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1,2-Naphthalenedione, 8-methoxy-, also known as 8-Methoxy-1,2-naphthoquinone, is an organic compound with the chemical formula C11H8O3. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. 1,2-Naphthalenedione, 8-methoxy- is derived from the parent molecule 1,2-naphthoquinone, which is a type of quinone, and features an additional methoxy group attached to the 8th carbon atom. 1,2-Naphthalenedione, 8-methoxy- is used in various applications, including as an intermediate in the synthesis of dyes and pharmaceuticals, and as a reagent in chemical reactions. It is also known for its potential biological activities, such as antioxidant properties, and has been studied for its potential use in the development of new drugs and materials.

2275-94-7

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2275-94-7 Usage

Derivative

Naphthalenedione with a methoxy group attached at the 8th position

Usage

a. Organic synthesis
b. Building block in pharmaceuticals and agrochemicals production
c. Potential antioxidant and anticancer properties
d. Research for therapeutic applications
e. Intermediate in pigments, dyes, and specialty chemicals manufacturing

Structure

A naphthalene-based compound with a carbonyl group at the 1st and 2nd positions and a methoxy group at the 8th position

Chemical Properties

a. Reactivity with various reagents due to the presence of carbonyl and methoxy groups
b. Potential to form adducts or complexes with metal ions

Appearance

Likely a solid or crystalline structure based on its molecular weight and structure

Solubility

Likely soluble in organic solvents such as ethanol, methanol, or acetone, due to its nonpolar naphthalene core and polar functional groups

Thermal stability

May decompose or react at high temperatures, as is common with organic compounds containing carbonyl and methoxy groups

Chemical stability

Stable under normal conditions, but sensitive to strong acids, bases, or nucleophiles that could potentially react with the carbonyl or methoxy groups

Toxicity

Potentially toxic or harmful if ingested, inhaled, or absorbed through the skin

Hazardous decomposition products

May release toxic fumes or gases when heated or burned

Handling precautions

Use appropriate personal protective equipment (PPE) such as gloves, goggles, and lab coats when handling 1,2-Naphthalenedione, 8-methoxy-, and work in a well-ventilated area or fume hood

Environmental Impact

Potentially harmful to aquatic life and the environment if released in large quantities or improperly disposed of

Regulatory Information

May be subject to specific handling, storage, and disposal regulations depending on the jurisdiction and its intended use in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 2275-94-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,7 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2275-94:
(6*2)+(5*2)+(4*7)+(3*5)+(2*9)+(1*4)=87
87 % 10 = 7
So 2275-94-7 is a valid CAS Registry Number.

2275-94-7Upstream product

2275-94-7Downstream Products

2275-94-7Relevant academic research and scientific papers

Iodoxybenzene Oxidation of 1-Naphthols: Synthesis of Mansonone A

Murali, D.,Krishna Rao, G. S.

, p. 668 - 670 (2007/10/02)

Substituted 1-naphthols (1a-g) have been oxidized by iodoxybenzene to afford a mixture of the corresponding 1,2-(2a-g)-and 1,4-(3a-g)-naphthoquinones.Similar oxidation of a tetrahydro-8-naphthol (8-hydroxycalamenene) (4) gives mansonone-A (5) and a 1,4-quinone (6).During oxidation iodoxybenzene preserves intact labile structural features such as a benzylic tertiary hydroxyl group or a hydroaromatic ring.

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