2-(1-Cycloocten-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #160598
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CAS Number 448211-45-8

science Other reagents with same CAS 448211-45-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.16 g/mol
Formula C₁₄H₂₅BO₂
badge Registry Numbers
MDL Number MFCD16659019
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a reagent in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions. It serves as a boron-based coupling partner to introduce cyclooctenyl groups into aromatic or heteroaromatic systems, enabling the construction of complex organic molecules. Its stability and reactivity make it valuable in pharmaceutical research and development of functional materials. Commonly employed in late-stage functionalization due to the strained cyclooctene ring, which can undergo further transformations such as ring-opening or cycloaddition reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿2,070.00
100mg
10-20 days ฿4,980.00
2-(1-Cycloocten-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used primarily as a reagent in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions. It serves as a boron-based coupling partner to introduce cyclooctenyl groups into aromatic or heteroaromatic systems, enabling the construction of complex organic molecules. Its stability and reactivity make it valuable in pharmaceutical research and development of functional materials. Commonly employed in late-stage functionalization due to the strained cyclooctene ring, which can undergo further tr

Used primarily as a reagent in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions. It serves as a boron-based coupling partner to introduce cyclooctenyl groups into aromatic or heteroaromatic systems, enabling the construction of complex organic molecules. Its stability and reactivity make it valuable in pharmaceutical research and development of functional materials. Commonly employed in late-stage functionalization due to the strained cyclooctene ring, which can undergo further transformations such as ring-opening or cycloaddition reactions.

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