Boron trifluoride tetrahydrofuran complex

48-50% solution

Reagent Code: #143062
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Alias Boron trifluoride tetrahydrofuran complex; Boron trifluoride tetrahydrofuran
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CAS Number 462-34-0

science Other reagents with same CAS 462-34-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.91 g/mol
Formula BF₃·C₄H₈O
badge Registry Numbers
EC Number 207-325-9
MDL Number MFCD00040372
thermostat Physical Properties
Melting Point −123 °C(lit.)
Boiling Point 180 °C(lit.)
inventory_2 Storage & Handling
Density 1.268 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a versatile Lewis acid catalyst in organic synthesis, particularly in alkylation, acylation, polymerization, Diels-Alder, and Friedel-Crafts reactions. Commonly employed in the preparation of pharmaceuticals, agrochemicals, fine chemicals, and in carbohydrate synthesis for glycoside bond formation due to its stability and solubility in organic solvents. Facilitates ring-opening reactions of epoxides to yield aldehydes or ketones and promotes efficient C-C bond formation. Its complexation with tetrahydrofuran enhances handling, stability, and reactivity control compared to gaseous boron trifluoride, making it popular in laboratory and industrial organic chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100ml
10-20 days ฿610.00
inventory 500ml
10-20 days ฿2,140.00
inventory 2.5L
10-20 days ฿8,560.00
inventory 10L
10-20 days ฿31,900.00

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Boron trifluoride tetrahydrofuran complex
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Used as a versatile Lewis acid catalyst in organic synthesis, particularly in alkylation, acylation, polymerization, Diels-Alder, and Friedel-Crafts reactions. Commonly employed in the preparation of pharmaceuticals, agrochemicals, fine chemicals, and in carbohydrate synthesis for glycoside bond formation due to its stability and solubility in organic solvents. Facilitates ring-opening reactions of epoxides to yield aldehydes or ketones and promotes efficient C-C bond formation. Its complexation with tet

Used as a versatile Lewis acid catalyst in organic synthesis, particularly in alkylation, acylation, polymerization, Diels-Alder, and Friedel-Crafts reactions. Commonly employed in the preparation of pharmaceuticals, agrochemicals, fine chemicals, and in carbohydrate synthesis for glycoside bond formation due to its stability and solubility in organic solvents. Facilitates ring-opening reactions of epoxides to yield aldehydes or ketones and promotes efficient C-C bond formation. Its complexation with tetrahydrofuran enhances handling, stability, and reactivity control compared to gaseous boron trifluoride, making it popular in laboratory and industrial organic chemistry.

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