Methoxybenzoquinone - ≥99%(GC) , CAS No.2880-58-2

CAS: 2880-58-2 Cat. No.: M140181 Summenformel: C₇H₆O₃ Molekulargewicht: 138.12 Beilstein Registry Number: 8(4)1733 EG-Nummer: 809-193-3

GRADE & PURITY ≥99%(GC)

Synonyms

2-Methoxy-p-benzoquinone | trimethyl-1,3-thiazole | BDBM50130360 | M1045 | Methyl beta-methiopropionate | p-Benzoquinone, methoxy | 2 -methoxy-p-benzoquinone | 2-methoxybenzoquinone | NCIOpen2_003694 | DTXSID00182991 | METHYL 4-(((6-CHLORO-5-NITROPYRIMIDI

Storage

Protected from light,Argon charged,Room temperature

Shipped In

Normal

Specifications

Synonyme

2-Methoxy-p-benzoquinone | trimethyl-1,3-thiazole | BDBM50130360 | M1045 | Methyl beta-methiopropionate | p-Benzoquinone, methoxy | 2 -methoxy-p-benzoquinone | 2-methoxybenzoquinone | NCIOpen2_003694 | DTXSID00182991 | METHYL 4-(((6-CHLORO-5-NITROPYRIMIDI

Spezifikationen & Reinheit

≥99%(GC)

Storage

Protected from light,Argon charged,Room temperature

Verschickt in

Normal

Reinheit

≥99%(GC)

Namen und Kennungen

• Pubchem Sid: 504755029
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504755029
• Kanonisches Lächeln: COC1=CC(=O)C=CC1=O
• IUPAC Name: 2-methoxycyclohexa-2,5-diene-1,4-dione
• InChIKey: ZJKWJHONFFKJHG-UHFFFAOYSA-N
• INCHI: 1S/C7H6O3/c1-10-7-4-5(8)2-3-6(7)9/h2-4H,1H3
• Isomere SMILES: COC1=CC(=O)C=CC1=O
• Molekulargewicht: 138.12
• Beilstein: 8(4)1733
• Reaxy-Rn: 2042663
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2042663&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Klasse Organooxygen compounds
      • Subclass Carbonyl compounds
        • Ebene5 Ketones
          • Ebene6 Cyclic ketones
            • Ebene7 Quinones
              • Ebene8 Benzoquinones
                • Ebene9 P-benzoquinones

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: Organooxygen compounds
• Subclass: Carbonyl compounds
• Intermediate Tree Nodes: Ketones - Cyclic ketones - Quinones - Benzoquinones
• Direct Parent: P-benzoquinones
• Alternative Parents: Vinylogous esters Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: P-benzoquinone - Vinylogous ester - Organic oxide - Hydrocarbon derivative - Aliphatic homomonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as p-benzoquinones. These are benzoquinones where the two C=O groups are attached at the 1- and 4-positions, respectively.
• 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.

DOI: 10.1186/s13321-016-0174-y

Zugehörige Ziele (menschlich)

EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)

Discover Target: EGFR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ERBB2 Tclin Receptor protein-tyrosine kinase erbB-2 (7851 Activities)

Discover Target: ERBB2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

IGF1R Tclin Insulin-like growth factor I receptor (8605 Activities)

Discover Target: IGF1R

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

KDR Tclin Vascular endothelial growth factor receptor 2 (20924 Activities)

Discover Target: KDR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

FLT4 Tclin Vascular endothelial growth factor receptor 3 (3216 Activities)

Discover Target: FLT4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TEK Tclin Tyrosine-protein kinase TIE-2 (3348 Activities)

Discover Target: TEK

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Zugehörige Ziele (nicht menschlich)

botA Botulinum neurotoxin type A (1303 Activities)

Discover Target: botA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Air sensitive.Light sensitive.
• Schmelzpunkt (°C): 145.0-149.0℃
• Molekulargewicht: 138.120 g/mol
• XLogP3: -0.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 138.032 Da
• Monoisotopic Mass: 138.032 Da
• Topological Polar Surface Area: 43.400 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 235.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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

Referenzen

1. Ruipeng Shen, Min Li, Shuo Wang, Yu-Mo Zhang, Sean Xiao-An Zhang.  (2025)  An electrochromic device based on dynamic coordination and the dissociation of Fe2+/Fe3+ and a leuco dye with an improved cycle life.  Journal of Materials Chemistry C,      [PMID:] [10.1039/D4TC04582C]