AD75265
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 97% | in stock | $44.00 | $31.00 | - + | |
1g | 97% | in stock | $99.00 | $70.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
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 |
Complexity: | 142 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 1 |
Rotatable Bond Count: | 1 |
XLogP3: | 0.9 |
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.