Asarone - ≥99% , CAS No.2883-98-9

CAS: 2883-98-9 Cat. No.: A101552 Fórmula: C₁₂H₁₆O₃ Peso molecular: 208.25 Beilstein Registry Number: 1910606 Número EC: 220-743-6

CALIDAD & PUREZA ≥99%

Synonyms

2,5-Trimethoxy-1-propenylbenzene|Asaron|1,2,4-Trimethoxy-5-[(1E)-1-propenyl]benzene|alpha -Asarone|ZE-Asarone|(E)-1,2,4-TRIMETHOXY-5-(PROP-1-EN-1-YL)BENZENE|ASARONE [WHO-DD]|Isoasaron (6CI)|Benzene,2,4-trimethoxy-5-(1-propenyl)-|Alpha-asarone alpha-asarone|(E)-2,4,5-Trimethoxypropenylbenzene|Isoasaron|1,2,4-trimethoxy-5-trans-propenyl-benzene|(E)-1,2,4-trimethoxy-5-(prop-1-enyl)benzene|Benzene, 1,2,4-trimethoxy-5-(1E)-1-propenyl-|1,2,4-trimethoxy-5-[(E)-prop-1-enyl]benzene|1,2,4-Trimethoxy-5-(1E)-1-propen-1-ylbenzene|TRANS-ASARONE|1,2,4-Trimethoxy-5-(1-propenyl)-(E)-Benzene|alpha-Asaron|Azaron|benzene, 1,2,4-trimethoxy-5-(1E)-1-propen-1-yl-|.ALPHA.-ASARON|Benzene, 1,2,4-trimethoxy-5-propenyl-, (E)-|Trans-(alpha )-asarone|A-ASARONE|1,2,4-Trimethoxy-5-(1-propenyl)benzene|.ALPHA.-ASARONE|1,2,4-Trimethoxy-5-propenylbenzene|1,2,4-trimethoxy-5-propenyl-benzene|1,2,4-Trimethoxy-5-propenyl-trans-Benzene|Benzene, 1,2,4-trimethoxy-5-propenyl-|trans-1,2,4-Trimethoxy-5-(1-propenyl)benzene|Alpha-Asarone ,(S)|Benzene, 1,2,4-trimethoxy-5-propenyl-, trans-|Benzene, 1,2,4-trimethoxy-5-(1-propenyl)-|Asarabacca camphor|Asarone|ASARONE [HSDB]|benzene, 1,2,4-trimethoxy-5-[(1E)-1-propenyl]-|Etherophenol|1,2,4-trimethoxy-5-[(1E)-prop-1-en-1-yl]benzene|1,2,4-Trimethoxy-5-propenyl-(E)-Benzene|(E)-Asarone|2,4,5-Trimethoxy-1-propenylbenzene|(E)-1,2,4-Trimethoxy-5-(1-propenyl)benzene|alpha-Asarone|trans-2,4,5-Trimethoxypropenylbenzene|trans-Isoasaron|ASARONE;2,4,5-TRIMETHOXY-1-PROPENYLBENZENE|Benzene, 1,2,4-trimethoxy-5-(1-propenyl)-, (E)-|trans-Isoasarone|1,2,4-trimethoxy-5-(prop-1-en-1-yl)benzene|Benzene,2,4-trimethoxy-5-propenyl-|ASARONE, ALPHA-|trans-1,2,4-Trimethoxy-5-(1-propenyl)benzene trans-1-Propenyl-2,4,5-trimethoxybenzene

Storage

Room temperature

Shipped In

Normal

Especificaciones

Sinónimos

2,5-Trimethoxy-1-propenylbenzene | Asaron | 1,2,4-Trimethoxy-5-[(1E)-1-propenyl]benzene | alpha -Asarone | ZE-Asarone | (E)-1,2,4-TRIMETHOXY-5-(PROP-1-EN-1-YL)BENZENE | ASARONE [WHO-DD] | Isoasaron (6CI) | Benzene,2,4-trimethoxy-5-(1-propenyl)- | Alpha-asarone alpha-asarone | (E)-2,4,5-Trimethoxypropenylbenzene | Isoasaron | 1,2,4-trimeth Show more

