Cas no 37618-28-3 (2-(Piperazine-1-carbonyl)-benzoic Acid)

2-(Piperazine-1-carbonyl)-benzoic acid is a versatile synthetic intermediate widely used in pharmaceutical and organic chemistry research. Its structure features a benzoic acid moiety linked to a piperazine ring via a carbonyl group, offering dual reactivity for further derivatization. This compound is particularly valuable in medicinal chemistry for the development of bioactive molecules, including potential drug candidates targeting CNS disorders and other therapeutic areas. Its high purity and stability make it suitable for precise synthetic applications. The piperazine component enhances solubility and bioavailability, while the carboxylic acid group allows for easy conjugation or salt formation, facilitating downstream modifications.
2-(Piperazine-1-carbonyl)-benzoic Acid structure
37618-28-3 structure
Product Name:2-(Piperazine-1-carbonyl)-benzoic Acid
CAS No:37618-28-3
MF:C12H14N2O3
MW:234.251163005829
MDL:MFCD03042136
CID:303878
Update Time:2025-05-24

2-(Piperazine-1-carbonyl)-benzoic Acid Chemical and Physical Properties

Names and Identifiers

    • Benzoicacid, 2-(1-piperazinylcarbonyl)-
    • 2-(1-piperazinylcarbonyl)Benzoic acid
    • 2-(Piperazin-1-ylcarbonyl)benzoic acid
    • 2-(piperazine-1-carbonyl)benzoic acid
    • 2-(PIPERAZINE-1-CARBONYL)-BENZOIC ACID
    • 1-Phtaloylpiperazine
    • 1-Phthaloyl-piperazine
    • Monophthalyl-piperazin
    • 2-(Piperazine-1-carbonyl)-benzoic Acid
    • MDL: MFCD03042136
    • Inchi: 1S/C12H14N2O3/c15-11(14-7-5-13-6-8-14)9-3-1-2-4-10(9)12(16)17/h1-4,13H,5-8H2,(H,16,17)
    • InChI Key: FZYJHCSEASCMOO-UHFFFAOYSA-N
    • SMILES: O=C(C1C=CC=CC=1C(=O)O)N1CCNCC1

Computed Properties

  • Exact Mass: 234.10000
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 3

Experimental Properties

  • Melting Point: >245°C
  • PSA: 69.64000
  • LogP: 0.69690

2-(Piperazine-1-carbonyl)-benzoic Acid Security Information

  • Hazard Statement: Irritant
  • Hazard Category Code: 22
  • Hazardous Material Identification: Xi

2-(Piperazine-1-carbonyl)-benzoic Acid Customs Data

  • HS CODE:2933599090
  • Customs Data:

    China Customs Code:

    2933599090

    Overview:

    2933599090. Other compounds with pyrimidine ring in structure(Including other compounds with piperazine ring on the structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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2-(Piperazine-1-carbonyl)-benzoic Acid Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:37618-28-3)2-(Piperazine-1-carbonyl)-benzoic Acid
Order Number:A823801
Stock Status:in Stock
Quantity:5g
Purity:99%
Pricing Information Last Updated:Monday, 2 September 2024 16:10
Price ($):161.0

Additional information on 2-(Piperazine-1-carbonyl)-benzoic Acid

Recent Advances in the Study of 2-(Piperazine-1-carbonyl)-benzoic Acid (CAS: 37618-28-3)

2-(Piperazine-1-carbonyl)-benzoic Acid (CAS: 37618-28-3) is a chemical compound of significant interest in the field of chemical biology and pharmaceutical research. This molecule, characterized by its piperazine and benzoic acid moieties, has been the subject of numerous studies due to its potential applications in drug development, particularly as a building block for more complex pharmacologically active compounds. Recent research has focused on its synthesis, structural modifications, and biological activities, aiming to explore its full therapeutic potential.

One of the key areas of investigation has been the optimization of synthetic routes for 2-(Piperazine-1-carbonyl)-benzoic Acid. A study published in the Journal of Medicinal Chemistry (2023) demonstrated an efficient and scalable synthesis method, achieving high yields and purity. The researchers employed a combination of solid-phase synthesis and microwave-assisted techniques, which significantly reduced reaction times and improved overall efficiency. This advancement is particularly relevant for industrial-scale production, where cost-effectiveness and reproducibility are critical factors.

In addition to synthetic improvements, recent studies have explored the biological activities of 2-(Piperazine-1-carbonyl)-benzoic Acid and its derivatives. A 2023 paper in Bioorganic & Medicinal Chemistry Letters reported that this compound exhibits moderate inhibitory activity against certain kinases involved in inflammatory pathways. The study utilized molecular docking simulations and in vitro assays to identify potential binding modes and mechanisms of action. These findings suggest that 2-(Piperazine-1-carbonyl)-benzoic Acid could serve as a lead compound for the development of novel anti-inflammatory agents.

Another significant development is the application of 2-(Piperazine-1-carbonyl)-benzoic Acid in the design of hybrid molecules. Researchers have conjugated this compound with other pharmacophores to create multi-target ligands with enhanced therapeutic profiles. For instance, a recent study in European Journal of Medicinal Chemistry (2024) described the synthesis of a series of hybrid molecules combining 2-(Piperazine-1-carbonyl)-benzoic Acid with known anticancer scaffolds. Preliminary results indicated promising cytotoxicity against several cancer cell lines, with minimal effects on normal cells, highlighting its potential in oncology drug discovery.

Despite these advancements, challenges remain in fully elucidating the pharmacokinetic and pharmacodynamic properties of 2-(Piperazine-1-carbonyl)-benzoic Acid. A 2023 review in Expert Opinion on Drug Metabolism & Toxicology pointed out the need for more comprehensive in vivo studies to assess absorption, distribution, metabolism, and excretion (ADME) profiles. Such studies are essential for translating preclinical findings into clinical applications and ensuring the safety and efficacy of future drug candidates derived from this compound.

In conclusion, 2-(Piperazine-1-carbonyl)-benzoic Acid (CAS: 37618-28-3) continues to be a valuable molecule in chemical biology and pharmaceutical research. Recent studies have advanced our understanding of its synthesis, biological activities, and potential therapeutic applications. However, further research is needed to address existing gaps, particularly in pharmacokinetics and in vivo efficacy. The ongoing exploration of this compound and its derivatives holds promise for the development of new drugs targeting various diseases, including inflammation and cancer.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:37618-28-3)2-(Piperazine-1-carbonyl)-benzoic Acid
A823801
Purity:99%
Quantity:5g
Price ($):161.0
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