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Product Line: Pharmaceutical Chemicals

Spiro[2.2]pent-1-ylamine hydrochloride

CAS 17202-70-9

Molecular structure of Spiro[2.2]pent-1-ylamine hydrochloride

CAS · 17202-70-9

01

Product Overview

Spiro[2.2]pent-1-ylamine hydrochloride is a high-purity pharmaceutical-intermediates supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.

02

Product Specifications

Appearance Light yellow solid
Assay 97% min
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Applications

Spiro[2.2]pent-1-ylamine hydrochloride is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty organic compounds. Its amine functionality allows for reactions such as acylation, alkylation, and reductive amination, enabling the construction of diverse bioactive molecules and heterocyclic frameworks. In drug discovery, it is employed to introduce spirocyclic scaffolds, which can enhance molecular rigidity, receptor selectivity, and metabolic stability of candidate compounds. The compound is also utilized in the development of ligands, catalysts, and other functional materials in research laboratories, where its unique spirocyclic geometry provides structural advantages.

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Benefits

The main benefits of spiro[2.2]pent-1-ylamine hydrochloride include its rigid spirocyclic structure, which imparts conformational stability and can improve binding affinity in drug candidates. The hydrochloride form increases solubility and ease of handling compared to the free amine. Its primary amine group is highly reactive, enabling versatile functionalization and incorporation into complex molecules. The compound is chemically stable under standard laboratory conditions and compatible with a wide range of organic reactions, making it a reliable intermediate for multi-step syntheses.

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Conclusion

Spiro[2.2]pent-1-ylamine hydrochloride is a valuable spirocyclic amine intermediate widely used in pharmaceutical synthesis, agrochemical research, and specialty chemical development. Its rigid spiro structure, reactive amine group, and solubility advantages make it an important building block for creating bioactive molecules and functional materials. As interest in spirocyclic scaffolds continues to grow in medicinal and organic chemistry, this compound remains a critical tool in modern chemical synthesis and drug discovery.

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