Benzo[d]isoxazole-3-carbaldehyde

97%

Reagent Code: #153561
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CAS Number 84395-93-7

science Other reagents with same CAS 84395-93-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.13 g/mol
Formula C₈H₅NO₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antipsychotic drugs such as risperidone and paliperidone. Its structure serves as a core scaffold in bioactive molecules, enabling the development of compounds with central nervous system activity. Also employed in the preparation of agrochemicals and functional materials due to its reactivity and stability in organic transformations. Commonly utilized in research settings for constructing heterocyclic compounds through condensation, reduction, or cyclization reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿7,180.00
50mg
10-20 days ฿12,720.00
100mg
10-20 days ฿20,230.00
250mg
10-20 days ฿37,990.00
Benzo[d]isoxazole-3-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antipsychotic drugs such as risperidone and paliperidone. Its structure serves as a core scaffold in bioactive molecules, enabling the development of compounds with central nervous system activity. Also employed in the preparation of agrochemicals and functional materials due to its reactivity and stability in organic transformations. Commonly utilized in research settings for constructing heterocyclic compo

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antipsychotic drugs such as risperidone and paliperidone. Its structure serves as a core scaffold in bioactive molecules, enabling the development of compounds with central nervous system activity. Also employed in the preparation of agrochemicals and functional materials due to its reactivity and stability in organic transformations. Commonly utilized in research settings for constructing heterocyclic compounds through condensation, reduction, or cyclization reactions.

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