AB54263
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 95% | in stock | $25.00 | $18.00 | - + | |
5g | 95% | in stock | $87.00 | $61.00 | - + | |
25g | 95% | in stock | $118.00 | $83.00 | - + | |
100g | 95% | in stock | $366.00 | $256.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB54263 |
Chemical Name: | 2-Bromopentane |
CAS Number: | 107-81-3 |
Molecular Formula: | C5H11Br |
Molecular Weight: | 151.0448 |
MDL Number: | MFCD00000160 |
SMILES: | CCCC(Br)C |
NSC Number: | 7896 |
Complexity: | 27.1 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 6 |
Rotatable Bond Count: | 2 |
Undefined Atom Stereocenter Count: | 1 |
XLogP3: | 2.7 |
2-Bromopentane, also known as sec-amyl bromide, is a valuable chemical compound commonly used in various chemical synthesis processes. One of the key applications of 2-Bromopentane in chemical synthesis is its role as a versatile alkylating agent. With its bromine functional group attached to a pentane chain, 2-Bromopentane is able to react with nucleophiles to introduce the pentyl group into organic molecules.In organic synthesis, 2-Bromopentane can be utilized for the preparation of higher molecular weight compounds through substitution reactions. For instance, it can undergo a nucleophilic substitution reaction with various nucleophiles such as amines or thiols to form new carbon-carbon or carbon-heteroatom bonds. This enables the introduction of the pentyl group into a wide range of organic molecules, allowing for the synthesis of complex organic compounds.Furthermore, 2-Bromopentane can also serve as a precursor in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its ability to undergo various chemical transformations under mild conditions makes it a valuable building block in the construction of more elaborate organic structures. Overall, 2-Bromopentane plays a crucial role in chemical synthesis by serving as a key intermediate in the preparation of diverse organic compounds.