AD59143
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 95% | in stock | $19.00 | $13.00 | - + | |
1g | 95% | in stock | $33.00 | $23.00 | - + | |
5g | 95% | in stock | $65.00 | $45.00 | - + | |
10g | 95% | in stock | $102.00 | $71.00 | - + | |
25g | 95% | in stock | $190.00 | $133.00 | - + | |
100g | 95% | in stock | $712.00 | $498.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AD59143 |
Chemical Name: | 5-Chloro-10,11-dihydro-5h-dibenzo[a,d]cycloheptene |
CAS Number: | 1210-33-9 |
Molecular Formula: | C15H13Cl |
Molecular Weight: | 228.7167 |
MDL Number: | MFCD00003592 |
SMILES: | ClC1c2ccccc2CCc2c1cccc2 |
NSC Number: | 86154 |
Complexity: | 214 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 16 |
XLogP3: | 4.3 |
5-Chloro-10,11-dihydro-5H-dibenzo[a,d][7]annulene, commonly referred to as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and reactivity make it valuable for several key applications in organic chemistry. 1. **Cycloaddition Reactions**: $name$ serves as a powerful dienophile in Diels-Alder reactions, facilitating the formation of complex ring systems. Its chlorine substitution enhances regioselectivity and allows for the efficient construction of fused polycyclic structures.2. **Functional Group Transformations**: The chloro group in $name$ can be readily manipulated to introduce various functional groups, enabling the synthesis of diverse derivatives with distinct properties. This versatility makes it a valuable precursor for further derivatization.3. **Aromatic Substitution**: Through electrophilic aromatic substitution reactions, $name$ can undergo selective halogenation, sulfonation, or nitration at specific positions within its aromatic system. This reactivity profile is exploited in the synthesis of pharmaceuticals, agrochemicals, and materials science.4. **Natural Product Synthesis**: $name$ has found utility in the total synthesis of complex natural products due to its ability to form multiple bonds and participate in intricate reaction cascades. Its rigid polycyclic structure mimics key motifs present in biologically active molecules.5. **Materials Chemistry**: The presence of conjugated double bonds in $name$ makes it attractive for applications in materials science, such as organic electronic devices and optoelectronics. Its extended π-system offers opportunities for tuning electronic properties through molecular design.In summary, 5-Chloro-10,11-dihydro-5H-dibenzo[a,d][7]annulene is a valuable tool in chemical synthesis, enabling the construction of elaborate molecular architectures with tailored functionalities. Its diverse reactivity and structural features make it a sought-after compound for advancing synthetic methodology and accessing novel chemical space.