Cas no 408324-00-5 ((3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane)

(3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane is a polyphenolic compound characterized by its stereospecific hydroxylation pattern and extended heptane backbone. Its structural features, including multiple hydroxyl groups on aromatic rings and aliphatic chains, contribute to its potential as an antioxidant and bioactive intermediate. The (3R,5R) configuration ensures stereochemical precision, which may enhance binding affinity in biological systems. This compound is of interest in medicinal chemistry and natural product research due to its structural similarity to curcuminoids and other phenolic metabolites. Its well-defined stereochemistry and polyfunctional nature make it suitable for studies targeting oxidative stress modulation or as a scaffold for derivative synthesis.
(3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane structure
408324-00-5 structure
Product Name:(3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane
CAS No:408324-00-5
MF:C19H24O5
MW:332.390866279602
CID:2000050
PubChem ID:636849
Update Time:2025-10-29

(3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane Chemical and Physical Properties

Names and Identifiers

    • 3,5-Dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane
    • 3,5-Dihydroxy-1-(3,4-dihydroxyphenyl) -7-(4-hydroxyphenyl)heptane
    • (3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane
    • InChI=1/C19H24O5/c20-15-6-1-13(2-7-15)3-8-16(21)12-17(22)9-4-14-5-10-18(23)19(24)11-14/h1-2,5-7,10-11,16-17,20-24H,3-4,8-9,12H2/t16-,17-/m1/s
    • CHEMBL443638
    • 1,2-benzenediol, 4-[(3R,5R)-3,5-dihydroxy-7-(4-hydroxyphenyl)heptyl]-
    • 4-[(3R,5R)-3,5-dihydroxy-7-(4-hydroxyphenyl)heptyl]benzene-1,2-diol
    • 408324-00-5
    • AKOS040761073
    • FS-8831
    • rel-4-[(3R,5R)-3,5-dihydroxy-7-(4-hydroxyphenyl)heptyl]benzene-1,2-diol
    • 4-[3,5-Dihydroxy-7-(4-hydroxy-phenyl)-heptyl]-benzene-1,2-diol
    • CS-0159187
    • Inchi: 1S/C19H24O5/c20-15-6-1-13(2-7-15)3-8-16(21)12-17(22)9-4-14-5-10-18(23)19(24)11-14/h1-2,5-7,10-11,16-17,20-24H,3-4,8-9,12H2/t16-,17-/m1/s1
    • InChI Key: XLTITIJKWVRJMS-IAGOWNOFSA-N
    • SMILES: O[C@H](CCC1C=CC(=C(C=1)O)O)C[C@@H](CCC1C=CC(=CC=1)O)O

Computed Properties

  • Exact Mass: 332.16200
  • Monoisotopic Mass: 332.16237386g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 5
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 24
  • Rotatable Bond Count: 8
  • Complexity: 343
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 2
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.9
  • Topological Polar Surface Area: 101?2

Experimental Properties

  • Color/Form: Oil
  • Density: 1.295±0.06 g/cm3 (20 oC 760 Torr),
  • Boiling Point: 622.1±55.0 °C at 760 mmHg
  • Flash Point: 291.5±26.1 °C
  • Solubility: Very slightly soluble (0.8 g/l) (25 o C),
  • PSA: 101.15000
  • LogP: 2.48070
  • Vapor Pressure: 0.0±1.9 mmHg at 25°C

(3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane Security Information

(3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane Pricemore >>

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Additional information on (3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane

Comprehensive Guide to (3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane (CAS No. 408324-00-5)

(3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane (CAS No. 408324-00-5) is a naturally occurring polyphenolic compound with significant biological and pharmacological potential. This compound, often studied for its antioxidant and anti-inflammatory properties, has garnered attention in recent years due to its potential health benefits. Researchers and industries are increasingly interested in its applications, particularly in nutraceuticals, cosmeceuticals, and functional foods.

The molecular structure of (3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane features multiple hydroxyl groups, which contribute to its strong free radical scavenging activity. This makes it a promising candidate for combating oxidative stress, a key factor in aging and chronic diseases. With the growing consumer demand for natural antioxidants, this compound is being explored as an alternative to synthetic additives in food and cosmetic formulations.

Recent studies have highlighted the potential of CAS No. 408324-00-5 in supporting cardiovascular health and neuroprotection. Its ability to modulate inflammatory pathways has also sparked interest in its use for managing conditions like arthritis and metabolic syndrome. As the global market for plant-derived bioactive compounds expands, this molecule is poised to play a significant role in the development of next-generation health products.

One of the most searched questions related to (3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane is its bioavailability and mechanisms of action. Researchers are investigating ways to enhance its absorption, such as through nanocarrier systems or liposomal encapsulation, to maximize its therapeutic effects. Additionally, its synergy with other polyphenols like resveratrol and curcumin is an area of active exploration.

The compound's presence in traditional medicinal plants has also led to increased interest in ethnopharmacology and herbal medicine research. With consumers leaning toward holistic wellness approaches, CAS No. 408324-00-5 is being studied for its role in traditional healing systems and its potential to bridge the gap between modern science and ancient remedies.

From an industrial perspective, the extraction and purification of (3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane present both challenges and opportunities. Advanced techniques like supercritical fluid extraction and chromatographic purification are being optimized to obtain high-purity batches for research and commercial use. The compound's stability under different processing conditions is another critical area of investigation.

In the cosmetic industry, CAS No. 408324-00-5 is gaining traction as a skin-protective agent due to its ability to neutralize UV-induced damage and promote collagen synthesis. With the rising demand for clean beauty products, this natural compound offers a compelling alternative to synthetic preservatives and stabilizers.

Looking ahead, the future of (3R,5R)-3,5-dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane research lies in uncovering its full therapeutic spectrum and developing efficient delivery systems. As scientific understanding deepens and consumer awareness grows, this compound is likely to become a cornerstone in the development of innovative health and wellness solutions.

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