(2-Iodo-4-(trifluoromethyl)phenyl)methanol

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Reagent Code: #36448
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CAS Number 873005-49-3

science Other reagents with same CAS 873005-49-3

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Weight 302.0400 g/mol
Formula C₈H₆F₃IO
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MDL Number MFCD18398172
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(2-Iodo-4-(trifluoromethyl)phenyl)methanol is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its structure, featuring both an iodine substituent and a trifluoromethyl group, makes it valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The iodine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in creating biologically active molecules. The trifluoromethyl group enhances the lipophilicity and metabolic stability of the resulting compounds, making it particularly useful in drug discovery. Additionally, this compound can serve as a building block in the synthesis of liquid crystals or materials for organic electronics due to its unique electronic properties.

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inventory 100mg
10-20 days ฿2,187.00

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(2-Iodo-4-(trifluoromethyl)phenyl)methanol
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(2-Iodo-4-(trifluoromethyl)phenyl)methanol is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its structure, featuring both an iodine substituent and a trifluoromethyl group, makes it valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The iodine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in creating biolo

(2-Iodo-4-(trifluoromethyl)phenyl)methanol is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its structure, featuring both an iodine substituent and a trifluoromethyl group, makes it valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The iodine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in creating biologically active molecules. The trifluoromethyl group enhances the lipophilicity and metabolic stability of the resulting compounds, making it particularly useful in drug discovery. Additionally, this compound can serve as a building block in the synthesis of liquid crystals or materials for organic electronics due to its unique electronic properties.

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