Tert-butyln-(1,3-dioxaindan-4-yl)carbamate

≥95%

Reagent Code: #244434
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CAS Number 111081-10-8

science Other reagents with same CAS 111081-10-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.25 g/mol
Formula C₁₂H₁₅NO₄
badge Registry Numbers
MDL Number MFCD09038117
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a protected amine intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. The tert-butyl carbamate group provides stability under various reaction conditions while the dioxaindan moiety can act as a masked diol, enabling selective transformations. Commonly employed in multi-step syntheses where chemoselective deprotection is required, especially in the development of bioactive molecules such as protease inhibitors or receptor modulators. Its rigid cyclic structure also aids in conformational control during drug design.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,020.00
inventory 250mg
10-20 days ฿6,980.00
inventory 5g
10-20 days ฿35,330.00
inventory 1g
10-20 days ฿19,420.00
inventory 10g
10-20 days ฿62,490.00
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Tert-butyln-(1,3-dioxaindan-4-yl)carbamate
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Used as a protected amine intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. The tert-butyl carbamate group provides stability under various reaction conditions while the dioxaindan moiety can act as a masked diol, enabling selective transformations. Commonly employed in multi-step syntheses where chemoselective deprotection is required, especially in the development of bioactive molecules such as protease inhibitors or receptor modulators. Its rigid

Used as a protected amine intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. The tert-butyl carbamate group provides stability under various reaction conditions while the dioxaindan moiety can act as a masked diol, enabling selective transformations. Commonly employed in multi-step syntheses where chemoselective deprotection is required, especially in the development of bioactive molecules such as protease inhibitors or receptor modulators. Its rigid cyclic structure also aids in conformational control during drug design.

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