Cas no 69289-27-6 ((Z)-N'-hydroxybenzenecarboximidamide)

(Z)-N'-hydroxybenzenecarboximidamide is a chemical compound characterized by its imidamide functional group, which exhibits notable reactivity in organic synthesis and coordination chemistry. Its (Z)-configuration confers structural specificity, making it valuable for applications requiring precise stereochemistry. The compound's hydroxyimino moiety enhances its chelating properties, facilitating interactions with metal ions in catalytic or analytical contexts. Additionally, its aromatic benzene ring provides stability while allowing further functionalization. This compound is particularly useful in the synthesis of heterocycles, pharmaceuticals, and ligands for metal complexes. Its balanced reactivity and structural features make it a versatile intermediate in research and industrial processes.
(Z)-N'-hydroxybenzenecarboximidamide structure
69289-27-6 structure
Product Name:(Z)-N'-hydroxybenzenecarboximidamide
CAS No:69289-27-6
MF:C7H8N2O
MW:136.15122127533
CID:4149128
PubChem ID:69186
Update Time:2025-11-02

(Z)-N'-hydroxybenzenecarboximidamide Chemical and Physical Properties

Names and Identifiers

    • Benzenecarboximidamide, N'-hydroxy-, (Z)-
    • Benzenecarboximidamide, N'-hydroxy-, [C(Z)]-
    • (Z)-N'-Hydroxybenzenecarboximidamide
    • 613-92-3
    • (Z)-N'-hydroxybenzamidine
    • benzene, C-amino-C-hydroxyiminomethyl-
    • N-hydroxy-benzenecarboximidamide
    • N-hydroxy benzamidine
    • Enamine_002687
    • MFCD00474011
    • AKOS025243335
    • DTXSID10976787
    • NS00006893
    • N'-Hydroxybenzenecarboximidamide
    • (Z)-N'-hydroxybenzimidamide
    • Benzamidoxime
    • Benzamidoxim
    • 69289-27-6
    • Benzenecarboxamide oxime
    • N-hydroxybenzimidamide
    • Benzamide oxime
    • SY057185
    • N-Hydroxybenzenecarboximidamide;Benzohydroxamamide; (Z)-N'-Hydroxybenzimidamide
    • N-Hydroxy-benzamidine
    • DB-053864
    • N-hydroxybenzene-carboximidamide
    • benzene amidoxime
    • (Z)-N'-hydroxybenzenecarboximidamide
    • Inchi: 1S/C7H8N2O/c8-7(9-10)6-4-2-1-3-5-6/h1-5,10H,(H2,8,9)
    • InChI Key: MXOQNVMDKHLYCZ-UHFFFAOYSA-N
    • SMILES: C(C1C=CC=CC=1)(=N)NO

Computed Properties

  • Exact Mass: 136.063662883Da
  • Monoisotopic Mass: 136.063662883Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 128
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 1
  • XLogP3: 1.1
  • Topological Polar Surface Area: 58.6?2

(Z)-N'-hydroxybenzenecarboximidamide Pricemore >>

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(Z)-N'-hydroxybenzenecarboximidamide Related Literature

Additional information on (Z)-N'-hydroxybenzenecarboximidamide

Comprehensive Guide to (Z)-N'-hydroxybenzenecarboximidamide (CAS No. 69289-27-6): Properties, Applications, and Market Insights

(Z)-N'-hydroxybenzenecarboximidamide (CAS No. 69289-27-6) is a specialized organic compound with significant potential in various scientific and industrial applications. This comprehensive guide explores its chemical properties, synthesis methods, applications, and current market trends. As researchers increasingly focus on hydroxamic acid derivatives and their biological activities, this compound has gained attention in pharmaceutical and biochemical research.

The molecular structure of (Z)-N'-hydroxybenzenecarboximidamide features a hydroxyimino group attached to a benzene ring, making it particularly interesting for studies involving metal chelation and enzyme inhibition. Recent publications have highlighted its potential as a building block for more complex molecules in medicinal chemistry, especially in the development of enzyme inhibitors and antimicrobial agents.

From a synthetic chemistry perspective, (Z)-N'-hydroxybenzenecarboximidamide serves as a valuable intermediate in organic synthesis. Its hydroxylamine functionality allows for diverse chemical transformations, making it useful in creating various heterocyclic compounds. Researchers have utilized this compound in the synthesis of oxadiazoles and triazoles, which are important scaffolds in drug discovery programs.

The compound's chelating properties have drawn interest in materials science applications. Studies suggest potential uses in corrosion inhibition and as a metal ion scavenger in environmental remediation processes. These applications align with current industry trends toward green chemistry solutions and sustainable materials.

In biochemical research, (Z)-N'-hydroxybenzenecarboximidamide has shown promise in studies of enzyme-substrate interactions. Its structural similarity to certain biological intermediates makes it valuable for investigating metabolic pathways. Recent studies have explored its potential as a modulator of enzymatic activity, particularly in systems involving nitrogen metabolism.

The analytical characterization of (Z)-N'-hydroxybenzenecarboximidamide typically involves techniques such as NMR spectroscopy, mass spectrometry, and infrared spectroscopy. These methods confirm the compound's purity and structural integrity, which are crucial for research applications. Standard analytical data for this compound is available in major chemical databases and spectral libraries.

From a commercial perspective, (Z)-N'-hydroxybenzenecarboximidamide (CAS No. 69289-27-6) is available through specialty chemical suppliers catering to the research and development market. Pricing and availability may vary depending on purity requirements and order quantities. The compound is typically supplied as a solid with specified purity levels for laboratory use.

Safety considerations for handling (Z)-N'-hydroxybenzenecarboximidamide follow standard laboratory protocols for organic compounds. While not classified as hazardous under normal conditions, proper personal protective equipment should be used when working with this chemical. Material safety data sheets provide detailed handling and storage recommendations.

Recent patent literature reveals growing interest in derivatives of (Z)-N'-hydroxybenzenecarboximidamide, particularly in pharmaceutical applications. Several patent filings describe its use in creating novel therapeutic agents targeting specific disease pathways. This trend reflects the broader pharmaceutical industry's focus on small molecule drug discovery.

Environmental fate studies of (Z)-N'-hydroxybenzenecarboximidamide indicate moderate biodegradability under standard conditions. Researchers have investigated its environmental persistence and ecotoxicological profile as part of comprehensive green chemistry assessments. These studies contribute to the compound's safety profile for research applications.

The future research potential of (Z)-N'-hydroxybenzenecarboximidamide appears promising, particularly in interdisciplinary applications combining organic synthesis, medicinal chemistry, and materials science. As analytical techniques advance and computational modeling improves, researchers may uncover additional applications for this versatile compound.

For laboratories considering working with (Z)-N'-hydroxybenzenecarboximidamide, it's recommended to consult recent scientific literature for the latest applications and synthetic methodologies. The compound's unique properties continue to make it a valuable tool in various chemical research programs and development projects across multiple disciplines.

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