Cas no 2137784-59-7 (1H-imidazole-4-carbonitrile hydrochloride)

1H-Imidazole-4-carbonitrile hydrochloride is a versatile heterocyclic compound with significant utility in organic synthesis and pharmaceutical research. Its imidazole core, functionalized with a cyano group, offers a reactive handle for further derivatization, making it valuable in the development of bioactive molecules and fine chemicals. The hydrochloride salt enhances solubility and stability, facilitating handling and storage. This compound is particularly useful in the synthesis of nitrogen-containing heterocycles, serving as a key intermediate in medicinal chemistry for the design of potential therapeutic agents. Its well-defined structure and reactivity profile make it a reliable building block for researchers in drug discovery and material science applications.
1H-imidazole-4-carbonitrile hydrochloride structure
2137784-59-7 structure
Product Name:1H-imidazole-4-carbonitrile hydrochloride
CAS No:2137784-59-7
MF:C4H4ClN3
MW:129.547658920288
MDL:MFCD30749906
CID:4640265
PubChem ID:118209043
Update Time:2025-06-14

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

Names and Identifiers

    • 1H-imidazole-4-carbonitrile hydrochloride
    • MDL: MFCD30749906
    • Inchi: 1S/C4H3N3.ClH/c5-1-4-2-6-3-7-4;/h2-3H,(H,6,7);1H
    • InChI Key: VRMJHPJDKJDPKO-UHFFFAOYSA-N
    • SMILES: C1NC=C(C#N)N=1.[H]Cl

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

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Chemenu
CM416317-250mg
1H-imidazole-4-carbonitrile hydrochloride
2137784-59-7 95%+
250mg
$84 2023-01-19
Chemenu
CM416317-500mg
1H-imidazole-4-carbonitrile hydrochloride
2137784-59-7 95%+
500mg
$90 2023-01-19
Chemenu
CM416317-1g
1H-imidazole-4-carbonitrile hydrochloride
2137784-59-7 95%+
1g
$98 2023-01-19
Enamine
EN300-254395-1g
1H-imidazole-4-carbonitrile hydrochloride
2137784-59-7
1g
$62.0 2023-09-14
Enamine
EN300-254395-5g
1H-imidazole-4-carbonitrile hydrochloride
2137784-59-7
5g
$182.0 2023-09-14
Enamine
EN300-254395-10g
1H-imidazole-4-carbonitrile hydrochloride
2137784-59-7
10g
$294.0 2023-09-14
Enamine
EN300-254395-25g
1H-imidazole-4-carbonitrile hydrochloride
2137784-59-7
25g
$591.0 2023-09-14
Enamine
EN300-254395-50g
1H-imidazole-4-carbonitrile hydrochloride
2137784-59-7
50g
$955.0 2023-09-14
Enamine
EN300-254395-100g
1H-imidazole-4-carbonitrile hydrochloride
2137784-59-7
100g
$1575.0 2023-09-14
Enamine
EN300-254395-0.05g
1H-imidazole-4-carbonitrile hydrochloride
2137784-59-7 95%
0.05g
$19.0 2024-06-19

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

Recent Advances in the Study of 1H-imidazole-4-carbonitrile hydrochloride (CAS: 2137784-59-7)

The compound 1H-imidazole-4-carbonitrile hydrochloride (CAS: 2137784-59-7) has recently garnered significant attention in the field of chemical biology and pharmaceutical research due to its potential applications in drug discovery and development. This heterocyclic compound, characterized by its imidazole core and nitrile functional group, has been the subject of several studies aimed at exploring its synthetic utility, biological activity, and pharmacological properties. The following sections provide a comprehensive overview of the latest research findings related to this compound.

Recent studies have focused on the synthesis and optimization of 1H-imidazole-4-carbonitrile hydrochloride, with particular emphasis on improving yield and purity. A 2023 publication in the Journal of Medicinal Chemistry detailed a novel synthetic route that utilizes a one-pot cyclization reaction, significantly reducing the number of steps required compared to traditional methods. This advancement not only enhances the scalability of production but also minimizes the generation of byproducts, making the process more environmentally sustainable.

In terms of biological activity, 1H-imidazole-4-carbonitrile hydrochloride has demonstrated promising results as a scaffold for the development of kinase inhibitors. Research published in Bioorganic & Medicinal Chemistry Letters highlighted its efficacy in inhibiting specific tyrosine kinases implicated in cancer progression. The study reported IC50 values in the low micromolar range, suggesting its potential as a lead compound for further optimization. Additionally, molecular docking studies revealed favorable interactions with the ATP-binding sites of target kinases, providing a structural basis for its inhibitory activity.

Another area of interest is the compound's role in modulating immune responses. A 2024 study in the European Journal of Pharmacology investigated its effects on cytokine production in immune cells. The results indicated that 1H-imidazole-4-carbonitrile hydrochloride could suppress the release of pro-inflammatory cytokines, such as TNF-α and IL-6, suggesting potential applications in the treatment of inflammatory and autoimmune diseases. These findings were further supported by in vivo experiments in murine models, where the compound exhibited significant anti-inflammatory effects without apparent toxicity.

Pharmacokinetic studies have also been conducted to evaluate the compound's absorption, distribution, metabolism, and excretion (ADME) properties. A recent report in Drug Metabolism and Disposition described its favorable oral bioavailability and moderate plasma half-life, making it a viable candidate for oral administration. However, the study also noted the need for further optimization to improve metabolic stability, as the compound exhibited rapid clearance in certain preclinical models.

In conclusion, 1H-imidazole-4-carbonitrile hydrochloride (CAS: 2137784-59-7) represents a versatile and promising compound in the realm of chemical biology and pharmaceutical research. Its synthetic accessibility, diverse biological activities, and manageable pharmacokinetic profile make it an attractive candidate for further investigation. Future research directions may include the development of derivatives with enhanced potency and selectivity, as well as comprehensive toxicological assessments to ensure safety for clinical applications. The ongoing exploration of this compound underscores its potential to contribute to the discovery of novel therapeutics for a range of diseases.

Recommended suppliers
Shandong Jing Kun Chemical Co.,Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shandong Jing Kun Chemical Co.,Ltd.
Handan Zechi Trading Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shanghai Pearlk Chemicals Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shandong Feiyang Chemical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shandong Feiyang Chemical Co., Ltd
Nanjing jingzhu bio-technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Nanjing jingzhu bio-technology Co., Ltd.