Cas no 130233-83-9 (3-Heptanone,1,7-bis(4-hydroxyphenyl)-)

3-Heptanone,1,7-bis(4-hydroxyphenyl)- is a bisphenol derivative with a central heptanone backbone flanked by two 4-hydroxyphenyl groups. This structure imparts unique chemical properties, including potential reactivity at both the ketone and phenolic functional groups, making it useful in synthetic organic chemistry and polymer applications. Its symmetrical design enhances thermal stability and may contribute to controlled cross-linking in resin formulations. The phenolic hydroxyl groups offer sites for further functionalization, enabling tailored modifications for advanced material development. Suitable for research and industrial applications, this compound serves as a versatile intermediate in the synthesis of high-performance polymers, coatings, or specialty chemicals requiring precise molecular architecture.
3-Heptanone,1,7-bis(4-hydroxyphenyl)- structure
130233-83-9 structure
Product Name:3-Heptanone,1,7-bis(4-hydroxyphenyl)-
CAS No:130233-83-9
MF:C19H22O3
MW:298.376185894012
MDL:MFCD24849364
CID:221034
PubChem ID:14608480
Update Time:2025-11-04

3-Heptanone,1,7-bis(4-hydroxyphenyl)- Chemical and Physical Properties

Names and Identifiers

    • 3-Heptanone,1,7-bis(4-hydroxyphenyl)-
    • Acerogenin G
    • Acetogenin G
    • AKOS040761305
    • Q27139031
    • 130233-83-9
    • UR0
    • 1,7-bis(4-hydroxyphenyl)heptan-3-one
    • CHEMBL1270258
    • BRD-K55160318-001-01-6
    • ACon1_001183
    • CS-0159039
    • CHEBI:70700
    • AcerogeninG
    • MEGxp0_000310
    • HY-N9240
    • 1,7-bis-(4-hydroxyphenyl)-3-heptanone
    • NCGC00169598-01
    • 1,7-bis(4-hydroxyphenyl)-3-heptanone
    • Acerogenin G, >=95% (LC/MS-ELSD)
    • DA-60714
    • MDL： MFCD24849364
    • Inchi： 1S/C19H22O3/c20-17(10-7-16-8-13-19(22)14-9-16)4-2-1-3-15-5-11-18(21)12-6-15/h5-6,8-9,11-14,21-22H,1-4,7,10H2
    • InChI Key： QUHYUSAHBDACNG-UHFFFAOYSA-N
    • SMILES： O=C(CCC1C=CC(=CC=1)O)CCCCC1C=CC(=CC=1)O

Computed Properties

  • Exact Mass: 298.15689456g/mol
  • Monoisotopic Mass: 298.15689456g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 22
  • Rotatable Bond Count: 8
  • Complexity: 313
  • 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: 3.9
  • Topological Polar Surface Area: 57.5?2

Experimental Properties

  • Color/Form: Oil
  • Density: 1.1±0.1 g/cm3
  • Boiling Point: 526.7±40.0 °C at 760 mmHg
  • Flash Point: 286.4±23.8 °C
  • Vapor Pressure: 0.0±1.4 mmHg at 25°C

3-Heptanone,1,7-bis(4-hydroxyphenyl)- Security Information

3-Heptanone,1,7-bis(4-hydroxyphenyl)- Pricemore >>

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3-Heptanone,1,7-bis(4-hydroxyphenyl)- Related Literature

Related Categories

Additional information on 3-Heptanone,1,7-bis(4-hydroxyphenyl)-

Compound Overview: 3-Heptanone, 1,7-Bis(4-Hydroxyphenyl)

3-Heptanone, 1,7-bis(4-hydroxyphenyl), also known by its CAS number CAS No. 130233-83-9, is a complex organic compound with significant potential in various scientific and industrial applications. This compound has garnered attention due to its unique structural properties and functional groups, which make it a valuable subject in contemporary chemical research.

The molecular structure of 3-heptanone is characterized by a seven-carbon chain with ketone functionality at the third position. The presence of two hydroxyl-substituted phenyl groups at the terminal positions (positions 1 and 7) introduces additional complexity and reactivity to the molecule. This combination of functional groups renders the compound highly versatile, enabling it to participate in a wide range of chemical reactions and applications.

Recent studies have highlighted the importance of 1,7-bis(4-hydroxyphenyl) substitution in influencing the compound's physical and chemical properties. Researchers have demonstrated that this substitution pattern enhances the compound's stability under certain conditions while also improving its solubility in polar solvents. These findings are particularly relevant in the context of developing new materials for pharmaceutical and industrial applications.

The synthesis of 3-heptanone, 1,7-bis(4-hydroxyphenyl) involves a multi-step process that typically includes nucleophilic substitution and condensation reactions. Recent advancements in catalytic techniques have enabled more efficient synthesis pathways, reducing production costs and improving yield rates. These developments underscore the compound's growing importance in organic synthesis research.

In terms of applications, 3-heptanone has shown promise in the field of polymer science. Its ability to form stable cross-links with other monomers makes it a potential candidate for developing high-performance polymers with tailored mechanical properties. Additionally, its hydroxyl groups enable it to serve as a versatile building block for constructing more complex molecular architectures.

The latest research findings on this compound have also explored its potential in biochemistry. Studies have shown that 1,7-bis(4-hydroxyphenyl) substitution can influence the compound's interaction with biological systems, making it a potential candidate for drug delivery systems or as a component in bioactive materials.

In conclusion, CAS No. 130233-83-9, or 3-heptanone, 1,7-bis(4-hydroxyphenyl), represents a fascinating area of study within organic chemistry. Its unique structure and functional groups provide ample opportunities for innovation across multiple disciplines. As research continues to uncover new insights into its properties and applications, this compound is poised to play an increasingly important role in both academic and industrial settings.

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