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Home  > Chemistry  > Heterocyclic Building Blocks  > Other Aromatic Heterocycles  > 5-Chloro-10,11-dihydro-5h-dibenzo[a,d]cycloheptene

AD59143

1210-33-9 | 5-Chloro-10,11-dihydro-5h-dibenzo[a,d]cycloheptene

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.

Description
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

 

Computed Properties
Complexity: 214  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 16  
XLogP3: 4.3  

 

 

Upstream Synthesis Route
  • 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.
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