(1-(Trifluoromethyl)cyclobutyl)methanol

98%

Reagent Code: #238377
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CAS Number 371917-16-7

science Other reagents with same CAS 371917-16-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.13 g/mol
Formula C₆H₉OF₃
badge Registry Numbers
MDL Number MFCD28383968
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules where the trifluoromethyl group enhances metabolic stability and lipophilicity. Its structure is valuable in medicinal chemistry for optimizing drug candidates targeting central nervous system disorders and inflammatory diseases. The alcohol functionality allows for easy derivatization, enabling attachment to larger molecular frameworks through ester, ether, or carbamate linkages. Also employed in agrochemical research for designing novel pesticides with improved environmental persistence and target selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,680.00
inventory 250mg
10-20 days ฿13,120.00
inventory 500mg
10-20 days ฿21,920.00
inventory 1g
10-20 days ฿35,200.00
(1-(Trifluoromethyl)cyclobutyl)methanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules where the trifluoromethyl group enhances metabolic stability and lipophilicity. Its structure is valuable in medicinal chemistry for optimizing drug candidates targeting central nervous system disorders and inflammatory diseases. The alcohol functionality allows for easy derivatization, enabling attachment to larger molecular frameworks through ester, ether, or carbamate linkages. Also e

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules where the trifluoromethyl group enhances metabolic stability and lipophilicity. Its structure is valuable in medicinal chemistry for optimizing drug candidates targeting central nervous system disorders and inflammatory diseases. The alcohol functionality allows for easy derivatization, enabling attachment to larger molecular frameworks through ester, ether, or carbamate linkages. Also employed in agrochemical research for designing novel pesticides with improved environmental persistence and target selectivity.

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