFCD10699453
  • HazMat Fee +

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    Each bottle is packed as an Excepted Quantity, with a maximum of 1g for items in class 6.1 packing group I or II, and up to 25g for all other hazardous materials.

    If shipping is charged to your FedEx account, the HazMat fee will be billed directly by the courier. Otherwise, the fee will be included on your invoice. To help you avoid the HazMat fee, we can package a 5g order of a class 6.1 packing group I or II material as five separate 1g units, and a 100g order of any other dangerous good as four 25g units. This packaging adjustment will be made unless you instruct otherwise on your purchase order. Below, you will find the fee schedule from FedEx for handling hazardous materials.

    Type
    HazMat Fee
    Excepted Quantity $0.00
    FedEx Limited Quantities Ground $0.00
    Hazmat Ground shipping $50.00+
    Inaccessible (Haz class 6.1 or 9), Domestic $68.00+
    Accessible (Haz class 3, 4, 5 or 8), Domestic $158.00+
    Inaccessible (Haz class 6.1 or 9), International $108.00+
    Accessible (Haz class 3, 4, 5 or 8), International $238.00+

    An item is classified as a dangerous good if our website displays Hazardous Material (HazMat) information for it.

    There is a HazMat shipping fee for each item that qualifies as a dangerous good. Please contact our quotation team via email to confirm the details.

*For research and further manufacturing use only, not for direct human use.

2-(2,3-Dihydrobenzofuran-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane|CS-W019296

Structure of 445303-12-8

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Description

This boronate ester features a 2,3-dihydrobenzofuran scaffold that enhances solubility and stability in aqueous and protic media. The tetramethyl-substituted dioxaborolane ring enables efficient Suzuki-Miyaura coupling under mild conditions, while the fused heterocyclic system imparts unique electronic and steric profiles. Ideal for constructing complex biaryl architectures in medicinal chemistry and materials synthesis.

Application

2-(2,3-Dihydrobenzofuran-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. Its dihydrobenzofuran moiety provides structural relevance to bioactive heterocycles, while the tetramethyl-substituted dioxaborolane enhances stability and functional group tolerance. The compound facilitates efficient C–C bond formation under mild conditions, enabling straightforward access to complex arylated scaffolds in medicinal chemistry and materials synthesis.

General Information

  • CAS No. 445303-12-8
  • Cat. No. CS-W019296
  • Purity ≥97%
  • MDL No. MFCD10699453
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₁₉BO₃
  • Molecular Weight 246.11
  • Synonym(s) 2-(2,3-dihydro-1-benzofuran-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • SMILES CC1(C)C(C)(C)OB(C2=CC=C3CCOC3=C2)O1

Computational Chemistry Data

  • TPSA   27.69
  • LogP   1.9207
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   1

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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