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56475-44-6

5-iodo-2,2-dimethylpentanenitrile

Catalog#: AR00IARR  |   CAS#: 56475-44-6  |   MDL#: MFCD21132253  |   MF: C7H12IN  |   MW: 237.0814

Packsize Purity Price Availability Quantity
100mg 95% $374.00 1-2 weeks Buy Now Add To Cart
250mg 95% $533.00 1-2 weeks Buy Now Add To Cart
1g 95% $1,064.00 1-2 weeks Buy Now Add To Cart
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Catalog Number AR00IARR
Chemical Name 5-iodo-2,2-dimethylpentanenitrile
CAS Number 56475-44-6
Molecular Formula C7H12IN
Molecular Weight 237.0814
MDL Number MFCD21132253
SMILES ICCCC(C#N)(C)C

5-Iodo-2,2-dimethylpentanenitrile, also known as $name$, is a versatile chemical compound widely used in organic synthesis due to its unique properties and reactivity. This compound serves as a crucial building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. One of the key applications of $name$ in chemical synthesis is as a convenient source of the 5-iodopentyl functional group. This functional group can participate in a variety of synthetic transformations, such as nucleophilic substitution reactions, cross-coupling reactions, and metal-catalyzed reactions. By introducing the 5-iodopentyl moiety into a molecule, chemists can modify its physicochemical properties, enhance its biological activity, or create new chemical entities for further exploration.Moreover, the nitrile group present in $name$ offers additional synthetic opportunities. Nitriles are versatile intermediates that can undergo various transformations, including hydrolysis to carboxylic acids, reduction to primary amines, and conversion to other functional groups like amines or amides. This flexibility makes 5-Iodo-2,2-dimethylpentanenitrile a valuable building block for the synthesis of diverse compounds with potential applications in pharmaceuticals, materials, and fine chemicals industries.In summary, the strategic placement of the iodo and nitrile functional groups in $name$ enables it to play a crucial role in the synthesis of complex molecules with tailor-made properties, making it an indispensable tool for organic chemists in the development of novel chemical entities.
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GHS Pictogram N/A
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