1,2,4-Trimethoxy-5-propenylbenzol

1,2,4-Trimethoxy-5-(1-propenyl)benzene

HCID 17903

Grundinformationen

CAS
494-40-6
Standard-SMILES
CC=Cc1cc(OC)c(OC)cc1OC
InChIKey
RKFAZBXYICVSKP-UHFFFAOYSA-N
Summenformel
C12H16O3
Durchschnittliche Molmasse
208,25 g/mol
Monoisotopische Masse
208,10994437

Namen und Bezeichner

Bevorzugter Name
1,2,4-Trimethoxy-5-(1-propenyl)benzene
IUPAC
1,2,4-trimethoxy-5-prop-1-enylbenzene
Lokaler Name
1,2,4-Trimethoxy-5-propenylbenzol
Englischer Name
1,2,4-trimethoxy-5-propenylbenzene
Summenformel
C12H16O3
Molmasse
208.25

Namen und Synonyme

1,2,4-trimethoxy-5-prop-1-enylbenzene494-40-6Azaron1,2,4-Trimethoxy-5-(1-propenyl)benzeneDTXSID20197784RefChem:906651DTXCID00819492207-788-71,2,4-Trimethoxy-5-propenylbenzene1,2,4-trimethoxy-5-(prop-1-en-1-yl)benzenealpha-Asarone;trans-Asaronecis-1-Propenyl-2,4,5-trimethoxybenzene
Weitere Namen anzeigen
BETA-AZARONECIS-ANDTRANS-ASARONE1,4,5-Trimethoxy-2-(1-propenyl)benzene1-(1-Propenyl)-2,4,5-trimethoxybenzeneBenzene, 1,2,4-trimethoxy-5-(1-propen-1-yl)-
Benzene, 1,2,4-trimethoxy-5-(1Z)-1-propenyl-|?-AsaroneB-ASARONESCHEMBL940800orb12221032,4,5 trimethoxy phenyl propeneRKFAZBXYICVSKP-UHFFFAOYSA-NHMS3750A07

Datenbank-Bezeichner

CAS
494-40-6
PubChem CID
17903
DTXSID
DTXSID20197784
EC Number
207-788-7

Eigenschaften

Berechnete Struktureigenschaften

XLogP
3
Polarare Oberfläche (TPSA)
27,7 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
3
Frei drehbare Bindungen
4
Schwere Atome
15

Experimentelle und physikochemische Eigenschaften

SpringerMaterials PropertiesDiamagnetic susceptibility
FragrancesFragrance substance (cis-and trans-Asarone) -> IFRA amendment 40

Physikochemische Eigenschaften

Schmelzpunkt
67 °C · 67°C
Siedepunkt
296 °C · 296°C (estimate)
Dichte
1.165 · 1.1650
Brechungsindex
1.5683 · 1.5683 (estimate)
Geruch (Odor)
odorless
LogP
3.406 · 3.406 (est)

Chemie und Industrie

Pharmakologische Informationen

MeSH Pharmacological Classification · 2 Einträge

Drugs that selectively bind to but do not activate histamine H1 receptors, thereby blocking the actions of endogenous histamine. Included here are the classical antihistaminics that antagonize or prevent the action of histamine mainly in immediate hypersensitivity. They act in the bronchi, capillaries, and some other smooth muscles, and are used to prevent or allay motion sickness, seasonal rhinitis, and allergic dermatitis and to induce somnolence. The effects of blocking central nervous system H1 receptors are not as well understood.

Agents that are used to treat allergic reactions. Most of these drugs act by preventing the release of inflammatory mediators or inhibiting the actions of released mediators on their target cells. (From AMA Drug Evaluations Annual, 1994, p475)

Verwendung und Herstellung

IFRA Fragrance Standards · 6 Einträge

cis-and trans-Asarone

494-40-6:; Benzene, 1,2,4-trimethoxy-5-(1-propen-1-yl)- (unspecified isomer); (E)-and (Z)-2,4,5-Trimethoxypropen-1-yl benzene); 2883-98-9:; α-Asarone; trans-Asarone; Benzene, 1,2,4-trimethoxy-5-(1-propenyl)-, (E)-; trans-Isoasarone; 5273-86-9:; ß-Asarone; cis-ß-Asarone; Benzene, 1,2,4-trimethoxy-5-(1-propenyl)-, (Z)-; cis-Isoasarone

IFRA_STD_110.pdf

40

IFRA 51st Amendment - Guidance for the use of IFRA Standards

Prohibition: This material should not be used as a fragrance ingredient_Restriction: This material should be used only in the limited quantity as stated in the Standard

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