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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag für Lagerartikel Amorfrutin B - ≥97% , CAS No.78916-42-4
Synonyms
3-(3,7-dimethyloctyl)-2-hydroxy-4-methoxy-6-(2-phenylethyl)benzoic acid:3-[(2E)-3,7-dimethyl-2,6-octadien-1-yl]-2-hydroxy-4-methoxy-6-(2-phenylethyl)-benzoic acid | (E)-3-(3,7-Dimethylocta-2,6-dien-1-yl)-2-hydroxy-4-methoxy-6-phenethylbenzoic acid
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Übersicht Description
Isolated from Amorpha fruticosa.
Specifications Synonyme
3-(3,7-dimethyloctyl)-2-hydroxy-4-methoxy-6-(2-phenylethyl)benzoic acid:3-[(2E)-3,7-dimethyl-2,6-octadien-1-yl]-2-hydroxy-4-methoxy-6-(2-phenylethyl)-benzoic acid | (E)-3-(3,7-Dimethylocta-2,6-dien-1-yl)-2-hydroxy-4-methoxy-6-phenethylbenzoic acid
Spezifikationen & Reinheit
≥97%
Storage
Protected from light,Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Namen und Kennungen Kanonisches Lächeln
CC(=CCCC(=CCC1=C(C=C(C(=C1O)C(=O)O)CCC2=CC=CC=C2)OC)C)C
IUPAC Name
3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2-hydroxy-4-methoxy-6-(2-phenylethyl)benzoic acid
InChIKey
DKNIJLWIVUCTHW-CPNJWEJPSA-N
INCHI
1S/C26H32O4/c1-18(2)9-8-10-19(3)13-16-22-23(30-4)17-21(24(25(22)27)26(28)29)15-14-20-11-6-5-7-12-20/h5-7,9,11-13,17,27H,8,10,14-16H2,1-4H3,(H,28,29)/b19-13+
Isomere SMILES
CC(=CCC/C(=C/CC1=C(C=C(C(=C1O)C(=O)O)CCC2=CC=CC=C2)OC)/C)C
Alternative CAS-Nummer
1174387-94-0
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=27652250&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Phenylpropanoids and polyketides Klasse Stilbenes Subclass Not available Intermediate Tree Nodes Not available Direct Parent Stilbenes Alternative Parents P-methoxybenzoic acids and derivatives Aromatic monoterpenoids Salicylic acids Methoxyphenols Monocyclic monoterpenoids Benzoic acids Phenoxy compounds Methoxybenzenes Benzoyl derivatives Anisoles 1-hydroxy-4-unsubstituted benzenoids Alkyl aryl ethers Vinylogous acids Carboxylic acids Hydrocarbon derivatives Organic oxides Molecular Framework Aromatic homomonocyclic compounds Substituents Stilbene - P-methoxybenzoic acid or derivatives - Hydroxybenzoic acid - Methoxyphenol - Monocyclic monoterpenoid - Monoterpenoid - Aromatic monoterpenoid - Salicylic acid - Salicylic acid or derivatives - Benzoic acid or derivatives - Benzoic acid - Phenoxy compound - Anisole - Benzoyl - Phenol ether - Methoxybenzene - 1-hydroxy-4-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Monocyclic benzene moiety - Benzenoid - Vinylogous acid - Carboxylic acid derivative - Carboxylic acid - Ether - Organooxygen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound Beschreibung This compound belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. External Descriptors Not available 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.
3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Löslichkeit Soluble in DMSO, ethanol or methanol. Insoluble in water. Empfindlichkeit Light sensitive Flammpunkt (°F) Not applicable Flammpunkt (°C) Not applicable Molekulargewicht 408.500 g/mol XLogP3 7.600 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 10 Exact Mass 408.23 Da Monoisotopic Mass 408.23 Da Topological Polar Surface Area 66.800 Ų Heavy Atom Count 30 Formal Charge 0 Complexity 584.000 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
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