2-Amino-6-(trifluoromethyl)benzyl alcohol

97%

Reagent Code: #133444
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CAS Number 763027-00-5

science Other reagents with same CAS 763027-00-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.1504 g/mol
Formula C₈H₈F₃NO
badge Registry Numbers
MDL Number MFCD11847528
thermostat Physical Properties
Boiling Point 265.7±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.374±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of central nervous system agents and anti-inflammatory drugs. Its trifluoromethyl group enhances metabolic stability and membrane permeability, making it valuable in medicinal chemistry. Also employed in the preparation of chiral ligands for asymmetric catalysis. The hydroxyl and amino functional groups allow for versatile derivatization in multi-step organic synthesis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿27,200.00
inventory 1g
10-20 days ฿60,800.00

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2-Amino-6-(trifluoromethyl)benzyl alcohol
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of central nervous system agents and anti-inflammatory drugs. Its trifluoromethyl group enhances metabolic stability and membrane permeability, making it valuable in medicinal chemistry. Also employed in the preparation of chiral ligands for asymmetric catalysis. The hydroxyl and amino functional groups allow for versatile derivatization in multi-step organic synthesis.

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of central nervous system agents and anti-inflammatory drugs. Its trifluoromethyl group enhances metabolic stability and membrane permeability, making it valuable in medicinal chemistry. Also employed in the preparation of chiral ligands for asymmetric catalysis. The hydroxyl and amino functional groups allow for versatile derivatization in multi-step organic synthesis.

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