Thiophene-3-acetonitrile

98%

Reagent Code: #241214
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CAS Number 13781-53-8

science Other reagents with same CAS 13781-53-8

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scatter_plot Molecular Information
Weight 123.17 g/mol
Formula C₆H₅NS
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MDL Number MFCD00005471
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and antihypertensive drugs. Its structure allows for easy functionalization, making it valuable in creating active pharmaceutical ingredients (APIs) with heterocyclic frameworks. Also employed in agrochemicals for the production of herbicides and fungicides due to its stability and reactivity. Additionally, it serves in material science for constructing organic semiconductors and conductive polymers, where the thiophene ring enhances electron delocalization.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿1,240.00
inventory 25g
10-20 days ฿2,810.50
inventory 100g
10-20 days ฿16,650.00
Thiophene-3-acetonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and antihypertensive drugs. Its structure allows for easy functionalization, making it valuable in creating active pharmaceutical ingredients (APIs) with heterocyclic frameworks. Also employed in agrochemicals for the production of herbicides and fungicides due to its stability and reactivity. Additionally, it serves in material science for constructing organic semiconductors and conductive pol

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and antihypertensive drugs. Its structure allows for easy functionalization, making it valuable in creating active pharmaceutical ingredients (APIs) with heterocyclic frameworks. Also employed in agrochemicals for the production of herbicides and fungicides due to its stability and reactivity. Additionally, it serves in material science for constructing organic semiconductors and conductive polymers, where the thiophene ring enhances electron delocalization.

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