(4-Chlorophenyl)diphenylmethanol

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Reagent Code: #131181
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CAS Number 6922-89-0

science Other reagents with same CAS 6922-89-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.78 g/mol
Formula C₁₉H₁₅ClO
badge Registry Numbers
MDL Number MFCD00092575
thermostat Physical Properties
Melting Point 85 °C
Boiling Point 440.5±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.216±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antihistamines and anti-allergic agents. It serves as a building block in organic reactions where a triarylmethanol structure is required. Its chlorinated aromatic ring allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for developing bioactive molecules. Also employed in the preparation of ligands for catalysts in asymmetric synthesis.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿15,660.00
inventory 25mg
10-20 days ฿9,220.00

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(4-Chlorophenyl)diphenylmethanol
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antihistamines and anti-allergic agents. It serves as a building block in organic reactions where a triarylmethanol structure is required. Its chlorinated aromatic ring allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for developing bioactive molecules. Also employed in the preparation of ligands for catalysts in asymmetric synthesis.
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antihistamines and anti-allergic agents. It serves as a building block in organic reactions where a triarylmethanol structure is required. Its chlorinated aromatic ring allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for developing bioactive molecules. Also employed in the preparation of ligands for catalysts in asymmetric synthesis.
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