Asarone - ≥98% , CAS No.2883-98-9

CAS: 2883-98-9 Cat. No.: A299024 Formule: C₁₂H₁₆O₃ Poids moléculaire: 208.25 Beilstein Registry Number: 1910606 Numéro CE: 220-743-6

QUALITÉ & PURETÉ ≥98%

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

Spécifications

Synonymes

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 Afficher plus

Spécifications et pureté

≥98%

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Type d'action

ACTIVATOR

Pureté

≥98%

Noms et identifiants

Sourires canoniques

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+

Isomères SMILES

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

WGK Allemagne

3

RTECS

DC2975000

Poids moléculaire

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
    • Classe Phenol ethers
      • Subclass Anisoles

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: 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
• Description: 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

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Soluble in chloroform, methanol.
• Sensibilité: Light Sensitive
• Point d'ébullition (°C): 296°C
• Point de fusion (°C): 57-61°C
• Poids moléculaire: 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