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1-Naphthalenol, 4-methoxy-2-methyl-, acetate is an organic compound with the chemical formula C13H14O3. It is a derivative of 1-naphthol, featuring a methyl group at the 2-position and a methoxy group at the 4-position. 1-Naphthalenol, 4-methoxy-2-methyl-, acetate is characterized by its aromatic structure, with a naphthalene ring system and an alcohol group. The acetate group is attached to the hydroxyl group, forming an ester. It is used in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical properties and reactivity. The compound is also known for its potential applications in the fragrance industry, contributing to the scent of certain perfumes and colognes. Its chemical structure and functional groups make it a versatile building block in organic synthesis, with potential uses in the development of new compounds with specific therapeutic or pesticidal properties.

3526-72-5

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3526-72-5 Usage

Physical state

Colorless liquid

Odor

Sweet, floral

Uses

Fragrance ingredient in cosmetics, perfumes, and personal care products; solvent; intermediate in manufacturing other chemicals

Hazards

Harmful if ingested, inhaled, or comes into contact with skin or eyes; may cause respiratory and skin irritation; toxic to aquatic organisms

Handling and storage

Handle and store carefully to avoid exposure and potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 3526-72-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,2 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3526-72:
(6*3)+(5*5)+(4*2)+(3*6)+(2*7)+(1*2)=85
85 % 10 = 5
So 3526-72-5 is a valid CAS Registry Number.

3526-72-5Downstream Products

3526-72-5Relevant academic research and scientific papers

The regioselective synthesis of monomethoxynaphthylene diacetates

Maiti, Bhim C.,Musgrave, Oliver C.,Skoyles, Douglas

, p. 1765 - 1771 (2007/10/03)

Methods for the conversion of 1,4,5-naphthalenetriols into the corresponding monomethoxy diacetates are described. All utilise the formation of peri-bridged intermediates.

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