ethyl 9H-carbazole-2-carboxylate

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Reagent Code: #84260
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CAS Number 82408-83-1

science Other reagents with same CAS 82408-83-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.27 g/mol
Formula C₁₅H₁₃NO₂
badge Registry Numbers
MDL Number MFCD18452378
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Ethyl 9H-carbazole-2-carboxylate finds application in organic synthesis, particularly as a building block for the development of more complex carbazole derivatives. These derivatives are often utilized in the production of organic semiconductors, which are essential components in organic light-emitting diodes (OLEDs) and photovoltaic cells. The compound's ability to form stable, conjugated systems makes it valuable in the design of materials with desirable electronic properties.

Additionally, it is used in the synthesis of pharmaceuticals, where carbazole derivatives exhibit a range of biological activities, including anti-inflammatory, antimicrobial, and anticancer properties. Its role as an intermediate in the preparation of these bioactive molecules highlights its importance in medicinal chemistry.

In material science, the compound contributes to the development of advanced polymers and dyes, where its structural framework enhances the thermal stability and optical properties of the resulting materials. This versatility underscores its significance across various industrial and research applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,510.00
inventory 250mg
10-20 days ฿7,020.00
inventory 1g
10-20 days ฿14,040.00

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ethyl 9H-carbazole-2-carboxylate
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Ethyl 9H-carbazole-2-carboxylate finds application in organic synthesis, particularly as a building block for the development of more complex carbazole derivatives. These derivatives are often utilized in the production of organic semiconductors, which are essential components in organic light-emitting diodes (OLEDs) and photovoltaic cells. The compound's ability to form stable, conjugated systems makes it valuable in the design of materials with desirable electronic properties.

Additionally, it is

Ethyl 9H-carbazole-2-carboxylate finds application in organic synthesis, particularly as a building block for the development of more complex carbazole derivatives. These derivatives are often utilized in the production of organic semiconductors, which are essential components in organic light-emitting diodes (OLEDs) and photovoltaic cells. The compound's ability to form stable, conjugated systems makes it valuable in the design of materials with desirable electronic properties.

Additionally, it is used in the synthesis of pharmaceuticals, where carbazole derivatives exhibit a range of biological activities, including anti-inflammatory, antimicrobial, and anticancer properties. Its role as an intermediate in the preparation of these bioactive molecules highlights its importance in medicinal chemistry.

In material science, the compound contributes to the development of advanced polymers and dyes, where its structural framework enhances the thermal stability and optical properties of the resulting materials. This versatility underscores its significance across various industrial and research applications.

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