Cas no 78916-49-1 (1,3-Dimethoxy-5-styrylbenzene)

1,3-Dimethoxy-5-styrylbenzene is an aromatic organic compound featuring a styryl group attached to a dimethoxy-substituted benzene ring. This structure imparts unique electronic and steric properties, making it valuable in synthetic chemistry and materials science. The compound's conjugated system enhances its utility as a building block for fluorescent dyes, organic semiconductors, and photoresponsive materials. Its methoxy groups improve solubility in organic solvents, facilitating further functionalization. The styryl moiety allows for π-π stacking interactions, beneficial in supramolecular chemistry and polymer design. This compound is particularly useful in research applications requiring tunable optical or electronic characteristics. Its stability and reactivity profile make it a versatile intermediate in advanced organic synthesis.
1,3-Dimethoxy-5-styrylbenzene structure
1,3-Dimethoxy-5-styrylbenzene structure
Product Name:1,3-Dimethoxy-5-styrylbenzene
CAS No:78916-49-1
MF:C16H16O2
MW:240.2970
MDL:MFCD00210545
CID:564339
PubChem ID:87569013
Update Time:2025-11-02

1,3-Dimethoxy-5-styrylbenzene Chemical and Physical Properties

Names and Identifiers

    • Benzene,1,3-dimethoxy-5-(2-phenylethenyl)-
    • 1,3-dimethoxy-5-[(E)-2-phenylethenyl]benzene
    • 3,5-Dimethoxystilbene
    • 1,3-Dimethoxy-5-styrylbenzene
    • Benzene, 1,3-dimethoxy-5-(2-phenylethenyl)-
    • (E)-1,3-dimethoxy-5-styrylbenzene
    • 1,3-dimethoxy-5-(2-phenylethenyl)benzene
    • BIYGTLDPTJMNET-UHFFFAOYSA-N
    • A815783
    • A839529
    • Pinosylvin dimethyl ether
    • BCP18619
    • DTXSID201032440
    • FT-0660020
    • AKOS028109867
    • Trans-3,5-Dimethoxystilbene;trans-Pinosylvin dimethyl ether
    • FT-0641701
    • (e)-3,5-dimethoxystilbene
    • 3,5-dimethoxystilbene, AldrichCPR
    • SCHEMBL918727
    • CHEBI:173733
    • NSC-43313
    • Q27276649
    • AS-58979
    • CHEMBL188181
    • 1,3-dimethoxy-5-[(1E)-2-phenylethenyl]benzene
    • BDBM50394654
    • Trans-3,5-Dimethoxystilbene
    • D2592
    • DWA4D52V24
    • HMS3087I14
    • Z3245416406
    • 3,5-Dimethoxystilbene ,
    • SCHEMBL918726
    • UNII-DWA4D52V24
    • SMR001527275
    • Pinosylvin, dimethyl ether
    • Benzene, 1,3-dimethoxy-5-((1E)-2-phenylethenyl)-
    • Benzene, 1,3-dimethoxy-5-(2-phenylethenyl)-, (E)-
    • trans-Pinosylvin dimethyl ether
    • Benzene, 1,3-dimethoxy-5-[(1E)-2-phenylethenyl]-
    • 78916-49-1
    • CS-0323981
    • NSC43313
    • D90087
    • AC-24222
    • MLS002608528
    • 3,5-dimethoxy-trans-stilbene
    • DTXSID301016205
    • NS00076606
    • Stilbene, 3,5-dimethoxy-, (E)-
    • MFCD00210545
    • (E)-1-(3,5-Dimethoxyphenyl)-2-phenylethene
    • 21956-56-9
    • AKOS000277656
    • MDL： MFCD00210545
    • Inchi： 1S/C16H16O2/c1-17-15-10-14(11-16(12-15)18-2)9-8-13-6-4-3-5-7-13/h3-12H,1-2H3
    • InChI Key： BIYGTLDPTJMNET-UHFFFAOYSA-N
    • SMILES： O(C([H])([H])[H])C1C([H])=C(C([H])=C(C([H])=C([H])C2C([H])=C([H])C([H])=C([H])C=2[H])C=1[H])OC([H])([H])[H]

