2-(5-Formylthiophen-2-yl)benzonitrile

95%

Reagent Code: #41754
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CAS Number 194416-92-7

science Other reagents with same CAS 194416-92-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.26 g/mol
Formula C₁₂H₇NOS
badge Registry Numbers
MDL Number MFCD06740277
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the synthesis of organic compounds, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring both a formyl group and a nitrile group, makes it a versatile intermediate in organic reactions. It is often employed in the construction of heterocyclic compounds, which are crucial in drug discovery and development. Additionally, it serves as a building block in the production of materials with potential applications in organic electronics and optoelectronics, such as organic light-emitting diodes (OLEDs) and photovoltaic cells. Its reactivity also allows for its use in coupling reactions, contributing to the creation of complex molecules with specific functional properties.

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Test Parameter Specification
Purity 94.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,872.00
inventory 250mg
10-20 days ฿19,818.00

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2-(5-Formylthiophen-2-yl)benzonitrile
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This chemical is primarily utilized in the synthesis of organic compounds, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring both a formyl group and a nitrile group, makes it a versatile intermediate in organic reactions. It is often employed in the construction of heterocyclic compounds, which are crucial in drug discovery and development. Additionally, it serves as a building block in the production of materials with potential applications in organic electro

This chemical is primarily utilized in the synthesis of organic compounds, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring both a formyl group and a nitrile group, makes it a versatile intermediate in organic reactions. It is often employed in the construction of heterocyclic compounds, which are crucial in drug discovery and development. Additionally, it serves as a building block in the production of materials with potential applications in organic electronics and optoelectronics, such as organic light-emitting diodes (OLEDs) and photovoltaic cells. Its reactivity also allows for its use in coupling reactions, contributing to the creation of complex molecules with specific functional properties.

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