ETHYL 4H-THIENO[3,2-B]PYRROLE-5-CARBOXYLATE

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Reagent Code: #181857
label
Alias 4H-thiophene[3,2-b]pyrrole-5-carboxylic acid ethyl ester; 4H-thiophene[3,2-B]pyrrole-5-carboxylic acid ethyl ester
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CAS Number 46193-76-4

science Other reagents with same CAS 46193-76-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.24 g/mol
Formula C₉H₉NO₂S
thermostat Physical Properties
Melting Point 131-132°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of conductive polymers, particularly in the production of poly(3,4-ethylenedioxythiophene) (PEDOT) derivatives. Its structure allows for effective π-conjugation, making it valuable in organic electronics such as organic light-emitting diodes (OLEDs), organic photovoltaics, and organic field-effect transistors (OFETs). Also employed in the development of biosensors and electrochromic devices due to its stable electrochemical properties and ease of functionalization. Commonly utilized in research for creating novel organic semiconductors with improved charge transport characteristics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿159.50
inventory 1g
10-20 days ฿810.00
inventory 5g
10-20 days ฿3,610.00
inventory 25g
10-20 days ฿18,050.00
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ETHYL 4H-THIENO[3,2-B]PYRROLE-5-CARBOXYLATE
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Used as a key intermediate in the synthesis of conductive polymers, particularly in the production of poly(3,4-ethylenedioxythiophene) (PEDOT) derivatives. Its structure allows for effective π-conjugation, making it valuable in organic electronics such as organic light-emitting diodes (OLEDs), organic photovoltaics, and organic field-effect transistors (OFETs). Also employed in the development of biosensors and electrochromic devices due to its stable electrochemical properties and ease of functionalizat

Used as a key intermediate in the synthesis of conductive polymers, particularly in the production of poly(3,4-ethylenedioxythiophene) (PEDOT) derivatives. Its structure allows for effective π-conjugation, making it valuable in organic electronics such as organic light-emitting diodes (OLEDs), organic photovoltaics, and organic field-effect transistors (OFETs). Also employed in the development of biosensors and electrochromic devices due to its stable electrochemical properties and ease of functionalization. Commonly utilized in research for creating novel organic semiconductors with improved charge transport characteristics.

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