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1(2H)-Naphthalenone, 3,4-dihydro-2-(4-hydroxyphenyl)-, also known as 2-(4-hydroxyphenyl)-3,4-dihydro-1(2H)-naphthalenone, is an organic compound with the molecular formula C15H12O2. It is a derivative of naphthalenone, featuring a naphthalene ring with a ketone group at position 1 and a 4-hydroxyphenyl group attached at position 2. 1(2H)-Naphthalenone, 3,4-dihydro-2-(4-hydroxyphenyl)- is characterized by its unique structure, which combines the properties of both naphthalene and phenol. It is often used in the synthesis of various pharmaceuticals, dyes, and other organic compounds due to its versatile chemical properties. The compound is typically synthesized through a series of chemical reactions, such as Friedel-Crafts acylation or other similar processes, and is an important intermediate in organic chemistry.

3261-93-6

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3261-93-6 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

Describes the physical state and color of the compound.

Explanation

Indicates that the compound has a noticeable and recognizable smell.

Explanation

Lists the primary applications of the compound in the industry and research.

Explanation

Describes the compound's ability to neutralize harmful molecules and reduce inflammation.

Explanation

Suggests that the compound has been studied for its possible therapeutic effects on these specific medical conditions.

Explanation

Indicates that the compound can be used as a starting material to create other chemical compounds.

Explanation

Emphasizes the importance of proper handling and safety measures due to potential hazards and toxic effects.

Explanation

Warns of the compound's potential negative impact on health and the environment.

Appearance

White crystalline solid

Odor

Distinct

Usage

Production of pharmaceuticals and as a research chemical

Properties

Antioxidant and anti-inflammatory

Potential Medical Applications

Treatment of cancer and neurodegenerative diseases

Role in Synthesis

Potential precursor in the synthesis of other organic compounds

Safety Precautions

Handle with care and in accordance with safety guidelines

Potential Hazards

Toxic effects

Check Digit Verification of cas no

The CAS Registry Mumber 3261-93-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,6 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3261-93:
(6*3)+(5*2)+(4*6)+(3*1)+(2*9)+(1*3)=76
76 % 10 = 6
So 3261-93-6 is a valid CAS Registry Number.

3261-93-6Relevant academic research and scientific papers

A novel class of potential central nervous system agents. 3-Phenyl-2-(1-piperazinyl)-5H-1-benzazepines

Hino,Nagai,Uno,Masuda,Oka,Karasawa

, p. 107 - 117 (2007/10/02)

A series of 3-phenyl-2-piperazinyl-5H-1-benzazepines and related compounds were synthesized and evaluated for potential neuroleptic activity. The preparation of these compounds was carried out by 2,3-dichlorination of 3-phenyl-2,3,4,5-tetrahydro-1H-1-benz

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