2-Amino-4-(trifluoromethyl)phenol

98%

Reagent Code: #135611
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CAS Number 454-81-9

science Other reagents with same CAS 454-81-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.12 g/mol
Formula C₇H₆F₃NO
badge Registry Numbers
MDL Number MFCD01731750
thermostat Physical Properties
Melting Point 121-122°C
Boiling Point 234.5°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for antidepressants and antipsychotic drugs. Also employed in the production of agrochemicals, such as herbicides and fungicides, due to its ability to enhance bioactivity and metabolic stability. Its trifluoromethyl group contributes to improved lipophilicity and binding affinity in target molecules. Additionally, it serves as a building block in the preparation of dyes and fluorescent compounds for research and industrial applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,160.00
5g
10-20 days ฿5,390.00
10g
10-20 days ฿10,340.00
25g
10-20 days ฿23,400.00
100g
10-20 days ฿57,040.00
2-Amino-4-(trifluoromethyl)phenol
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for antidepressants and antipsychotic drugs. Also employed in the production of agrochemicals, such as herbicides and fungicides, due to its ability to enhance bioactivity and metabolic stability. Its trifluoromethyl group contributes to improved lipophilicity and binding affinity in target molecules. Additionally, it serves as a building block in the preparation of dyes and fluorescent comp

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for antidepressants and antipsychotic drugs. Also employed in the production of agrochemicals, such as herbicides and fungicides, due to its ability to enhance bioactivity and metabolic stability. Its trifluoromethyl group contributes to improved lipophilicity and binding affinity in target molecules. Additionally, it serves as a building block in the preparation of dyes and fluorescent compounds for research and industrial applications.

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