Sclareol - Moligand™, ≥96% , CAS No.515-03-7

CAS: 515-03-7 Cat. No.: S138935 Peso molecular: 308.50 Beilstein Registry Number: 2054148 Número EC: 208-194-0

GRADE & PURITY Moligand™, ≥96%

Synonyms

1-Naphthalenepropanol, alpha-ethenyldecahydro-2-hydroxy-alpha,2,5,5,8a-pentamethyl-, (alphaR,1R,2R,4aS,8aS)- | 4-06-00-05554 (Beilstein Handbook Reference) | AS-14857 | DTXSID0047111 | CAS-515-03-7 | Sclareol, analytical standard | (1R,2R,8aS)-Decahydro-1

Storage

Room temperature,Cool

Shipped In

Normal

Descripción general

Sclareol, a diterpene compound with a labdane skeleton, is mainly used as a raw material in the fragrance industry. It shows potent cytotoxic and cytostatic effect in human leukemic cell lines.

Application:

Sclareol may be used as a starting material in the synthesis of ambergris fragrance chemicals such as ambraoxide, ambrox, methylambraoxide, ambracetal, ambraketal and epiambraketal. It may also be used in the synthesis of (+)-galanolactone, (-)-8-epi-galanolactone and (+)-labdienedial.

Specifications

Sinónimos

1-Naphthalenepropanol, alpha-ethenyldecahydro-2-hydroxy-alpha, 2, 5, 5, 8a-pentamethyl-, (alphaR, 1R, 2R, 4aS, 8aS)- | 4-06-00-05554 (Beilstein Handbook Reference) | AS-14857 | DTXSID0047111 | CAS-515-03-7 | Sclareol, analytical standard | (1R, 2R, 8aS)-Decahydro-1

Especificaciones y pureza

Moligand™, ≥96%

Condiciones de almacenamiento de almacenamiento

Room temperature, Cool

Enviado en

Normal

Grado

Moligand™

Pureza

≥96%

Nombres e identificadores

• Pubchem Sid: 488188358
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488188358
• Sonrisas canónicas: CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C
• IUPAC Name: (1R,2R,4aS,8aS)-1-[(3R)-3-hydroxy-3-methylpent-4-enyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol
• InChIKey: XVULBTBTFGYVRC-HHUCQEJWSA-N
• INCHI: 1S/C20H36O2/c1-7-18(4,21)13-9-16-19(5)12-8-11-17(2,3)15(19)10-14-20(16,6)22/h7,15-16,21-22H,1,8-14H2,2-6H3/t15-,16+,18-,19-,20+/m0/s1
• Isómeros SMILES: C[C@]12CCCC([C@@H]1CC[C@@]([C@@H]2CC[C@](C)(C=C)O)(C)O)(C)C
• WGK Alemania: 2
• Peso molecular: 308.50
• Beilstein: 2054148

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Prenol lipids
      • Subclass Diterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Prenol lipids
• Subclass: Diterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Diterpenoids
• Alternative Parents: Tertiary alcohols Cyclic alcohols and derivatives Hydrocarbon derivatives
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Diterpenoid - Labdane diterpenoid - Tertiary alcohol - Cyclic alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homopolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.
• External Descriptors: Labdane and halimane diterpenoids

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (humanos)

ACHE Tclin Acetylcholinesterase (18204 Activities)

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RXRG Tclin Retinoid X receptor gamma (646 Activities)

Discover Target: RXRG

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RXRB Tclin Retinoid X receptor beta (726 Activities)

Discover Target: RXRB

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PC-3 (62116 Activities)

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SNU1 (253 Activities)

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A549 (127892 Activities)

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HCT-116 (91556 Activities)

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HUVEC (11049 Activities)

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HeLa (62764 Activities)

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PBMC (10003 Activities)

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Objetivos asociados (no humanos)

Klebsiella pneumoniae (43867 Activities)

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Staphylococcus aureus (210822 Activities)

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Staphylococcus epidermidis (22802 Activities)

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Staphylococcus hominis (482 Activities)

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Escherichia coli (133304 Activities)

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Plasmodium falciparum (966862 Activities)

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Mus musculus (284745 Activities)

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B16 (5829 Activities)

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P388 (20296 Activities)

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RAW264.7 (28094 Activities)

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Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Insoluble in water
• Rotación específica [α]: -4° (C=1,CHCl3)
• Punto de ebullición (°C): 218-220°C/19mmHg
• Punto de fusión (°C): 95-103 °C
• Peso molecular: 308.500 g/mol
• XLogP3: 4.900
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 308.272 Da
• Monoisotopic Mass: 308.272 Da
• Topological Polar Surface Area: 40.500 Ų
• Heavy Atom Count: 22
• Formal Charge: 0
• Complexity: 429.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 5
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Yao Wang, Junhua Qiu, Chengwei Wang, Ruiyu Yang, Fuyou Guo, Tian Li, Shili Li, Lei Yang, Wei Ding.  (2026)  Sustainable Strategy of Natural trans-Anethole in Controlling Bacterial Wilt: Virulence Suppression and Beneficial Microbiome Enrichment.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:41568748] [10.1021/acs.jafc.5c13627]