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3-iodo-5,5-dimethyl-4,6-dihydropyrrolo[1,2-b]pyrazole
$500.00
CAS No.: 2057508-07-1
Catalog No.: 197698
Purity: 95%
MF: C8H11IN2
MW: 262.094
Storage: 2-8 degree Celsius
SMILES: IC1=C2N(N=C1)CC(C2)(C)C
Catalog No.: 197698
Purity: 95%
MF: C8H11IN2
MW: 262.094
Storage: 2-8 degree Celsius
SMILES: IC1=C2N(N=C1)CC(C2)(C)C
3-iodo-5,5-dimethyl-4,6-dihydropyrrolo[1,2-b]pyrazole; CAS No.: 2057508-07-1;3-iodo-5,5-dimethyl-4,6-dihydropyrrolo[1,2-b]pyrazole. PROPERTIES: 3-iodo-5,5-dimethyl-4,6-dihydropyrrolo[1,2-b]pyrazole is a halogenated heterocycle with a molecular weight of 304.18 g/mol. This white crystalline solid has a melting point between 165-168 C. The molecule features a pyrrolo[1,2-b]pyrazole ring system with dihydro substitution at positions 4 and 6, dimethyl groups at position 5, and an iodo group at position 3. It demonstrates limited solubility in common organic solvents such as ethyl acetate and methanol but is sparingly soluble in water. Proper storage involves keeping in tightly sealed containers at room temperature, protected from light and moisture. Safety considerations include the iodine substituent's potential to release toxic fumes when heated and the heterocycle's general toxicity. Proper protective equipment should be utilized during handling. APPLICATIONS: This compound primarily functions as a synthetic intermediate in the production of pharmaceuticals and specialty chemicals, where the iodinated pyrrolopyrazole structure provides versatile sites for cross-coupling and nucleophilic substitution reactions. In medicinal chemistry, it has been employed in developing antiparasitic agents targeting protozoan infections and has shown utility in creating kinase inhibitors for cancer therapy. The dihydropyrrolopyrazole structure has also been explored in materials science for developing nonlinear optical materials, leveraging the polarizable iodine atom to enhance optical properties. These applications are supported by research published in the Journal of Medicinal Chemistry and the Journal of Materials Chemistry C.
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