3-Iodo-2-methoxybenzoic acid

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Reagent Code: #131444
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CAS Number 879498-16-5

science Other reagents with same CAS 879498-16-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.04 g/mol
Formula C₈H₇IO₃
badge Registry Numbers
MDL Number MFCD18904882
thermostat Physical Properties
Melting Point 122-124 °C
Boiling Point 361.4±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.878±0.06 g/cm3(Predicted)
Storage Room temperature, away from light, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of radiolabeled compounds for medical imaging. Its structure allows for easy incorporation of iodine isotopes, making it valuable in creating tracers for positron emission tomography (PET) and single-photon emission computed tomography (SPECT). Also employed in organic synthesis to build complex aromatic molecules, especially in the preparation of bioactive compounds and functionalized benzoic acid derivatives.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,930.00
inventory 250mg
10-20 days ฿22,620.00

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3-Iodo-2-methoxybenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of radiolabeled compounds for medical imaging. Its structure allows for easy incorporation of iodine isotopes, making it valuable in creating tracers for positron emission tomography (PET) and single-photon emission computed tomography (SPECT). Also employed in organic synthesis to build complex aromatic molecules, especially in the preparation of bioactive compounds and functionalized benzoic acid derivatives.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of radiolabeled compounds for medical imaging. Its structure allows for easy incorporation of iodine isotopes, making it valuable in creating tracers for positron emission tomography (PET) and single-photon emission computed tomography (SPECT). Also employed in organic synthesis to build complex aromatic molecules, especially in the preparation of bioactive compounds and functionalized benzoic acid derivatives.

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