Especificaciones y pureza

≥99%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥99%

Nombres e identificadores

Pubchem Sid

488190840

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488190840

Sonrisas canónicas

CC=CC1=CC(=C(C=C1OC)OC)OC

IUPAC Name

1,2,4-trimethoxy-5-[(E)-prop-1-enyl]benzene

InChIKey

RKFAZBXYICVSKP-AATRIKPKSA-N

INCHI

1S/C12H16O3/c1-5-6-9-7-11(14-3)12(15-4)8-10(9)13-2/h5-8H,1-4H3/b6-5+

Isómeros SMILES

C/C=C/C1=CC(=C(C=C1OC)OC)OC

WGK Alemania

3

RTECS

DC2975000

Peso molecular

208.25

Beilstein

1910606

Reaxy-Rn

2210026

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2210026&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Phenol ethers
      • Subclass Anisoles

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Phenol ethers
• Subclass: Anisoles
• Intermediate Tree Nodes: Not available
• Direct Parent: Anisoles
• Alternative Parents: Styrenes Phenoxy compounds Methoxybenzenes Alkyl aryl ethers Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenoxy compound - Methoxybenzene - Styrene - Anisole - Alkyl aryl ether - Monocyclic benzene moiety - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof.
• External Descriptors: asarone

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)

HMGCR Tclin 3-hydroxy-3-methylglutaryl-coenzyme A reductase (1 Activities)

Discover Target: HMGCR

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

HMGCR Tclin HMG-CoA reductase (2475 Activities)

Discover Target: HMGCR

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CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)

Discover Target: CYP2D6

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CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

Discover Target: CYP3A4

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Homo sapiens (32628 Activities)

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Objetivos asociados (no humanos)

Hdac6 Histone deacetylase 6 (222 Activities)

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Pseudomonas aeruginosa (123386 Activities)

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Burkholderia cepacia (649 Activities)

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Enterobacter cloacae (7976 Activities)

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Klebsiella pneumoniae (43867 Activities)

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Micrococcus luteus (7463 Activities)

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Staphylococcus aureus (210822 Activities)

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Staphylococcus epidermidis (22802 Activities)

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Escherichia coli (133304 Activities)

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Aspergillus flavus (8875 Activities)

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Aspergillus niger (16508 Activities)

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Bacillus subtilis (32866 Activities)

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Saccharomyces cerevisiae (19171 Activities)

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Cutibacterium acnes (887 Activities)

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Pichia kudriavzevii (7448 Activities)

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Candida albicans (78123 Activities)

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Candida parapsilosis (8521 Activities)

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Fusarium oxysporum (3998 Activities)

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Trichophyton rubrum (3646 Activities)

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Manduca sexta (30 Activities)

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Caenorhabditis elegans (1055 Activities)

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Aedes aegypti (630 Activities)

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Mus musculus (284745 Activities)

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Rattus norvegicus (775804 Activities)

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Heliothis virescens (272 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Aspergillus parasiticus (296 Activities)

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Bursaphelenchus xylophilus (372 Activities)

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Helicoverpa zea (137 Activities)

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Malassezia furfur (70 Activities)

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Panagrellus redivivus (38 Activities)

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HMGCR 3-hydroxy-3-methylglutaryl-coenzyme A reductase (17 Activities)

Discover Target: HMGCR

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Aspergillus sydowii (55 Activities)

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Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Insoluble in water; Degree of Solubility in water: 102 mg/l 25 °C; Soluble in Alcohol,Ether
• Sensibilidad: Light Sensitive
• Punto de ebullición (°C): 296°C
• Punto de fusión (°C): 57-61°C
• Peso molecular: 208.250 g/mol
• XLogP3: 3.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 208.11 Da
• Monoisotopic Mass: 208.11 Da
• Topological Polar Surface Area: 27.700 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 203.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 1
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1

Preguntas frecuentes

What is the purity of this product?

This product is supplied at ≥99% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at room temperature.

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 2883-98-9, the molecular formula is C12H16O3, and the molecular weight is 208.25 g/mol. InChIKey RKFAZBXYICVSKP-AATRIKPKSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.