726419

2-(Chlormethyl)-naphthalin

≥97.0%

• Synonym(e): β-Naphthylmethyl chloride, 2-Menaphthyl chloride, 2-Naphthylmethyl chloride
• Empirische Formel (Hill-System): C₁₁H₉Cl
• CAS-Nummer: 2506-41-4
• Molekulargewicht: 176.64
• Beilstein: 742185
• EG-Nummer: 219-713-5
• MDL-Nummer: MFCD00046488
• UNSPSC-Code: 12352100
• PubChem Substanz-ID: 329764234
• NACRES: NA.22

Eigenschaften

• Qualitätsniveau: 100
• Assay: ≥97.0% (GC); ≥97.0%; 97.0-103.0% (T)
• Form: crystals
• Funktionelle Gruppe: chloro
• SMILES String: ClCc1ccc2ccccc2c1
• InChI: 1S/C11H9Cl/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7H,8H2
• InChIKey: MPCHQYWZAVTABQ-UHFFFAOYSA-N

Beschreibung

Anwendung

• Improving insulin sensitivity: Research highlights dihydroberberine′s capacity to enhance insulin sensitivity through AMPK activation, offering a promising therapeutic strategy for managing insulin resistance and type 2 diabetes (Lewis and Falk, 2022).



• Anti-inflammatory effects: A study conducted on the anti-inflammatory properties of dihydroberberine found significant reductions in inflammatory markers, suggesting its potential as an anti-inflammatory agent in metabolic syndrome (Dian et al., 2022).



• Enhancing bioavailability: Investigations into the oral bioavailability of dihydroberberine demonstrate improvements over its precursor berberine, highlighting its superior pharmacokinetic profile which could lead to more effective clinical applications (Murakami, Bodor, and Bodor, 2023).



• Glucose uptake mechanisms: Studies on dihydroberberine have shown its effectiveness in facilitating glucose uptake, an essential function for metabolic health, through its interaction with cellular transport mechanisms (Moon et al., 2021).

Sicherheitshinweise

• Piktogramme: GHS05
• Signalwort: Danger
• H-Sätze: H314
• P-Sätze: P280 - P305 + P351 + P338 - P310
• Gefahreneinstufungen: Skin Corr. 1B
• Lagerklassenschlüssel: 8A - Combustible corrosive hazardous materials
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable