Organotin chemistry remains an active area of ??research in organometallic chemistry, with a wide range of pharmacological, agrochemical, and polymerization applications. Our organotin reagents are used to generate Stille coupling precursors for more complex coupling partners and dehalogenation reactions to provide hydrocarbons later in the synthetic sequence. Organotin reagents are a class of reagents containing organotin compounds, usually referring to reagents used in organic synthesis. Organotin reagents have some unique properties, such as good catalytic activity, selectivity, and mild reaction.

Some common organotin reagents include:

1. Methyltributyltin (Me3SnBu): Methyltributyltin can be used as a deprotection reagent and a hydroxide reagent, and can also be used as a catalyst for electrophilic substitution reactions.

2. Bis(tripropylsilyl)dimethyldiphenyltin ((i-Pr)2SnPh2): commonly used in metal organic chemistry In, such as the Suzuki coupling reaction, can act as a nucleophile.

3. Tetra(tert-butyl)tin (Bu4Sn): widely used as matting catalyst, oxidizing agent, reducing agent and sacrificial ligand.

Organotin reagents usually need to be stored in a dry, cool, and well-ventilated place, and you need to pay attention to safe operation when using them to avoid contact and inhalation of organotin reagents .