1-(3-Iodophenyl)ethan-1-ol

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Reagent Code: #201039
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CAS Number 79917-56-9

science Other reagents with same CAS 79917-56-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.06 g/mol
Formula C₈H₉IO
badge Registry Numbers
MDL Number MFCD22573005
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and radiopharmaceuticals, particularly in the development of labeled compounds for medical imaging. Its iodine-containing aromatic structure makes 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 molecules where a functionalized iodophenyl scaffold is required. The hydroxyl group allows for further derivatization, enabling coupling reactions or esterification to modify pharmacokinetic properties in drug design.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,130.00
inventory 1g
10-20 days ฿8,890.00
inventory 5g
10-20 days ฿36,300.00

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1-(3-Iodophenyl)ethan-1-ol
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Used as an intermediate in the synthesis of pharmaceuticals and radiopharmaceuticals, particularly in the development of labeled compounds for medical imaging. Its iodine-containing aromatic structure makes 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 molecules where a functionalized iodophenyl scaffold is required. The hydroxyl group allows for further derivatization, ena

Used as an intermediate in the synthesis of pharmaceuticals and radiopharmaceuticals, particularly in the development of labeled compounds for medical imaging. Its iodine-containing aromatic structure makes 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 molecules where a functionalized iodophenyl scaffold is required. The hydroxyl group allows for further derivatization, enabling coupling reactions or esterification to modify pharmacokinetic properties in drug design.

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