AB44335
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | in stock | $23.00 | $16.00 | - + | ||
5g | in stock | $43.00 | $30.00 | - + | ||
25g | in stock | $109.00 | $76.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB44335 |
Chemical Name: | Butadiene monoxide |
CAS Number: | 930-22-3 |
Molecular Formula: | C4H6O |
Molecular Weight: | 70.0898 |
MDL Number: | MFCD00005149 |
SMILES: | C=CC1CO1 |
Complexity: | 49.6 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 5 |
Hydrogen Bond Acceptor Count: | 1 |
Rotatable Bond Count: | 1 |
Undefined Atom Stereocenter Count: | 1 |
XLogP3: | 0.5 |
3,4-Epoxy-1-butene, also known as butadiene monoxide, is a versatile compound widely used in chemical synthesis. This epoxide is particularly valued for its reactivity and ability to undergo various transformation reactions, making it a valuable building block in organic chemistry. In chemical synthesis, 3,4-Epoxy-1-butene serves as a key intermediate for the production of a wide range of compounds.1. Epoxide Opening Reactions: One of the primary applications of 3,4-Epoxy-1-butene in chemical synthesis is its involvement in epoxide opening reactions. By selectively cleaving the epoxide ring, this compound can participate in reactions with nucleophiles such as amines, alcohols, and thiols to yield functionalized products. These reactions are essential in the synthesis of numerous pharmaceuticals, agrochemicals, and fine chemicals.2. Polymerization: 3,4-Epoxy-1-butene can undergo polymerization reactions to form polymeric materials with desirable properties. Through controlled polymerization processes, this compound can be utilized to produce polyesters, polyethers, and other polymers used in a variety of applications, including coatings, adhesives, and plastics.3. Functional Group Transformations: The presence of the epoxide functional group in 3,4-Epoxy-1-butene allows for diverse functional group transformations. By selectively modifying the epoxide moiety, chemists can introduce new functional groups and stereochemistry into organic molecules, enabling the synthesis of complex structures with specific properties and functionalities.Moreover, 3,4-Epoxy-1-butene's unique structure and reactivity make it a valuable tool in the development of novel chemical reactions and synthetic pathways. Its broad utility in chemical synthesis highlights its importance as a versatile building block for the creation of diverse chemical compounds across various industries.
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