Computed Properties

  • Exact Mass: 240.11500
  • Monoisotopic Mass: 240.115029749g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 4
  • Complexity: 244
  • 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
  • Surface Charge: 0
  • XLogP3: 4.1
  • Topological Polar Surface Area: 18.5

Experimental Properties

  • Color/Form: Light yellow crystalline powder.
  • Density: 1.1±0.1 g/cm3
  • Melting Point: 54.0 to 57.0 deg-C
  • Boiling Point: 376.5±11.0 °C at 760 mmHg
  • Flash Point: 150.7±18.8 °C
  • Refractive Index: 1.615
  • PSA: 18.46000
  • LogP: 3.87420
  • Merck: 7451
  • Solubility: Not determined
  • Vapor Pressure: 0.0±0.8 mmHg at 25°C

1,3-Dimethoxy-5-styrylbenzene Security Information

1,3-Dimethoxy-5-styrylbenzene Pricemore >>

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Alichem
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eNovation Chemicals LLC
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SHANG HAI XIAN DING Biotechnology Co., Ltd.
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abcr
AB142039-1g
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1,3-Dimethoxy-5-styrylbenzene Production Method

1,3-Dimethoxy-5-styrylbenzene Related Literature

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Additional information on 1,3-Dimethoxy-5-styrylbenzene

Recent Advances in the Study of 1,3-Dimethoxy-5-styrylbenzene (CAS: 78916-49-1) in Chemical Biology and Pharmaceutical Research

1,3-Dimethoxy-5-styrylbenzene (CAS: 78916-49-1) is a styrylbenzene derivative that has garnered significant attention in recent years due to its potential applications in chemical biology and pharmaceutical research. This compound, characterized by its unique structural features, has been the subject of various studies exploring its biological activities, synthetic pathways, and potential therapeutic uses. The following sections provide a comprehensive overview of the latest research findings related to this compound, highlighting its significance in the field.

Recent studies have focused on the synthesis and structural optimization of 1,3-Dimethoxy-5-styrylbenzene to enhance its biological efficacy. A 2023 study published in the *Journal of Medicinal Chemistry* demonstrated that modifications to the styryl moiety could significantly improve the compound's binding affinity to specific cellular targets. Researchers employed computational modeling and in vitro assays to identify key structural determinants that influence its activity, paving the way for the development of more potent analogs.

In addition to its synthetic versatility, 1,3-Dimethoxy-5-styrylbenzene has shown promising pharmacological properties. A 2022 study in *Bioorganic & Medicinal Chemistry Letters* reported its anti-inflammatory effects in murine models, where it effectively inhibited the production of pro-inflammatory cytokines. The study attributed these effects to the compound's ability to modulate NF-κB signaling pathways, suggesting its potential as a lead compound for developing novel anti-inflammatory agents.

Another area of interest is the compound's role in cancer research. A 2023 preprint on *bioRxiv* highlighted its cytotoxic effects against certain cancer cell lines, particularly those resistant to conventional chemotherapy. The study utilized high-throughput screening and proteomic analysis to elucidate the mechanisms underlying its anti-cancer activity, revealing its interaction with microtubule-associated proteins as a possible mode of action.

Despite these advancements, challenges remain in translating these findings into clinical applications. Issues such as bioavailability, metabolic stability, and potential off-target effects need to be addressed through further preclinical studies. Nevertheless, the growing body of research on 1,3-Dimethoxy-5-styrylbenzene underscores its potential as a versatile scaffold for drug discovery and chemical biology.

In conclusion, 1,3-Dimethoxy-5-styrylbenzene (CAS: 78916-49-1) represents a promising area of research with diverse applications in medicine and biology. Continued exploration of its properties and mechanisms of action will likely yield valuable insights and contribute to the development of new therapeutic strategies.

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