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  8. 3-Bromo-5-iodobenzoic acid, 97%, Thermo Scientific Chemicals

3-Bromo-5-iodobenzoic acid, 97%, Thermo Scientific Chemicals

Catalog Number p-7023482
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Quantity:
5 g
25 g
100 g
This item is not returnable. View return policy
188815-32-9
C7H4BrIO2
326.915
MFCD00191851
MKJBJYCBKXPQSY-UHFFFAOYSA-N
5-bromo-3-iodobenzoic acid, 3-bromo-5-iodo-benzoic acid, 3-bromo-5-iodobenzoicacid, benzoic acid, 3-bromo-5-iodo, 3-iodo-5-bromobenzoic acid, pubchem3788, acmc-209erv, 3-bromo-5-iodobenzoic aicd, 3-bromo-5-iodo benzoic acid, 5-iodo-3-bromo-benzoic acid
5182520
3-bromo-5-iodobenzoic acid
C1=C(C=C(C=C1Br)I)C(=O)O
This item is not returnable. View return policy
188815-32-9
C7H4BrIO2
326.915
MFCD00191851
MKJBJYCBKXPQSY-UHFFFAOYSA-N
5-bromo-3-iodobenzoic acid, 3-bromo-5-iodo-benzoic acid, 3-bromo-5-iodobenzoicacid, benzoic acid, 3-bromo-5-iodo, 3-iodo-5-bromobenzoic acid, pubchem3788, acmc-209erv, 3-bromo-5-iodobenzoic aicd, 3-bromo-5-iodo benzoic acid, 5-iodo-3-bromo-benzoic acid
5182520
3-bromo-5-iodobenzoic acid
C1=C(C=C(C=C1Br)I)C(=O)O

Description

3-Bromo-5-iodobenzoic acid may be used in the preparation of the following:

  • Phenyl(3-bromo-5-iodo)benzoate.
  • As starting reagent for the large-scale synthesis of the thromboxane receptor antagonist 3-{3-[2-(4-chlorobenzenesulfonamido)ethyl]-5-(4-fluorobenzyl)phenyl}propionic acid, via regioselective Heck cross-coupling reaction.
  • Methyl 3-bromo-5-iodobenzoate.
  • 3-Bromo-5-(triisopropylsilylethynyl)benzoic acid, via Sonogashira coupling reaction.
  • Trifluoroacetophenone.

    This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

    Applications
    3-Bromo-5-iodobenzoic acid may be used in the preparation of the following: • Phenyl(3-bromo-5-iodo)benzoate. • As starting reagent for the large-scale synthesis of the thromboxane receptor antagonist 3-{3-[2-(4-chlorobenzenesulfonamido)ethyl]-5-(4-fluorobenzyl)phenyl}propionic acid, via regioselective Heck cross-coupling reaction. • Methyl 3-bromo-5-iodobenzoate. • 3-Bromo-5-(triisopropylsilylethynyl)benzoic acid, via Sonogashira coupling reaction. • Trifluoroacetophenone.

    Solubility
    Soluble in methanol. Sparingly Soluble (0.20 g/L) (25°C), Calc.

    Notes
    Light Sensitive. Protect from light. Store away from oxidizing agents.
    TRUSTED_SUSTAINABILITY
    Melting Point 218°C to 221°C
    Quantity 5 g
    Beilstein 3240837
    Sensitivity Light sensitive
    Solubility Information Soluble in methanol. Sparingly Soluble (0.20g/L) (25°C),Calc.
    Formula Weight 326.92
    Percent Purity 97%
    Chemical Name or Material 3-Bromo-5-iodobenzoic acid

    RUO – Research Use Only

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