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Home  > Material Science  > Polymer Science  > Polymer Additives  > 1,4,5,6,7,7-Hexachloro-5-norbornene-2,3-dicarboxylic anhydride

AB57392

115-27-5 | 1,4,5,6,7,7-Hexachloro-5-norbornene-2,3-dicarboxylic anhydride

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $16.00 $11.00 -   +
5g 98% in stock $19.00 $13.00 -   +
100g 98% in stock $22.00 $16.00 -   +
500g 98% in stock $69.00 $49.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB57392
Chemical Name: 1,4,5,6,7,7-Hexachloro-5-norbornene-2,3-dicarboxylic anhydride
CAS Number: 115-27-5
Molecular Formula: C9H2Cl6O3
Molecular Weight: 370.8284
MDL Number: MFCD00080438
SMILES: O=C1OC(=O)C2C1C1(Cl)C(=C(C2(C1(Cl)Cl)Cl)Cl)Cl
NSC Number: 22229

 

Computed Properties
Complexity: 498  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 3  
Undefined Atom Stereocenter Count: 4  
XLogP3: 2.4  

 

 

Upstream Synthesis Route
  • 1,4,5,6,7,7-Hexachloro-5-norbornene-2,3-dicarboxylic anhydride, also known as $name$, is a highly versatile compound widely used in chemical synthesis. Its unique structure and reactivity make it a valuable building block in the creation of various organic compounds.One key application of $name$ lies in its utility as a dienophile in Diels-Alder reactions. Due to its electron-withdrawing chlorine atoms, $name$ demonstrates a strong electrophilic nature, making it an excellent candidate for reacting with dienes in cycloaddition reactions. This reactivity allows for the formation of complex and structurally diverse cyclohexene derivatives, which are valuable intermediates in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.Moreover, the presence of multiple chloro substituents in $name$ enhances its potential for further functionalization through nucleophilic substitution reactions. By selectively manipulating these chlorine atoms, chemists can introduce a wide range of functional groups, enabling the tailored design and synthesis of intricate molecular architectures.In summary, the strategic incorporation of 1,4,5,6,7,7-Hexachloro-5-norbornene-2,3-dicarboxylic anhydride into synthetic pathways offers chemists a powerful tool for the construction of complex organic molecules with diverse applications in the fields of medicine, agriculture, and materials science.
Literature
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