2-Chloro-3-methylthiophene

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Reagent Code: #158342
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Alias 2-Chloro-3-methylthiophene
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CAS Number 14345-97-2

science Other reagents with same CAS 14345-97-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 132.61 g/mol
Formula C₅H₅ClS
badge Registry Numbers
EC Number 238-296-0
MDL Number MFCD00130083
thermostat Physical Properties
Boiling Point 147-149 °C(lit.)
inventory_2 Storage & Handling
Density 1.211 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antihypertensive drugs and other cardiovascular medications. It is also employed in the development of agrochemicals, including herbicides and insecticides, due to its reactivity and ability to form complex heterocyclic structures. Its methylthiophene backbone makes it valuable in organic electronics and materials science, especially in the design of conductive polymers and organic semiconductors. Additionally, it serves as a building block in the preparation of dyes and functionalized thiophene derivatives used in research and industrial applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿132.00
25g
10-20 days ฿310.00
100g
10-20 days ฿1,190.00
500g
10-20 days ฿5,910.00
2-Chloro-3-methylthiophene
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antihypertensive drugs and other cardiovascular medications. It is also employed in the development of agrochemicals, including herbicides and insecticides, due to its reactivity and ability to form complex heterocyclic structures. Its methylthiophene backbone makes it valuable in organic electronics and materials science, especially in the design of conductive polymers and organic semiconductors. Additional

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antihypertensive drugs and other cardiovascular medications. It is also employed in the development of agrochemicals, including herbicides and insecticides, due to its reactivity and ability to form complex heterocyclic structures. Its methylthiophene backbone makes it valuable in organic electronics and materials science, especially in the design of conductive polymers and organic semiconductors. Additionally, it serves as a building block in the preparation of dyes and functionalized thiophene derivatives used in research and industrial applications.

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