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628-21-7

Butane, 1,4-diiodo-

Catalog#: AR00IBS9  |   CAS#: 628-21-7  |   MDL#: MFCD00001099  |   MF: C4H8I2  |   MW: 309.9153

Packsize Purity Price Availability Quantity
1g 95% $3.00 Global Stock Buy Now Add To Cart
5g 95% $4.00 Global Stock Buy Now Add To Cart
25g 95% $14.00 Global Stock Buy Now Add To Cart
100g 95% $51.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00IBS9
Chemical Name Butane, 1,4-diiodo-
CAS Number 628-21-7
Molecular Formula C4H8I2
Molecular Weight 309.9153
MDL Number MFCD00001099
SMILES ICCCCI
NSC Number 31721

1,4-Diiodobutane is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. As a dihalogenated organic compound, 1,4-Diiodobutane serves as an important building block in the synthesis of various complex organic molecules. Its four-carbon backbone, functionalized with two iodine atoms at the 1 and 4 positions, enables it to participate in a wide range of chemical reactions.One key application of 1,4-Diiodobutane is in the synthesis of polymers and materials. Its bifunctional nature allows for the formation of cross-linked polymers through reactions with nucleophilic or radical species. This cross-linking capability is essential in the production of materials with specific physical properties, such as elastomers and resins. Additionally, 1,4-Diiodobutane can be utilized as a monomer in the preparation of block copolymers, where its reactivity can be tailored to achieve desired block structures.In organic synthesis, 1,4-Diiodobutane acts as a valuable alkylating agent. The reactivity of the iodine atoms facilitates substitution reactions with a variety of nucleophiles, leading to the introduction of the butyl group into organic molecules. This property makes 1,4-Diiodobutane a useful tool for creating new carbon-carbon bonds and functionalizing organic compounds in a controlled manner.Furthermore, 1,4-Diiodobutane plays a crucial role in the synthesis of pharmaceutical compounds and agrochemicals. By serving as a key intermediate in the preparation of specific molecular scaffolds, it enables the efficient and selective construction of biologically active molecules. Its ability to introduce the butyl group with high regioselectivity and stereoselectivity makes it a valuable reagent in the pharmaceutical industry for the synthesis of drug candidates and lead compounds.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

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