2-Thiophenemethanol

97%

Reagent Code: #240372
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CAS Number 636-72-6

science Other reagents with same CAS 636-72-6

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Weight 114.17 g/mol
Formula C₅H₆OS
badge Registry Numbers
MDL Number MFCD00005454
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of certain antihypertensive drugs and fungicides. It serves as a building block in organic reactions due to the reactivity of both the hydroxyl and thiophene groups, enabling the formation of esters, ethers, and other functionalized derivatives. Also employed in the development of conductive polymers and organic semiconductors, where thiophene-based structures contribute to electron delocalization and material stability. Its versatility makes it valuable in research and industrial settings for creating complex molecules with targeted biological or electronic properties.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿470.00
inventory 100g
10-20 days ฿1,870.00
inventory 500g
10-20 days ฿7,610.00

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2-Thiophenemethanol
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of certain antihypertensive drugs and fungicides. It serves as a building block in organic reactions due to the reactivity of both the hydroxyl and thiophene groups, enabling the formation of esters, ethers, and other functionalized derivatives. Also employed in the development of conductive polymers and organic semiconductors, where thiophene-based structures contribute to electron delocalizatio

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of certain antihypertensive drugs and fungicides. It serves as a building block in organic reactions due to the reactivity of both the hydroxyl and thiophene groups, enabling the formation of esters, ethers, and other functionalized derivatives. Also employed in the development of conductive polymers and organic semiconductors, where thiophene-based structures contribute to electron delocalization and material stability. Its versatility makes it valuable in research and industrial settings for creating complex molecules with targeted biological or electronic properties.

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