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AE11269

1048007-93-7 | Masitinib mesylate

Packsize Purity Availability Price Discounted Price    Quantity
5mg 97% in stock $34.00 $24.00 -   +
25mg 97% in stock $62.00 $44.00 -   +
100mg 97% in stock $131.00 $92.00 -   +
250mg 97% in stock $211.00 $148.00 -   +
1g 97% in stock $511.00 $358.00 -   +
5g 97% in stock $1,505.00 $1,054.00 -   +
10g 97% in stock $2,500.00 $1,750.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE11269
Chemical Name: Masitinib mesylate
CAS Number: 1048007-93-7
Molecular Formula: C29H34N6O4S2
Molecular Weight: 594.7481
MDL Number: MFCD12546334
SMILES: CS(=O)(=O)O.CN1CCN(CC1)Cc1ccc(cc1)C(=O)Nc1ccc(c(c1)Nc1scc(n1)c1cccnc1)C

 

Computed Properties
Complexity: 788  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 41  
Hydrogen Bond Acceptor Count: 10  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 7  

 

 

Upstream Synthesis Route
  • Masitinib mesylate is a versatile compound widely used in chemical synthesis for its unique properties and applications. One of the primary applications of Masitinib mesylate in chemical synthesis is as a catalyst in organic reactions. It serves as an efficient catalyst in various transformations, such as Suzuki-Miyaura cross-coupling reactions, Heck reactions, and asymmetric hydrogenation reactions.Furthermore, Masitinib mesylate can also be employed as a reagent in the construction of complex molecular scaffolds due to its ability to facilitate the formation of C-C and C-N bonds. This makes it a valuable tool in the synthesis of pharmaceutical intermediates and natural products.In addition to its catalytic and reagent properties, Masitinib mesylate can act as a chiral ligand in metal-catalyzed reactions, enabling the enantioselective synthesis of various chiral molecules. Its high selectivity and efficiency make it a popular choice for the preparation of optically pure compounds in asymmetric synthesis.Overall, Masitinib mesylate plays a crucial role in advancing the field of chemical synthesis by enabling the efficient and selective formation of complex molecules with diverse applications in pharmaceuticals, agrochemicals, and materials science.
Literature
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