CAS 2348-82-5

2-Methoxy-1,4-naphthoquinone

Description:

2-Methoxy-1,4-naphthoquinone, with the CAS number 2348-82-5, is a synthetic organic compound characterized by its naphthoquinone structure, which features a methoxy group at the 2-position of the naphthalene ring. This compound typically appears as a yellow to orange solid and is known for its potential biological activities, including antioxidant properties and possible applications in medicinal chemistry. It is soluble in organic solvents such as ethanol and acetone but has limited solubility in water. The presence of the quinone functional group contributes to its reactivity, allowing it to participate in various chemical reactions, including redox processes. Additionally, 2-methoxy-1,4-naphthoquinone may exhibit cytotoxic effects against certain cancer cell lines, making it a subject of interest in pharmacological research. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks upon exposure. Overall, its unique structure and properties make it a valuable compound in both research and potential therapeutic applications.

Formula: C₁₁H₈O₃

InChI: InChI=1/C11H8O3/c1-14-10-6-9(12)7-4-2-3-5-8(7)11(10)13/h2-6H,1H3

InChI key: InChIKey=OBGBGHKYJAOXRR-UHFFFAOYSA-N

SMILES: O=C1C=2C(C(=O)C=C1OC)=CC=CC2

Synonyms:

• 1,4-Naphthalenedione, 2-Methoxy-
• 1,4-Naphthoquinone, 2-methoxy-
• 2-Methoxy-1,4-Naphthoquinone
• 2-Methoxy-1,4-dihydronaphthalene-1,4-dione
• 2-Methoxy-1,4-naphthalenedione
• 2-Methoxy-p-naphthoquinone
• 2-Methoxynaphthoquinone
• Lawsone methyl ether
• NSC 31530
• O-Methyllawsone
• 2-methoxynaphthalene-1,4-dione
• 2-methoxy-4-naphthalenedione
• 2-Methoxy-1,4-naphtoquinone
• 2-METHOXY-1,4-NAPTHOQUINONE, 98+% SEE S 45484-2
• 2-Methoxy-1,4-naphthoquinone 98%

1,4-NAPHTHALENEDIONE, 2-METHOXY-

CAS: 2348-82-5

Formula: C₁₁H₈O₃

Purity: 99%

Color and Shape: Solid

Molecular weight: 188.1794

Ref: IN-DA002NDL

Lawsone methyl ether

CAS: 2348-82-5

2-Methoxy-1,4-naphthoquinone triggers A549 cell apoptosis via JNK/p38 MAPK pathways, independent of cell cycle arrest, due to oxidative DNA damage from ROS.

Formula: C₁₁H₈O₃

Purity: 99.32% - 99.68%

Color and Shape: Yellow Solid

Molecular weight: 188.18

Ref: TM-T3008

Lawsone methyl ether

CAS: 2348-82-5

Lawsone methyl ether

Formula: C₁₁H₈O₃

Purity: ≥98%

Molecular weight: 188.18

Ref: 54-BUP16704

2-Methoxy-1,4-Naphthoquinone

CAS: 2348-82-5

2-Methoxy-1,4-Naphthoquinone

Purity: 95%

Molecular weight: 188.18g/mol

Ref: 54-OR1010516

Lawsone methyl ether

CAS: 2348-82-5

2-Methoxynaphthalene-1,4-dione

Formula: C₁₁H₈O₃

Purity: 99%

Molecular weight: 188.18

Ref: IN-DG76304

2-methoxy-1,4-naphthoquinone

CAS: 2348-82-5

Formula: C₁₁H₈O₃

Molecular weight: 188.18

Ref: 4Z-N-087012

1,4-NAPHTHALENEDIONE, 2-METHOXY-

CAS: 2348-82-5

Purity: ≥97%

Molecular weight: 188.1820068

Ref: 10-F828499

2-Methoxy-1,4-naphthoquinone

CAS: 2348-82-5

2-Methoxy-1,4-naphthoquinone is a natural compound that has low potency and significant cytotoxicity. It inhibits the polymerase chain reaction (PCR) by inhibiting DNA synthesis in the bacteria. This compound also exhibits antiinflammatory activity which may be due to its ability to inhibit prostaglandin synthesis. 2-Methoxy-1,4-naphthoquinone has been shown to exhibit minimal toxicity in mice and humans. It is structurally similar to p-hydroxybenzoic acid, a common ingredient found in food and cosmetics. 2-Methoxy-1,4-naphthoquinone has been used for the treatment of infectious diseases such as oral pathogens and bacterial infections caused by Helicobacter pylori or c. glabrata.

Formula: C₁₁H₈O₃

Purity: Min. 95%

Molecular weight: 188.18 g/mol

Ref: 3D-CAA34882