O-[[3-(Trifluoromethyl)phenyl]methyl]hydroxylamine hydrochloride

≥95%

Reagent Code: #73414
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CAS Number 15256-07-2

science Other reagents with same CAS 15256-07-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.61 g/mol
Formula C₈H₈F₃NOHCl
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. It is particularly valuable in the development of compounds with trifluoromethyl groups, which enhance biological activity and metabolic stability. The hydroxylamine moiety allows for the introduction of nitrogen-containing functional groups, making it useful in the synthesis of amines, oximes, and other nitrogen derivatives. Its application extends to the production of herbicides, fungicides, and other active ingredients in crop protection. Additionally, it plays a role in medicinal chemistry for the design of drug candidates targeting specific enzymes or receptors. The hydrochloride form ensures better solubility and handling in laboratory and industrial processes.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿2,020.00

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O-[[3-(Trifluoromethyl)phenyl]methyl]hydroxylamine hydrochloride
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Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. It is particularly valuable in the development of compounds with trifluoromethyl groups, which enhance biological activity and metabolic stability. The hydroxylamine moiety allows for the introduction of nitrogen-containing functional groups, making it useful in the synthesis of amines, oximes, and other nitrogen derivatives. Its application extends to the produ

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. It is particularly valuable in the development of compounds with trifluoromethyl groups, which enhance biological activity and metabolic stability. The hydroxylamine moiety allows for the introduction of nitrogen-containing functional groups, making it useful in the synthesis of amines, oximes, and other nitrogen derivatives. Its application extends to the production of herbicides, fungicides, and other active ingredients in crop protection. Additionally, it plays a role in medicinal chemistry for the design of drug candidates targeting specific enzymes or receptors. The hydrochloride form ensures better solubility and handling in laboratory and industrial processes.

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