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Product Line: Pharmaceutical Chemicals

tert-Butyl 4-iodopyrazole-1-carboxylate

CAS 121669-70-3

Molecular structure of tert-Butyl 4-iodopyrazole-1-carboxylate

CAS · 121669-70-3

01

Product Overview

tert-Butyl 4-iodopyrazole-1-carboxylate 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: White to pale yellow solid
Purity(LC): 98% min
Water Content(KF): 0.5% max
03

Applications

tert-Butyl 4-iodopyrazole-1-carboxylate (CAS 121669-70-3) is a valuable heterocyclic intermediate frequently used in pharmaceutical and fine chemical synthesis. It serves as a key building block for the preparation of pyrazole-based drugs, agrochemicals, and biologically active compounds. The iodine substituent at the 4-position allows for diverse cross-coupling reactions such as Suzuki, Sonogashira, or Buchwald–Hartwig coupling, enabling efficient formation of C–C and C–N bonds. This compound is also utilized in medicinal chemistry to construct libraries of heterocyclic molecules with potential anti-inflammatory, antiviral, and anticancer properties.

04

Benefits

The main benefits of tert-Butyl 4-iodopyrazole-1-carboxylate include its high reactivity and synthetic versatility. The tert-butyl carbamate (Boc) protecting group enhances stability and facilitates downstream functionalization under mild conditions. The iodine atom provides excellent leaving group ability, making it an ideal substrate for palladium-catalyzed reactions. Its compatibility with various reaction conditions and ease of purification make it an efficient intermediate for both small-scale research and large-scale industrial applications.

05

Conclusion

tert-Butyl 4-iodopyrazole-1-carboxylate is a highly functionalized reagent that combines stability, reactivity, and adaptability, making it indispensable in modern heterocyclic chemistry. Its role in constructing complex molecular frameworks through cross-coupling reactions underscores its importance in pharmaceutical development and advanced organic synthesis.

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