Cas no 2680539-93-7 (4-Cyclohexyl-1H-imidazole hydrochloride)

4-Cyclohexyl-1H-imidazole hydrochloride is a heterocyclic organic compound featuring a cyclohexyl-substituted imidazole core, stabilized as a hydrochloride salt for enhanced handling and solubility. This intermediate is valued for its role in pharmaceutical and agrochemical synthesis, particularly in the development of bioactive molecules. The cyclohexyl group contributes to lipophilicity, influencing binding affinity in target interactions, while the imidazole moiety provides a versatile scaffold for further functionalization. The hydrochloride form ensures improved stability and compatibility in synthetic workflows. Suitable for use in catalysis, ligand design, and medicinal chemistry research, this compound offers a balance of reactivity and structural flexibility for specialized applications.
4-Cyclohexyl-1H-imidazole hydrochloride structure
2680539-93-7 structure
Product Name:4-Cyclohexyl-1H-imidazole hydrochloride
CAS No:2680539-93-7
MF:C9H15ClN2
MW:186.681801080704
MDL:MFCD34183727
CID:5644982
PubChem ID:163321534
Update Time:2025-06-11

4-Cyclohexyl-1H-imidazole hydrochloride Chemical and Physical Properties

Names and Identifiers

    • Z5040180507
    • 2680539-93-7
    • EN300-28257101
    • AT33207
    • 4-CYCLOHEXYL-1H-IMIDAZOLE HYDROCHLORIDE
    • 4-Cyclohexyl-1H-imidazole hydrochloride
    • MDL: MFCD34183727
    • Inchi: 1S/C9H14N2.ClH/c1-2-4-8(5-3-1)9-6-10-7-11-9;/h6-8H,1-5H2,(H,10,11);1H
    • InChI Key: LQCNRSJVQUJPQB-UHFFFAOYSA-N
    • SMILES: Cl.N1C=NC=C1C1CCCCC1

Computed Properties

  • Exact Mass: 186.0923762g/mol
  • Monoisotopic Mass: 186.0923762g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 119
  • 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: 28.7?2

4-Cyclohexyl-1H-imidazole hydrochloride Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Enamine
EN300-28257101-1g
4-cyclohexyl-1H-imidazole hydrochloride
2680539-93-7 95%
1g
$999.0 2023-09-09
Enamine
EN300-28257101-5g
4-cyclohexyl-1H-imidazole hydrochloride
2680539-93-7 95%
5g
$2900.0 2023-09-09
Enamine
EN300-28257101-10g
4-cyclohexyl-1H-imidazole hydrochloride
2680539-93-7 95%
10g
$4299.0 2023-09-09
Enamine
EN300-28257101-0.05g
4-cyclohexyl-1H-imidazole hydrochloride
2680539-93-7 95.0%
0.05g
$232.0 2025-03-19
Enamine
EN300-28257101-0.1g
4-cyclohexyl-1H-imidazole hydrochloride
2680539-93-7 95.0%
0.1g
$347.0 2025-03-19
Enamine
EN300-28257101-0.25g
4-cyclohexyl-1H-imidazole hydrochloride
2680539-93-7 95.0%
0.25g
$494.0 2025-03-19
Enamine
EN300-28257101-0.5g
4-cyclohexyl-1H-imidazole hydrochloride
2680539-93-7 95.0%
0.5g
$780.0 2025-03-19
Enamine
EN300-28257101-1.0g
4-cyclohexyl-1H-imidazole hydrochloride
2680539-93-7 95.0%
1.0g
$999.0 2025-03-19
Enamine
EN300-28257101-2.5g
4-cyclohexyl-1H-imidazole hydrochloride
2680539-93-7 95.0%
2.5g
$1959.0 2025-03-19
Enamine
EN300-28257101-5.0g
4-cyclohexyl-1H-imidazole hydrochloride
2680539-93-7 95.0%
5.0g
$2900.0 2025-03-19

Additional information on 4-Cyclohexyl-1H-imidazole hydrochloride

Introduction to 4-Cyclohexyl-1H-imidazole hydrochloride (CAS No. 2680539-93-7)

4-Cyclohexyl-1H-imidazole hydrochloride, identified by the Chemical Abstracts Service Number (CAS No.) 2680539-93-7, is a significant compound in the realm of pharmaceutical and chemical research. This compound belongs to the imidazole class, which is well-documented for its diverse biological activities and applications in medicinal chemistry. The presence of a cyclohexyl group in its molecular structure introduces unique pharmacokinetic and pharmacodynamic properties, making it a subject of considerable interest in drug development.

