N,N-Dimethyl-2-(10H-phenothiazin-10-yl)ethanamine hydrochloride

95%

Reagent Code: #214803
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CAS Number 5934-20-3

science Other reagents with same CAS 5934-20-3

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Weight 306.85 g/mol
Formula C₁₆H₁₉ClN₂S
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MDL Number MFCD01706893
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in the synthesis of phenothiazine-based pharmaceuticals, particularly in the development of antipsychotic and antihistaminic drugs. Its structure supports electron transfer properties, making it useful in some organic electronic applications. Also employed in research for photoredox catalysis due to its light-induced redox activity. Shows potential in dye-sensitized solar cells as a donor material because of its stable radical cation formation. Additionally, utilized in analytical chemistry as a derivatizing agent for detecting carbonyl compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,770.00
inventory 250mg
10-20 days ฿6,400.00
inventory 1g
10-20 days ฿17,280.00

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N,N-Dimethyl-2-(10H-phenothiazin-10-yl)ethanamine hydrochloride
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Used as a key intermediate in the synthesis of phenothiazine-based pharmaceuticals, particularly in the development of antipsychotic and antihistaminic drugs. Its structure supports electron transfer properties, making it useful in some organic electronic applications. Also employed in research for photoredox catalysis due to its light-induced redox activity. Shows potential in dye-sensitized solar cells as a donor material because of its stable radical cation formation. Additionally, utilized in analyti

Used as a key intermediate in the synthesis of phenothiazine-based pharmaceuticals, particularly in the development of antipsychotic and antihistaminic drugs. Its structure supports electron transfer properties, making it useful in some organic electronic applications. Also employed in research for photoredox catalysis due to its light-induced redox activity. Shows potential in dye-sensitized solar cells as a donor material because of its stable radical cation formation. Additionally, utilized in analytical chemistry as a derivatizing agent for detecting carbonyl compounds.

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