[3-(methylamino)oxetan-3-yl]methanol

97%

Reagent Code: #213266
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CAS Number 1416323-17-5

science Other reagents with same CAS 1416323-17-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 117.148 g/mol
Formula C₅H₁₁NO₂
badge Registry Numbers
MDL Number MFCD22628745
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of complex molecules with enhanced bioavailability and target specificity. Commonly employed in medicinal chemistry for constructing heterocyclic compounds and as a building block in structure-activity relationship (SAR) studies. Also utilized in the preparation of protease inhibitors and kinase inhibitors due to its favorable polarity and hydrogen bonding capacity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿29,850.00
[3-(methylamino)oxetan-3-yl]methanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of complex molecules with enhanced bioavailability and target specificity. Commonly employed in medicinal chemistry for constructing heterocyclic compounds and as a building block in structure-activity relationship (SAR) studies. Also utilized in the preparation of protease inhibitors and kinase inhibitors due to its favorable polarity an

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of complex molecules with enhanced bioavailability and target specificity. Commonly employed in medicinal chemistry for constructing heterocyclic compounds and as a building block in structure-activity relationship (SAR) studies. Also utilized in the preparation of protease inhibitors and kinase inhibitors due to its favorable polarity and hydrogen bonding capacity.

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