(R)-tert-Butyl (6-methoxy-2,3-dihydrobenzofuran-3-yl)carbamate

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Reagent Code: #37296
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CAS Number 2135331-29-0

science Other reagents with same CAS 2135331-29-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.31 g/mol
Formula C₁₄H₁₉NO₄
badge Registry Numbers
MDL Number MFCD31556106
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of chiral molecules. Its structure, featuring a dihydrobenzofuran ring and a tert-butyl carbamate group, makes it valuable for constructing complex molecules with specific stereochemistry. It is often employed in the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of drugs targeting neurological disorders, as the benzofuran moiety is a common pharmacophore in such compounds. Additionally, its chiral nature allows for the creation of enantiomerically pure substances, which are critical in drug development to ensure efficacy and reduce side effects. The methoxy group further enhances its reactivity and selectivity in various chemical transformations, making it a versatile building block in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,539.00
inventory 250mg
10-20 days ฿21,078.00

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(R)-tert-Butyl (6-methoxy-2,3-dihydrobenzofuran-3-yl)carbamate
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This compound is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of chiral molecules. Its structure, featuring a dihydrobenzofuran ring and a tert-butyl carbamate group, makes it valuable for constructing complex molecules with specific stereochemistry. It is often employed in the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of drugs targeting neurological disorders, as the benzofuran moiety is a common pharmacophore in such compounds. Additionally, its chiral nature allows for the creation of enantiomerically pure substances, which are critical in drug development to ensure efficacy and reduce side effects. The methoxy group further enhances its reactivity and selectivity in various chemical transformations, making it a versatile building block in medicinal chemistry.
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