(2-iodo-5-methylphenyl)methanol

98%

Reagent Code: #199859
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CAS Number 220991-50-4

science Other reagents with same CAS 220991-50-4

blur_circular Chemical Specifications

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Weight 248.06 g/mol
Formula C₈H₉IO
badge Registry Numbers
MDL Number MFCD18397811
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of thyroid hormone analogs and radiolabeled compounds for medical imaging. Its iodine functionality allows for easy incorporation of radioactive isotopes, making it valuable in developing diagnostic agents for thyroid disorders. Also utilized in organic synthesis to build complex aromatic structures through cross-coupling reactions or as a building block in the development of bioactive molecules. The hydroxyl group enables further derivatization, such as esterification or ether formation, supporting its role in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,030.00
inventory 250mg
10-20 days ฿10,250.00
inventory 1g
10-20 days ฿33,900.00

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(2-iodo-5-methylphenyl)methanol
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Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of thyroid hormone analogs and radiolabeled compounds for medical imaging. Its iodine functionality allows for easy incorporation of radioactive isotopes, making it valuable in developing diagnostic agents for thyroid disorders. Also utilized in organic synthesis to build complex aromatic structures through cross-coupling reactions or as a building block in the development of bioactive molecules. The

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of thyroid hormone analogs and radiolabeled compounds for medical imaging. Its iodine functionality allows for easy incorporation of radioactive isotopes, making it valuable in developing diagnostic agents for thyroid disorders. Also utilized in organic synthesis to build complex aromatic structures through cross-coupling reactions or as a building block in the development of bioactive molecules. The hydroxyl group enables further derivatization, such as esterification or ether formation, supporting its role in medicinal chemistry research.

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