Dimethylbicyclo[2.1.1]hexane-1,4-dicarboxylate

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Reagent Code: #179711
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CAS Number 42145-38-0

science Other reagents with same CAS 42145-38-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.22 g/mol
Formula C₁₀H₁₄O₄
badge Registry Numbers
MDL Number MFCD22371985
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a specialty building block in organic synthesis, particularly in the development of strained ring systems for pharmaceuticals and advanced materials. Its rigid bicyclic structure makes it valuable in medicinal chemistry for locking molecular conformations, enhancing metabolic stability and target selectivity in drug candidates. It also serves in polymer science to introduce steric constraints that influence the thermal and mechanical properties of resulting polymers. Due to its ester functionality, it can undergo hydrolysis, reduction, or coupling reactions to access a range of derivatives for research and development in agrochemicals and functional molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,400.00

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Dimethylbicyclo[2.1.1]hexane-1,4-dicarboxylate
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Used as a specialty building block in organic synthesis, particularly in the development of strained ring systems for pharmaceuticals and advanced materials. Its rigid bicyclic structure makes it valuable in medicinal chemistry for locking molecular conformations, enhancing metabolic stability and target selectivity in drug candidates. It also serves in polymer science to introduce steric constraints that influence the thermal and mechanical properties of resulting polymers. Due to its ester functionalit

Used as a specialty building block in organic synthesis, particularly in the development of strained ring systems for pharmaceuticals and advanced materials. Its rigid bicyclic structure makes it valuable in medicinal chemistry for locking molecular conformations, enhancing metabolic stability and target selectivity in drug candidates. It also serves in polymer science to introduce steric constraints that influence the thermal and mechanical properties of resulting polymers. Due to its ester functionality, it can undergo hydrolysis, reduction, or coupling reactions to access a range of derivatives for research and development in agrochemicals and functional molecules.

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