1-Chloro-10H-phenothiazine

97%

Reagent Code: #161865
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CAS Number 1910-85-6

science Other reagents with same CAS 1910-85-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.72 g/mol
Formula C₁₂H₈ClNS
badge Registry Numbers
MDL Number MFCD18447826
thermostat Physical Properties
Boiling Point 392.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed from light

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, especially antipsychotic and antidepressant drugs within the phenothiazine class. It serves as a key building block for modifying the phenothiazine core structure to develop active compounds that interact with dopamine and serotonin receptors in the central nervous system. Its chloro group is highly reactive, enabling further substitution with various side chains to produce agents with tailored neurological effects. Also utilized in research for developing novel bioactive molecules and in the preparation of dyes and photoactive materials due to the stability and electronic properties of the phenothiazine ring system.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,950.00
inventory 250mg
10-20 days ฿2,990.00

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1-Chloro-10H-phenothiazine
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Used primarily as an intermediate in the synthesis of pharmaceuticals, especially antipsychotic and antidepressant drugs within the phenothiazine class. It serves as a key building block for modifying the phenothiazine core structure to develop active compounds that interact with dopamine and serotonin receptors in the central nervous system. Its chloro group is highly reactive, enabling further substitution with various side chains to produce agents with tailored neurological effects. Also utilized in r

Used primarily as an intermediate in the synthesis of pharmaceuticals, especially antipsychotic and antidepressant drugs within the phenothiazine class. It serves as a key building block for modifying the phenothiazine core structure to develop active compounds that interact with dopamine and serotonin receptors in the central nervous system. Its chloro group is highly reactive, enabling further substitution with various side chains to produce agents with tailored neurological effects. Also utilized in research for developing novel bioactive molecules and in the preparation of dyes and photoactive materials due to the stability and electronic properties of the phenothiazine ring system.

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