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CS-W001157 4
Total: USD 88.00

Methyl 3,5-dihydroxy-4-iodobenzoate

  • CAS No. 338454-02-7

  • Cat. No. CS-0090457
  • Purity≥96%
  • MDL No.MFCD15071424
  • 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.

Methyl 3,5-dihydroxy-4-iodobenzoate|CS-0090457

Structure of 338454-02-7

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Description

Methyl 3,5-dihydroxy-4-iodobenzoate features a benzene ring bearing strategically positioned hydroxyl groups and a terminal iodide, enabling direct functionalization in cross-coupling reactions. The methyl ester facilitates downstream derivatization, while the electron-rich aromatic core supports efficient metal-catalyzed transformations under mild conditions.

Application

Methyl 3,5-dihydroxy-4-iodobenzoate serves as a versatile building block for the synthesis of bioactive heterocycles and functionalized aromatic scaffolds. The ortho-dihydroxy motif enables metal-catalyzed coupling reactions, while the iodide group facilitates palladium-catalyzed cross-couplings under mild conditions. Bench-stable and amenable to orthogonal functional group manipulation, it supports efficient access to complex phenolic architectures in medicinal chemistry and materials science applications.

General Information

  • CAS No. 338454-02-7
  • Cat. No. CS-0090457
  • Purity ≥96%
  • MDL No. MFCD15071424
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₇IO₄
  • Molecular Weight 294.04
  • Synonym(s) None
  • SMILES O=C(OC)C1=CC(O)=C(I)C(O)=C1

Computational Chemistry Data

  • TPSA   66.76
  • LogP   1.489
  • H_Acceptors   4
  • H_Donors   2
  • 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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