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AD75265

112892-88-3 | Bicyclo[4.2.0]octa-1,3,5-triene-3-carbaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $44.00 $31.00 -   +
1g 97% in stock $99.00 $70.00 -   +

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*All prices are in USD.

Description
Catalog Number: AD75265
Chemical Name: Bicyclo[4.2.0]octa-1,3,5-triene-3-carbaldehyde
CAS Number: 112892-88-3
Molecular Formula: C9H8O
Molecular Weight: 132.1592
MDL Number: MFCD09752659
SMILES: O=Cc1ccc2c(c1)CC2

 

Computed Properties
Complexity: 142  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 0.9  

 

 

Upstream Synthesis Route
  • Bicyclo[4.2.0]octa-1,3,5-triene-3-carbaldehyde, often referred to simply as $name$, is a versatile chemical compound widely utilized in the field of chemical synthesis. Its unique molecular structure and reactivity make it a valuable building block for the creation of various complex organic molecules.In chemical synthesis, $name$ serves as a key starting material for the preparation of a wide range of carbon-carbon and carbon-heteroatom bond formations. Its conjugated system allows for efficient and selective functionalization reactions, leading to the generation of diverse structural motifs in target molecules. By exploiting the reactivity of the aldehyde group and the proximity of the double bonds in the bicyclic framework, chemists can introduce a variety of substituents and functional groups with precision.Additionally, the strained nature of the bicyclic skeleton in $name$ imparts it with unique reactivity patterns, enabling the synthesis of complex polycyclic structures and natural product analogs. Its role in cascade reactions and domino processes highlights its significance in streamlining synthetic pathways and enhancing overall synthetic efficiency.Overall, the incorporation of Bicyclo[4.2.0]octa-1,3,5-triene-3-carbaldehyde in chemical synthesis facilitates the construction of intricate molecular architectures with strategic control over stereochemistry and functionality, making it a valuable tool for organic chemists striving to access novel compounds and materials.
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