3-Thiophenemethylamine

90%

Reagent Code: #242586
label
Alias 3-(aminomethyl)thiophene
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CAS Number 27757-86-4

science Other reagents with same CAS 27757-86-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 113.18 g/mol
Formula C₅H₇NS
badge Registry Numbers
MDL Number MFCD01529872
thermostat Physical Properties
Boiling Point 102°C (15 mmHg)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of certain antipsychotic and antihypertensive drugs. Its structure allows for the development of biologically active molecules due to the presence of both amine and thiophene groups, which are common in medicinal chemistry. Also employed in agrochemicals for the creation of herbicides and fungicides, where the thiophene ring enhances stability and activity. Additionally, it serves as a building block in organic synthesis for creating conductive polymers and other functional materials in electronic applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿800.00
inventory 5g
10-20 days ฿3,500.00
inventory 25g
10-20 days ฿13,000.00

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3-Thiophenemethylamine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of certain antipsychotic and antihypertensive drugs. Its structure allows for the development of biologically active molecules due to the presence of both amine and thiophene groups, which are common in medicinal chemistry. Also employed in agrochemicals for the creation of herbicides and fungicides, where the thiophene ring enhances stability and activity. Additionally, it serves as a building block in organic

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of certain antipsychotic and antihypertensive drugs. Its structure allows for the development of biologically active molecules due to the presence of both amine and thiophene groups, which are common in medicinal chemistry. Also employed in agrochemicals for the creation of herbicides and fungicides, where the thiophene ring enhances stability and activity. Additionally, it serves as a building block in organic synthesis for creating conductive polymers and other functional materials in electronic applications.

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