1,7-Dihydroxynaphthalene - ≥98%(GC) , CAS No.575-38-2

CAS: 575-38-2 Cat. No.: D156007 Summenformel: C₁₀H₈O₂ Molekulargewicht: 160.17 Beilstein Registry Number: 1908500 EG-Nummer: 209-383-0

GRADE & PURITY ≥98%(GC)

Synonyms

MFCD00035720 | A18920 | AKOS005444304 | AB01334083-02 | NSC 62686 | AC-24466 | DTXSID0060359 | Q27268099 | D87698 | NSC62686 | NSC-62686 | 1-Hydroxy-7-naphthol | EN300-194280 | SCHEMBL29616 | EINECS 209-383-0 | LCZC00013 | CCRIS 7895 | AS-12658 | STK36841

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyme

MFCD00035720 | A18920 | AKOS005444304 | AB01334083-02 | NSC 62686 | AC-24466 | DTXSID0060359 | Q27268099 | D87698 | NSC62686 | NSC-62686 | 1-Hydroxy-7-naphthol | EN300-194280 | SCHEMBL29616 | EINECS 209-383-0 | LCZC00013 | CCRIS 7895 | AS-12658 | STK36841

Spezifikationen & Reinheit

≥98%(GC)

Storage

Room temperature

Verschickt in

Normal

Reinheit

≥98%(GC)

Namen und Kennungen

• Pubchem Sid: 488184146
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488184146
• Kanonisches Lächeln: C1=CC2=C(C=C(C=C2)O)C(=C1)O
• IUPAC Name: naphthalene-1,7-diol
• InChIKey: ZUVBIBLYOCVYJU-UHFFFAOYSA-N
• INCHI: 1S/C10H8O2/c11-8-5-4-7-2-1-3-10(12)9(7)6-8/h1-6,11-12H
• Isomere SMILES: C1=CC2=C(C=C(C=C2)O)C(=C1)O
• WGK Deutschland: 2
• RTECS: QJ4746666
• Molekulargewicht: 160.17
• Beilstein: 1908500
• Reaxy-Rn: 1908499
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1908499&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Naphthalenes
      • Subclass Naphthols and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Naphthalenes
• Subclass: Naphthols and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Naphthols and derivatives
• Alternative Parents: 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: 1-naphthol - 2-naphthol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as naphthols and derivatives. These are naphthalene derivatives carrying one or more hydroxyl (-OH) groups at any ring position.
• 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

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IDO1 Tchem Indoleamine 2,3-dioxygenase (6650 Activities)

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: Slightly soluble in water.
• Flammpunkt (°F): 485.6 °F
• Flammpunkt (°C): 252 °C
• Schmelzpunkt (°C): 175 °C
• Molekulargewicht: 160.170 g/mol
• XLogP3: 1.900
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 160.052 Da
• Monoisotopic Mass: 160.052 Da
• Topological Polar Surface Area: 40.500 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 158.000
• 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. Xingzhong Chen, Fang Yan, Jiurong Li, Xiao Gong.  (2025)  Control Synthesis of Multicolor Emitting Carbonized Polymer Dots Using Different Dihydroxynaphthalene Isomers.  JACS Au,      [PMID:40151271] [10.1021/jacsau.4c01220]