4-Bromo-5-iodo-2-methoxybenzoic acid

98%

Reagent Code: #130096
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CAS Number 1545259-60-6

science Other reagents with same CAS 1545259-60-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 356.94 g/mol
Formula C₈H₆BrIO₃
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MDL Number MFCD24189633
inventory_2 Storage & Handling
Storage Room temperature, away from light, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds requiring selective halogen substitution for enhanced reactivity or binding properties. Its functional groups allow for coupling reactions, such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for constructing complex aromatic systems. Also employed in the preparation of radiolabeled compounds for imaging studies due to the presence of iodine, which can be substituted with radioactive isotopes. The carboxylic acid group enables esterification or amide formation, facilitating incorporation into larger bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,900.00
inventory 250mg
10-20 days ฿21,410.00

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4-Bromo-5-iodo-2-methoxybenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds requiring selective halogen substitution for enhanced reactivity or binding properties. Its functional groups allow for coupling reactions, such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for constructing complex aromatic systems. Also employed in the preparation of radiolabeled compounds for imaging studies due to the presence of iodine, which can be sub

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds requiring selective halogen substitution for enhanced reactivity or binding properties. Its functional groups allow for coupling reactions, such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for constructing complex aromatic systems. Also employed in the preparation of radiolabeled compounds for imaging studies due to the presence of iodine, which can be substituted with radioactive isotopes. The carboxylic acid group enables esterification or amide formation, facilitating incorporation into larger bioactive molecules.

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