5-Methoxyisoindoline hydrochloride

95%

Reagent Code: #209111
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CAS Number 1159822-61-3

science Other reagents with same CAS 1159822-61-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.65 g/mol
Formula C₉H₁₂ClNO
badge Registry Numbers
MDL Number MFCD09997806
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. It plays a role in the production of certain antidepressants and antipsychotic drugs due to its structural similarity to biologically active isoindoline derivatives. Also utilized in research settings for the design of novel compounds with potential neuroprotective or cognitive-enhancing properties. Its methoxy group enhances lipophilicity, aiding in blood-brain barrier penetration, which is beneficial for targeting neurological conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,100.00
inventory 250mg
10-20 days ฿3,300.00
inventory 1g
10-20 days ฿9,050.00
inventory 5g
10-20 days ฿34,150.00

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5-Methoxyisoindoline hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. It plays a role in the production of certain antidepressants and antipsychotic drugs due to its structural similarity to biologically active isoindoline derivatives. Also utilized in research settings for the design of novel compounds with potential neuroprotective or cognitive-enhancing properties. Its methoxy group enhances lipophilicity, aiding in blood-brain barrier

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. It plays a role in the production of certain antidepressants and antipsychotic drugs due to its structural similarity to biologically active isoindoline derivatives. Also utilized in research settings for the design of novel compounds with potential neuroprotective or cognitive-enhancing properties. Its methoxy group enhances lipophilicity, aiding in blood-brain barrier penetration, which is beneficial for targeting neurological conditions.

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