3-Acetyl-6-methoxyindole

95%

Reagent Code: #138713
fingerprint
CAS Number 99532-52-2

science Other reagents with same CAS 99532-52-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.21 g/mol
Formula C₁₁H₁₁NO₂
badge Registry Numbers
MDL Number MFCD08062615
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of serotonin receptor modulators. It serves as a building block in the preparation of bioactive indole derivatives with potential neurological and psychiatric applications. Also employed in research for fluorescent probes due to its indole-based structure, which can be modified to enhance photophysical properties. Its acetyl and methoxy functional groups allow for selective reactions in multi-step organic syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,980.00
inventory 1g
10-20 days ฿5,320.00
inventory 5g
10-20 days ฿21,670.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Acetyl-6-methoxyindole
No image available

Used in the synthesis of pharmaceutical intermediates, particularly in the development of serotonin receptor modulators. It serves as a building block in the preparation of bioactive indole derivatives with potential neurological and psychiatric applications. Also employed in research for fluorescent probes due to its indole-based structure, which can be modified to enhance photophysical properties. Its acetyl and methoxy functional groups allow for selective reactions in multi-step organic syntheses.

Used in the synthesis of pharmaceutical intermediates, particularly in the development of serotonin receptor modulators. It serves as a building block in the preparation of bioactive indole derivatives with potential neurological and psychiatric applications. Also employed in research for fluorescent probes due to its indole-based structure, which can be modified to enhance photophysical properties. Its acetyl and methoxy functional groups allow for selective reactions in multi-step organic syntheses.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...