2,3-Difluorobenzoyl chloride

97%

Reagent Code: #57836
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Alias 2,3-Difluorobenzoyl chloride
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CAS Number 18355-73-2

science Other reagents with same CAS 18355-73-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.55 g/mol
Formula F₂C₆H₃COCl
badge Registry Numbers
MDL Number MFCD00042499
thermostat Physical Properties
Boiling Point 85-87 °C/14 mmHg(lit.)
inventory_2 Storage & Handling
Density 1.423 g/mL at 25 °C(lit.)
Storage room temperature

description Product Description

Used primarily in organic synthesis, it serves as a key intermediate for producing pharmaceuticals and agrochemicals. It is particularly valuable in the creation of complex molecules due to its reactive benzoyl chloride group, which facilitates acylation reactions. Additionally, it is employed in the development of liquid crystal materials for electronic displays, leveraging its fluorine substituents to enhance thermal and chemical stability. Its role in the synthesis of specialty chemicals and advanced materials highlights its versatility in industrial applications.

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Test Parameter Specification
Purity 96.5-100%
Appearance Colorless to yellow liquid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,600.00
inventory 1g
10-20 days ฿1,380.00

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2,3-Difluorobenzoyl chloride
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Used primarily in organic synthesis, it serves as a key intermediate for producing pharmaceuticals and agrochemicals. It is particularly valuable in the creation of complex molecules due to its reactive benzoyl chloride group, which facilitates acylation reactions. Additionally, it is employed in the development of liquid crystal materials for electronic displays, leveraging its fluorine substituents to enhance thermal and chemical stability. Its role in the synthesis of specialty chemicals and advanced

Used primarily in organic synthesis, it serves as a key intermediate for producing pharmaceuticals and agrochemicals. It is particularly valuable in the creation of complex molecules due to its reactive benzoyl chloride group, which facilitates acylation reactions. Additionally, it is employed in the development of liquid crystal materials for electronic displays, leveraging its fluorine substituents to enhance thermal and chemical stability. Its role in the synthesis of specialty chemicals and advanced materials highlights its versatility in industrial applications.

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