3-Thiophenemethanol

97%

Reagent Code: #239922
label
Alias 3-thiophene methanol;thiophene-3-methanol
fingerprint
CAS Number 71637-34-8

science Other reagents with same CAS 71637-34-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 114.17 g/mol
Formula C₅H₆OS
badge Registry Numbers
EC Number 275-741-8
MDL Number MFCD00014534
thermostat Physical Properties
Boiling Point 86-88 °C10 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.211 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of thiophene-based active ingredients. It serves as a building block in organic reactions due to the presence of both hydroxyl and thiophene groups, enabling derivatization for functional materials. Commonly employed in the development of conducting polymers, dyes, and sensors. Also utilized in the preparation of ligands for catalysis and in the fabrication of organic semiconductors for electronic devices.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿156.00
inventory 5g
10-20 days ฿850.00
inventory 25g
10-20 days ฿3,500.00
inventory 100g
10-20 days ฿14,000.00

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3-Thiophenemethanol
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of thiophene-based active ingredients. It serves as a building block in organic reactions due to the presence of both hydroxyl and thiophene groups, enabling derivatization for functional materials. Commonly employed in the development of conducting polymers, dyes, and sensors. Also utilized in the preparation of ligands for catalysis and in the fabrication of organic semiconductors for electroni

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of thiophene-based active ingredients. It serves as a building block in organic reactions due to the presence of both hydroxyl and thiophene groups, enabling derivatization for functional materials. Commonly employed in the development of conducting polymers, dyes, and sensors. Also utilized in the preparation of ligands for catalysis and in the fabrication of organic semiconductors for electronic devices.

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