N-BOC-5-FORMYLISOINDOLINE

98%

Reagent Code: #218713
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CAS Number 253801-15-9

science Other reagents with same CAS 253801-15-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.29 g/mol
Formula C₁₄H₁₇NO₃
thermostat Physical Properties
Melting Point 118-119 °C
Boiling Point 373.5±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.186±0.06 g/cm3(Predicted)
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and bioactive compounds, particularly in the development of kinase inhibitors and other targeted therapies. Its protected aldehyde functionality allows for selective reactions, making it valuable in multi-step organic synthesis. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems. The BOC-protected amine ensures stability during reactions while enabling deprotection when needed. Widely applied in research settings for drug discovery and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,060.00
inventory 250mg
10-20 days ฿6,890.00
inventory 1g
10-20 days ฿22,590.00
N-BOC-5-FORMYLISOINDOLINE
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Used as a key intermediate in the synthesis of pharmaceuticals and bioactive compounds, particularly in the development of kinase inhibitors and other targeted therapies. Its protected aldehyde functionality allows for selective reactions, making it valuable in multi-step organic synthesis. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems. The BOC-protected amine ensures stability during reactions while enabling deprotection when needed. Widely applied in research setti
Used as a key intermediate in the synthesis of pharmaceuticals and bioactive compounds, particularly in the development of kinase inhibitors and other targeted therapies. Its protected aldehyde functionality allows for selective reactions, making it valuable in multi-step organic synthesis. Commonly employed in medicinal chemistry for constructing complex heterocyclic systems. The BOC-protected amine ensures stability during reactions while enabling deprotection when needed. Widely applied in research settings for drug discovery and development.
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