Bicyclo[4.2.0]octa-1,3,5-trien-7-ol

97%

Reagent Code: #141360
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CAS Number 35447-99-5

science Other reagents with same CAS 35447-99-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 120.14 g/mol
Formula C₈H₈O
badge Registry Numbers
MDL Number MFCD00798161
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as a synthetic intermediate in organic chemistry, this compound plays a key role in the development of complex polycyclic structures. Its strained ring system and hydroxyl functionality make it valuable in cycloaddition reactions and ring-opening transformations. It is often employed in the synthesis of natural products and pharmaceuticals where fused ring systems are required. The reactivity of the alkene groups combined with the alcohol moiety allows for selective modifications, enabling the construction of intricate molecular architectures. Additionally, it serves as a building block in materials science for designing novel organic frameworks with tailored electronic properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,180.00
inventory 1g
10-20 days ฿11,150.00
inventory 5g
10-20 days ฿37,190.00

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Bicyclo[4.2.0]octa-1,3,5-trien-7-ol
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Used primarily as a synthetic intermediate in organic chemistry, this compound plays a key role in the development of complex polycyclic structures. Its strained ring system and hydroxyl functionality make it valuable in cycloaddition reactions and ring-opening transformations. It is often employed in the synthesis of natural products and pharmaceuticals where fused ring systems are required. The reactivity of the alkene groups combined with the alcohol moiety allows for selective modifications, enabling

Used primarily as a synthetic intermediate in organic chemistry, this compound plays a key role in the development of complex polycyclic structures. Its strained ring system and hydroxyl functionality make it valuable in cycloaddition reactions and ring-opening transformations. It is often employed in the synthesis of natural products and pharmaceuticals where fused ring systems are required. The reactivity of the alkene groups combined with the alcohol moiety allows for selective modifications, enabling the construction of intricate molecular architectures. Additionally, it serves as a building block in materials science for designing novel organic frameworks with tailored electronic properties.

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