2-Amino-6-(trifluoromethyl)benzoic acid hydrochloride

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Reagent Code: #42721
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CAS Number 918667-28-4

science Other reagents with same CAS 918667-28-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.59 g/mol
Formula C₈H₇ClF₃NO₂
badge Registry Numbers
MDL Number MFCD30729973
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It is particularly valuable in the development of drugs targeting neurological disorders and inflammatory conditions. Its trifluoromethyl group enhances the biological activity and metabolic stability of the resulting compounds. Additionally, it is employed in the preparation of agrochemicals, where it contributes to the creation of herbicides and pesticides with improved efficacy. The compound's unique structure also makes it a useful building block in organic synthesis for creating complex molecules in academic and industrial research settings.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,179.00
inventory 1g
10-20 days ฿2,367.00

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2-Amino-6-(trifluoromethyl)benzoic acid hydrochloride
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Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It is particularly valuable in the development of drugs targeting neurological disorders and inflammatory conditions. Its trifluoromethyl group enhances the biological activity and metabolic stability of the resulting compounds. Additionally, it is employed in the preparation of agrochemicals, where it contributes to the creation of herbicides and pes

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It is particularly valuable in the development of drugs targeting neurological disorders and inflammatory conditions. Its trifluoromethyl group enhances the biological activity and metabolic stability of the resulting compounds. Additionally, it is employed in the preparation of agrochemicals, where it contributes to the creation of herbicides and pesticides with improved efficacy. The compound's unique structure also makes it a useful building block in organic synthesis for creating complex molecules in academic and industrial research settings.

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