8-Chloro-benzobnaphtho1,2-dfuran丨CAS 1647008-46-5

8-Chloro-benzobnaphtho1,2-dfuran丨CAS 1647008-46-5
Product Introduction:
Catalog No.: SS118261
CAS No.: 1647008-46-5
Purity: 98% min
Product Name: 8-Chloro-benzobnaphtho1,2-dfuran
Molecular Formula: C16H9ClO
Molecular Weight: 252.7
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Technical Parameters
Description

Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of 8-chloro-benzobnaphtho1,2-dfuran丨cas 1647008-46-5 in China. Welcome to wholesale custom made chemical products at competitive price from our factory. For more cheap products, contact us now.

 

Specifications

 

Appearance: Off-white or white solid
Purity: 98% min

 

 

 

Applications

 

8-Chloro-benzobnaphtho[1,2-d]furan is a polycyclic heteroaromatic compound used primarily as an intermediate in pharmaceutical and organic synthesis. Its fused furan and benzene rings, along with the chloro substituent, make it suitable for the synthesis of bioactive molecules, including antiviral, anticancer, and enzyme inhibitor candidates. The compound is also employed in the development of complex heterocyclic frameworks for medicinal chemistry research and as a building block in the synthesis of specialty organic materials, dyes, and ligands for coordination chemistry.

 

Benefits

 

The compound offers high chemical stability and reactivity due to its fused aromatic system and chloro substituent, enabling selective functionalization through nucleophilic substitution or cross-coupling reactions. Its planar polycyclic structure facilitates the construction of rigid, conjugated frameworks, which are valuable in drug design and material applications. Soluble in common organic solvents and compatible with a range of reaction conditions, it allows reproducible and high-yielding transformations in multi-step syntheses. These properties make it an efficient intermediate for both pharmaceutical and advanced chemical research.

 

Conclusion

 

8-Chloro-benzobnaphtho[1,2-d]furan is a versatile heteroaromatic intermediate useful in pharmaceuticals, material science, and fine chemical synthesis. Its fused ring structure, chloro functionality, and chemical stability support selective derivatization and the preparation of complex bioactive molecules and specialty compounds.

 

 

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