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CS-W001157 4
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(3-Fluoro-5-(methoxycarbonyl)phenyl)boronic acid

  • CAS No. 871329-62-3

  • Cat. No. CS-0067554
  • Purity≥98%
  • MDL No.MFCD07363749
  • 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.

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

(3-Fluoro-5-(methoxycarbonyl)phenyl)boronic acid|CS-0067554

Structure of 871329-62-3

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Description

This boronic acid features a fluorinated aryl core paired with a methoxycarbonyl group, enabling selective coupling in Suzuki-Miyaura reactions. The electron-withdrawing fluorine enhances reactivity while the ester functionality offers tunable stability and compatibility under standard conditions.

Application

(3-Fluoro-5-(methoxycarbonyl)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The ortho-fluorine and ester functionalities provide orthogonal reactivity for downstream modifications, while the boronic acid moiety offers excellent bench stability and ease of purification. This compound is particularly valuable in constructing substituted heterocycles and biaryl architectures common in pharmaceutical synthesis.

General Information

  • CAS No. 871329-62-3
  • Cat. No. CS-0067554
  • Purity ≥98%
  • MDL No. MFCD07363749
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₈BFO₄
  • Molecular Weight 197.96
  • Synonym(s) 3-Fluoro-5-methoxycarbonylphenylboronic acid
  • SMILES OB(O)C1=CC(F)=CC(C(OC)=O)=C1

Computational Chemistry Data

  • TPSA   66.76
  • LogP   -0.7079
  • H_Acceptors   4
  • H_Donors   2
  • Rotatable_Bonds   2

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302
Precautionary Statements : P264-P270-P330-P501

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