The hydrochloride salt form of 4-cyclohexyl-1H-imidazole enhances its solubility in aqueous solutions, a crucial factor for formulation in pharmaceutical applications. This solubility profile is particularly advantageous for developing drug delivery systems that require precise control over bioavailability and therapeutic efficacy. The compound's stability under various conditions further adds to its appeal as a candidate for further investigation.

In recent years, there has been growing interest in imidazole derivatives due to their potential as scaffolds for novel therapeutic agents. The structural motif of imidazole, characterized by a five-membered ring containing two nitrogen atoms, is known to interact favorably with biological targets such as enzymes and receptors. The introduction of the cyclohexyl group in 4-cyclohexyl-1H-imidazole hydrochloride modifies these interactions, potentially leading to new mechanisms of action.

One of the most compelling areas of research involving 4-cyclohexyl-1H-imidazole hydrochloride is its application in the development of antimicrobial agents. The imidazole core has been shown to exhibit activity against a range of pathogens, including bacteria and fungi. Studies have demonstrated that modifications to the imidazole ring can enhance its antimicrobial properties without compromising safety profiles. The cyclohexyl substituent may contribute to improved binding affinity and selectivity, making this compound a promising candidate for further exploration.

Moreover, 4-cyclohexyl-1H-imidazole hydrochloride has shown potential in other therapeutic domains. For instance, researchers have investigated its role in modulating inflammatory responses and immune function. Imidazole derivatives are known to interact with various immunomodulatory pathways, and the structural features of 4-cyclohexyl-1H-imidazole hydrochloride may enable it to influence these pathways selectively. This has implications for the development of treatments for autoimmune diseases and chronic inflammatory conditions.

The synthesis of 4-cyclohexyl-1H-imidazole hydrochloride involves multi-step organic reactions that require careful optimization to ensure high yield and purity. Advanced synthetic methodologies, such as transition metal-catalyzed cross-coupling reactions, have been employed to enhance efficiency and minimize byproduct formation. These synthetic approaches are critical for producing sufficient quantities of the compound for preclinical and clinical studies.

Preclinical studies have provided valuable insights into the pharmacological properties of 4-cyclohexyl-1H-imidazole hydrochloride. These studies have focused on evaluating its efficacy, safety, and pharmacokinetic profile in animal models. Results from these studies suggest that the compound exhibits favorable properties that make it suitable for further development into a therapeutic agent. For example, preliminary data indicate that it may have a broad spectrum of activity against various pathogens while maintaining good tolerability.

The potential applications of 4-cyclohexyl-1H-imidazole hydrochloride extend beyond antimicrobial therapy. Researchers are exploring its utility in the treatment of neurological disorders, where imidazole derivatives have demonstrated neuroprotective effects. The cyclohexyl group may enhance blood-brain barrier penetration, allowing the compound to reach target sites more effectively. This opens up new avenues for treating conditions such as epilepsy and neurodegenerative diseases.

In conclusion, 4-Cyclohexyl-1H-imidazole hydrochloride (CAS No. 2680539-93-7) is a versatile compound with significant potential in pharmaceutical research. Its unique structural features and demonstrated biological activities make it an attractive candidate for developing novel therapeutic agents across multiple disease areas. As research continues to uncover new applications and refine synthetic methodologies, the future prospects for this compound appear promising.

Recommended suppliers
PRIBOLAB PTE.LTD
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
PRIBOLAB PTE.LTD
Yunnanjiuzhen
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Yunnanjiuzhen
Shandong Feiyang Chemical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shandong Feiyang Chemical Co., Ltd
Shandong Jing Kun Chemical Co.,Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shandong Jing Kun Chemical Co.,Ltd.
Changzhou Guanjia Chemical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Changzhou Guanjia Chemical Co., Ltd