Cas no 70591-86-5 (3-(3-Bromophenyl)-3-oxopropanenitrile)

3-(3-Bromophenyl)-3-oxopropanenitrile is a versatile brominated aromatic compound featuring a β-ketonitrile functional group. Its molecular structure combines a phenyl ring substituted with a bromine atom at the meta-position and an active methylene group adjacent to a nitrile, making it a valuable intermediate in organic synthesis. The presence of both electron-withdrawing groups (bromine and nitrile) enhances its reactivity in nucleophilic substitution and condensation reactions. This compound is particularly useful in the preparation of heterocyclic compounds, pharmaceuticals, and agrochemicals. Its high purity and stability ensure consistent performance in synthetic applications, while the bromine substituent offers a handle for further functionalization via cross-coupling reactions.
3-(3-Bromophenyl)-3-oxopropanenitrile structure
70591-86-5 structure
Product Name:3-(3-Bromophenyl)-3-oxopropanenitrile
CAS No:70591-86-5
MF:C9H6BrNO
MW:224.054041385651
MDL:MFCD02260778
CID:562251
PubChem ID:2756839
Update Time:2025-07-02

3-(3-Bromophenyl)-3-oxopropanenitrile Chemical and Physical Properties

Names and Identifiers

    • 3-(3-Bromophenyl)-3-oxopropanenitrile
    • 3-Bromobenzoylacetonitrile
    • Benzenepropanenitrile,3-bromo-b-oxo-
    • VBFNSHGLANEMRM-UHFFFAOYSA-N
    • 3-bromo-beta-oxo-benzenepropanenitrile
    • 2-(3-BROMOBENZOYL)ACETONITRILE
    • 3-(3-bromo-phenyl)-3-oxo-propionitrile
    • 3-(3-Bromo-phenyl)-3-oxo-propionitr
    • PubChem12043
    • KSC498A5H
    • 2-(3-bromobenzoyl)-acetonitrile
    • 3'-BROMOBENZOYLACETONITRILE
    • SBB019256
    • BBL023618
    • STK662213
    • OR7013
    • 11Z-0859
    • SY020617
    • A9305
    • AC-20653
    • CL8855
    • SCHEMBL1786567
    • J-510593
    • DTXSID60373580
    • CS-0094689
    • 70591-86-5
    • AKOS000181729
    • EN300-41330
    • MFCD02260778
    • Z317042126
    • 3-oxo-3-(3-bromophenyl)propionitrile
    • CHEMBL5021965
    • FT-0604207
    • AM83141
    • DB-022374
    • MDL: MFCD02260778
    • Inchi: 1S/C9H6BrNO/c10-8-3-1-2-7(6-8)9(12)4-5-11/h1-3,6H,4H2
    • InChI Key: VBFNSHGLANEMRM-UHFFFAOYSA-N
    • SMILES: BrC1=CC=CC(C(CC#N)=O)=C1

Computed Properties

  • Exact Mass: 222.96300
  • Monoisotopic Mass: 222.963
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 218
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.7
  • Topological Polar Surface Area: 40.9

Experimental Properties

  • Color/Form: No data avaiable
  • Density: 1.1±0.1 g/cm3
  • Melting Point: 93-95°C
  • Boiling Point: 364.8℃ at 760 mmHg
  • Flash Point: 109.6±11.3 °C
  • Refractive Index: 1.574
  • PSA: 40.86000
  • LogP: 2.54548
  • Vapor Pressure: 0.0±0.5 mmHg at 25°C

3-(3-Bromophenyl)-3-oxopropanenitrile Security Information

3-(3-Bromophenyl)-3-oxopropanenitrile Customs Data

  • HS CODE:2926909090
  • Customs Data:

    China Customs Code:

    2926909090

    Overview:

    2926909090 Other nitrile based compounds. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

3-(3-Bromophenyl)-3-oxopropanenitrile Pricemore >>

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3-(3-Bromophenyl)-3-oxopropanenitrile Production Method

Additional information on 3-(3-Bromophenyl)-3-oxopropanenitrile

Recent Advances in the Study of 3-(3-Bromophenyl)-3-oxopropanenitrile (CAS: 70591-86-5)

3-(3-Bromophenyl)-3-oxopropanenitrile (CAS: 70591-86-5) is a chemical compound of significant interest in the field of chemical biology and medicinal chemistry. Recent studies have highlighted its potential as a key intermediate in the synthesis of bioactive molecules and its role in various pharmacological applications. This research brief aims to provide an overview of the latest findings related to this compound, focusing on its synthesis, biological activity, and potential therapeutic applications.

One of the most notable advancements in the study of 3-(3-Bromophenyl)-3-oxopropanenitrile is its application in the synthesis of heterocyclic compounds. A recent study published in the Journal of Medicinal Chemistry demonstrated its utility as a precursor in the construction of pyrazole and pyrimidine derivatives, which are known for their diverse biological activities. The study reported a high-yield synthesis route using 3-(3-Bromophenyl)-3-oxopropanenitrile as the starting material, followed by cyclization reactions to form the desired heterocycles. These derivatives exhibited promising activity against a range of cancer cell lines, suggesting potential applications in oncology.

In addition to its role in heterocyclic synthesis, 3-(3-Bromophenyl)-3-oxopropanenitrile has been investigated for its direct biological effects. A 2023 study in Bioorganic & Medicinal Chemistry Letters explored its inhibitory activity against specific enzymes involved in inflammatory pathways. The compound showed significant inhibition of cyclooxygenase-2 (COX-2), an enzyme implicated in inflammation and pain. This finding opens up possibilities for the development of novel anti-inflammatory agents based on this chemical scaffold.

Further research has delved into the mechanistic aspects of 3-(3-Bromophenyl)-3-oxopropanenitrile's biological activity. A recent paper in Chemical Biology & Drug Design employed molecular docking and dynamics simulations to elucidate the binding interactions of this compound with target proteins. The results indicated strong binding affinities to key residues in the active sites of several disease-related proteins, providing a structural basis for its observed bioactivity. These computational insights are valuable for the rational design of more potent and selective derivatives.

The safety and pharmacokinetic properties of 3-(3-Bromophenyl)-3-oxopropanenitrile have also been a subject of investigation. A preclinical study published in Toxicology Reports assessed the compound's toxicity profile in animal models. The results indicated a favorable safety margin at therapeutic doses, with no significant adverse effects observed. However, further studies are needed to fully characterize its absorption, distribution, metabolism, and excretion (ADME) properties in humans.

In conclusion, recent research on 3-(3-Bromophenyl)-3-oxopropanenitrile (CAS: 70591-86-5) has demonstrated its versatility as a synthetic intermediate and its potential as a bioactive molecule. The compound's ability to serve as a building block for heterocyclic compounds, combined with its direct enzyme inhibitory effects, makes it a promising candidate for further drug development efforts. Future studies should focus on optimizing its pharmacological properties and exploring its therapeutic potential in disease models.

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