Cas no 1051899-49-0 (tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate)

Technical Introduction: tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate is a versatile intermediate in organic synthesis, particularly valued for its dual functionalization with an amine group and a morpholine moiety. The tert-butyloxycarbonyl (Boc) protecting group enhances stability, facilitating handling and storage while allowing selective deprotection for further derivatization. Its structural features make it suitable for constructing pharmacologically active compounds, such as kinase inhibitors or GPCR-targeting molecules. The morpholine ring contributes to improved solubility and pharmacokinetic properties, while the aromatic amine offers a reactive site for coupling or modification. This compound is commonly employed in medicinal chemistry research for scaffold diversification and lead optimization.
tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate structure
1051899-49-0 structure
Product Name:tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate
CAS No:1051899-49-0
MF:C19H30N4O3
MW:362.466504573822
CID:1040190
PubChem ID:69319998
Update Time:2025-09-27

tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate Chemical and Physical Properties

Names and Identifiers

    • tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate
    • tert-butyl 4-(3-amino-5-morpholin-4-ylphenyl)piperazine-1-carboxylate
    • SCHEMBL5122938
    • 1051899-49-0
    • DB-110366
    • tert-Butyl4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate
    • tert-Butyl 4-[3-amino-5-(morpholin-4-yl)phenyl]piperazine-1-carboxylate
    • DTXSID30740240
    • Inchi: 1S/C19H30N4O3/c1-19(2,3)26-18(24)23-6-4-21(5-7-23)16-12-15(20)13-17(14-16)22-8-10-25-11-9-22/h12-14H,4-11,20H2,1-3H3
    • InChI Key: MCVZTEPLNGGOJJ-UHFFFAOYSA-N
    • SMILES: O(C(C)(C)C)C(N1CCN(C2C=C(C=C(C=2)N2CCOCC2)N)CC1)=O

Computed Properties

  • Exact Mass: 362.23179083g/mol
  • Monoisotopic Mass: 362.23179083g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 7
  • Heavy Atom Count: 26
  • Rotatable Bond Count: 5
  • Complexity: 468
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.8
  • Topological Polar Surface Area: 71.3?2

tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Alichem
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tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate
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Chemenu
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Additional information on tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate

Research Brief on tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate (CAS: 1051899-49-0)

In recent years, the compound tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate (CAS: 1051899-49-0) has garnered significant attention in the field of chemical biology and pharmaceutical research. This molecule, characterized by its piperazine and morpholine moieties, has shown promising potential as a key intermediate in the synthesis of bioactive compounds targeting various diseases, including cancer and neurological disorders. The unique structural features of this compound make it a valuable scaffold for drug discovery and development.

Recent studies have focused on the synthesis and optimization of tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate to enhance its pharmacological properties. Researchers have employed advanced synthetic techniques, such as multi-step organic reactions and catalytic methods, to achieve high yields and purity. The compound's ability to interact with specific biological targets, such as kinases and GPCRs, has been explored in vitro and in silico, revealing its potential as a modulator of critical signaling pathways.

One of the most notable applications of this compound is its role in the development of kinase inhibitors. Kinases play a pivotal role in cell proliferation and survival, and their dysregulation is often associated with cancer. Preliminary studies have demonstrated that derivatives of tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate exhibit inhibitory activity against certain oncogenic kinases, suggesting their potential as anticancer agents. Further investigations are underway to evaluate their efficacy and safety in preclinical models.

In addition to its anticancer potential, this compound has also been investigated for its neuroprotective effects. The morpholine and piperazine groups are known to enhance blood-brain barrier permeability, making the compound a candidate for treating neurological disorders such as Alzheimer's and Parkinson's diseases. Recent in vivo studies have shown that the compound can modulate neurotransmitter systems and reduce oxidative stress, highlighting its multifaceted therapeutic potential.

Despite these promising findings, challenges remain in the development of tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate-based therapeutics. Issues such as metabolic stability, bioavailability, and potential off-target effects need to be addressed through further structural optimization and pharmacokinetic studies. Collaborative efforts between academic institutions and pharmaceutical companies are essential to accelerate the translation of these discoveries into clinical applications.

In conclusion, tert-Butyl 4-(3-amino-5-morpholinophenyl)piperazine-1-carboxylate (CAS: 1051899-49-0) represents a versatile and promising scaffold in medicinal chemistry. Its applications in oncology and neurology, coupled with ongoing research efforts, underscore its potential to contribute to the development of next-generation therapeutics. Future studies should focus on elucidating its mechanism of action and optimizing its drug-like properties to fully realize its therapeutic benefits.

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