2-Amino-5-iodo-4-methoxybenzoic acid

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Reagent Code: #137876
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CAS Number 1335203-40-1

science Other reagents with same CAS 1335203-40-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.059 g/mol
Formula C₈H₈NO₃I
badge Registry Numbers
MDL Number MFCD28968035
thermostat Physical Properties
Boiling Point 408.1±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.949±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof storage, dry seal

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of thyroid hormone analogs and radiolabeled compounds for medical imaging. Its iodine content makes it valuable in radioiodination studies, where it serves as a precursor for creating tracers used in diagnostic applications. Also utilized in organic synthesis to build complex heterocyclic systems due to the presence of both amino and carboxylic acid functional groups, enabling coupling reactions and ring formation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,080.00
inventory 250mg
10-20 days ฿5,150.00
inventory 1g
10-20 days ฿12,870.00

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2-Amino-5-iodo-4-methoxybenzoic acid
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of thyroid hormone analogs and radiolabeled compounds for medical imaging. Its iodine content makes it valuable in radioiodination studies, where it serves as a precursor for creating tracers used in diagnostic applications. Also utilized in organic synthesis to build complex heterocyclic systems due to the presence of both amino and carboxylic acid functional groups, enabling coupling reactions and ring formation.

Used in the synthesis of pharmaceutical intermediates, particularly in the development of thyroid hormone analogs and radiolabeled compounds for medical imaging. Its iodine content makes it valuable in radioiodination studies, where it serves as a precursor for creating tracers used in diagnostic applications. Also utilized in organic synthesis to build complex heterocyclic systems due to the presence of both amino and carboxylic acid functional groups, enabling coupling reactions and ring formation.

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