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Home  > Quetiapine IMpurity P (11-(4-Ethylpiperazin-1-yl)dibenzo[b,f][1,4]thiazepine fuMarate))

AE14509

1011758-03-4 | Quetiapine IMpurity P (11-(4-Ethylpiperazin-1-yl)dibenzo[b,f][1,4]thiazepine fuMarate))

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Description
Catalog Number: AE14509
Chemical Name: Quetiapine IMpurity P (11-(4-Ethylpiperazin-1-yl)dibenzo[b,f][1,4]thiazepine fuMarate))
CAS Number: 1011758-03-4
Molecular Formula: C19H21N3S
Molecular Weight: 323.4551
SMILES: CCN1CCN(CC1)C1=Nc2ccccc2Sc2c1cccc2

 

Upstream Synthesis Route
  • 11-(4-Ethylpiperazin-1-yl)dibenzo[b,f][1,4]thiazepine is a versatile compound widely utilized in chemical synthesis for the development of pharmaceuticals, agrochemicals, and materials. In organic synthesis, this compound acts as a key intermediate in the creation of various bioactive molecules due to its unique structural properties.With its aromatic dibenzo[b,f][1,4]thiazepine core and the functionalized 4-ethylpiperazin-1-yl substituent, 11-(4-Ethylpiperazin-1-yl)dibenzo[b,f][1,4]thiazepine serves as a crucial building block in the preparation of new drug candidates. Its presence imparts desired pharmacological activities to the final compounds, enhancing their efficacy and selectivity.Furthermore, the presence of the piperazine ring in this compound enables it to act as a versatile linker in the construction of molecular scaffolds with enhanced biological properties. This feature makes it a valuable tool in medicinal chemistry for designing targeted therapeutics with improved pharmacokinetic profiles.Overall, the strategic incorporation of 11-(4-Ethylpiperazin-1-yl)dibenzo[b,f][1,4]thiazepine in chemical synthesis offers a pathway to the development of novel compounds with potential applications in drug discovery and material science. Its diverse reactivity and structural characteristics make it a valuable asset in the field of organic chemistry for designing innovative molecules with tailored functions.
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