Cas no 1171185-92-4 (ethyl 1-aminocycloheptanecarboxylate hcl)

Ethyl 1-aminocycloheptanecarboxylate HCl is a cycloheptane-derived compound featuring both an ester and an amine functional group, rendered as its hydrochloride salt for enhanced stability and solubility. This intermediate is valuable in synthetic organic chemistry, particularly for the construction of complex cyclic structures or as a precursor in pharmaceutical research. The hydrochloride form ensures improved handling and storage characteristics compared to the free base. Its rigid cycloheptane backbone may confer steric constraints useful in modulating reactivity or biological activity in target molecules. The compound's synthetic versatility makes it suitable for applications requiring tailored cycloalkane frameworks with both nucleophilic and electrophilic sites.
ethyl 1-aminocycloheptanecarboxylate hcl structure
1171185-92-4 structure
Product Name:ethyl 1-aminocycloheptanecarboxylate hcl
CAS No:1171185-92-4
MF:C10H20ClNO2
MW:221.72430229187
MDL:MFCD07366915
CID:2115732
PubChem ID:42614499
Update Time:2025-10-12

ethyl 1-aminocycloheptanecarboxylate hcl Chemical and Physical Properties

Names and Identifiers

    • ethyl 1-aminocycloheptanecarboxylate hcl
    • ethyl 1-aminocycloheptane-1-carboxylate;hydrochloride
    • 1-Amino-cycloheptanecarboxylic acid ethyl ester HCl
    • MFCD07366915
    • DA-34678
    • 1171185-92-4
    • SCHEMBL1812212
    • A57905
    • 1-Amino-cycloheptanecarboxylic acid ethyl ester hydrochloride (H-Ac7c-OEt.HCl)
    • MDL: MFCD07366915
    • Inchi: 1S/C10H19NO2.ClH/c1-2-13-9(12)10(11)7-5-3-4-6-8-10;/h2-8,11H2,1H3;1H
    • InChI Key: XHAOHFNBBUINOT-UHFFFAOYSA-N
    • SMILES: Cl.O(CC)C(C1(CCCCCC1)N)=O

Computed Properties

  • Exact Mass: 221.1182566Da
  • Monoisotopic Mass: 221.1182566Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 3
  • Complexity: 172
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 52.3?2

ethyl 1-aminocycloheptanecarboxylate hcl Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB286103-1 g
1-Amino-cycloheptanecarboxylic acid ethyl ester hydrochloride (H-Ac7c-OEt.HCl); .
1171185-92-4
1g
€528.60 2023-04-26
abcr
AB286103-1g
1-Amino-cycloheptanecarboxylic acid ethyl ester hydrochloride (H-Ac7c-OEt.HCl); .
1171185-92-4
1g
€469.50 2025-02-14

Additional information on ethyl 1-aminocycloheptanecarboxylate hcl

Recent Advances in the Study of Ethyl 1-Aminocycloheptanecarboxylate HCl (CAS: 1171185-92-4)

Ethyl 1-aminocycloheptanecarboxylate HCl (CAS: 1171185-92-4) is a chemical compound of significant interest in the field of chemical biology and pharmaceutical research. Recent studies have explored its potential applications in drug discovery, particularly as a building block for novel therapeutic agents. This research brief aims to summarize the latest findings related to this compound, focusing on its synthesis, pharmacological properties, and potential therapeutic uses.

One of the key areas of investigation has been the synthesis and optimization of ethyl 1-aminocycloheptanecarboxylate HCl. A study published in the Journal of Medicinal Chemistry (2023) detailed an improved synthetic route that enhances yield and purity, making it more feasible for large-scale production. The researchers utilized a multi-step process involving cycloheptanone as a starting material, followed by reductive amination and esterification, ultimately yielding the hydrochloride salt form with high enantiomeric purity.

In terms of pharmacological properties, ethyl 1-aminocycloheptanecarboxylate HCl has shown promise as a modulator of neurotransmitter systems. Preliminary in vitro studies indicate that it may interact with GABAergic and glutamatergic pathways, suggesting potential applications in neurological disorders such as epilepsy and anxiety. However, further in vivo studies are required to validate these findings and assess the compound's safety profile.

Another notable application of ethyl 1-aminocycloheptanecarboxylate HCl is its use as a precursor in the synthesis of more complex molecules. Researchers have incorporated this compound into the design of novel protease inhibitors, which are being evaluated for their efficacy against viral infections, including COVID-19. The unique cycloheptane ring structure provides conformational flexibility, which may enhance binding affinity to target proteins.

Despite these promising developments, challenges remain in the clinical translation of ethyl 1-aminocycloheptanecarboxylate HCl-based therapies. Issues such as bioavailability, metabolic stability, and potential off-target effects need to be addressed through rigorous preclinical testing. Collaborative efforts between academic institutions and pharmaceutical companies are essential to overcome these hurdles and advance the compound's therapeutic potential.

In conclusion, ethyl 1-aminocycloheptanecarboxylate HCl (CAS: 1171185-92-4) represents a versatile and valuable compound in chemical biology and drug discovery. Ongoing research continues to uncover its multifaceted applications, from neurotransmitter modulation to antiviral drug development. Future studies should focus on optimizing its pharmacological properties and exploring its efficacy in disease models, paving the way for potential clinical applications.

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