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Home  > Chemistry  > Heterocyclic Building Blocks  > Azetidines  > 3,3-Bis(bromomethyl)-1-(p-toluenesulfonyl)azetidine

AD79419

1041026-61-2 | 3,3-Bis(bromomethyl)-1-(p-toluenesulfonyl)azetidine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $117.00 $82.00 -   +
250mg 95% in stock $156.00 $109.00 -   +
500mg 95% in stock $257.00 $180.00 -   +
1g 95% in stock $386.00 $270.00 -   +
5g 95% in stock $1,300.00 $910.00 -   +
10g 95% in stock $1,997.00 $1,398.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AD79419
Chemical Name: 3,3-Bis(bromomethyl)-1-(p-toluenesulfonyl)azetidine
CAS Number: 1041026-61-2
Molecular Formula: C12H15Br2NO2S
Molecular Weight: 397.126
MDL Number: MFCD18782896
SMILES: BrCC1(CBr)CN(C1)S(=O)(=O)c1ccc(cc1)C

 

Computed Properties
Complexity: 373  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 4  
XLogP3: 2.8  

 

 

Upstream Synthesis Route
  • 3,3-Bis(bromomethyl)-1-tosylazetidine is a versatile reagent widely used in chemical synthesis for its unique reactivity and structural properties. One key application of this compound is in the field of organic synthesis, where it serves as a valuable building block for the preparation of various complex molecules. Due to its functional groups, 3,3-Bis(bromomethyl)-1-tosylazetidine can participate in a range of important chemical reactions such as nucleophilic substitution, elimination, and cross-coupling reactions. This reagent is particularly useful in the formation of carbon-carbon and carbon-heteroatom bonds, making it an essential tool for the construction of organic frameworks with specific functionalities. Additionally, the azetidine ring in this compound imparts rigidity and stereochemical control, enabling precise manipulation of molecular geometry during synthetic transformations. In summary, 3,3-Bis(bromomethyl)-1-tosylazetidine plays a crucial role in enabling the efficient and strategic synthesis of novel compounds with diverse applications in pharmaceuticals, materials science, and agrochemicals.
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