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Usage

Uses

Used in Fragrance Industry:
METHYL 3-METHOXY-2-NAPHTHOATE is used as a fragrance ingredient for its sweet, floral, and fruity aroma, contributing to the formulation of perfumes and personal care products.
Used in Flavor Industry:
In the flavor industry, METHYL 3-METHOXY-2-NAPHTHOATE is used as a flavoring agent, enhancing the taste and aroma of various food and beverage products.
Used in Pharmaceutical Industry:
METHYL 3-METHOXY-2-NAPHTHOATE is utilized as an intermediate in organic synthesis, playing a crucial role in the development of pharmaceuticals and other medicinal compounds.
Used in Industrial and Consumer Products:
METHYL 3-METHOXY-2-NAPHTHOATE can also be found in various industrial and consumer products, serving as a key component in their formulation and functionality.

InChI:InChI=1/C13H12O3/c1-15-12-8-10-6-4-3-5-9(10)7-11(12)13(14)16-2/h3-8H,1-2H3

Upstream product

• 92-70-6 3-Hydroxy-2-naphthoic acid 
• 74-88-4 methyl iodide 
• 186581-53-3 diazomethane 
• 93-04-9 2-Methoxynaphthalene 
• 124-38-9 carbon dioxide 

Downstream Products

• 854652-28-1 1-(3-methoxy-[2]naphthyl)-3-(2-methoxy-phenyl)-propane-1,3-dione 
• 412340-35-3 1-(3-methoxy-[2]naphthyl)-3-phenyl-propane-1,3-dione 
• 54965-50-3 2-Methyl-4H-naphtho<2,3-b>pyran-4-on 
• 1592-38-7 2-Naphthalenemethanol 
• 91-57-6 2-Methylnaphthalene 
• 856199-63-8 2-methoxy-3-(toluene-4-sulfonyloxymethyl)-naphthalene 
• 483-55-6 phthiocol 
• 924904-18-7 (+)-(S)-10,10'-dimethoxy-9,9'-biphenanthryl 
• 443911-29-3 (3-aminooxalyl-1-cyclohexylmethyl-2-methyl-1H-benzo[g]indol-4-yloxy)-acetic acid methyl ester 
• 443911-43-1 1-cyclohexylmethyl-2-carboethoxy-4-methoxybenz[g]indole 
• 443911-46-4 2-[(1-cyclohexylmethyl-2-methyl-1H-benz[g]indol-4-yl)oxy]acetic acid methyl ester 
• 443911-44-2 1-cyclohexylmethyl-2-hydroxymethyl-4-methoxybenz[g]indole 
• 443911-45-3 1-cyclohexylmethyl-2-methyl-4-methoxybenz[g]indole 
• 56679-88-0 3-methoxy-naphthalene-2-carbaldehyde 

Relevant academic research and scientific papers

Metalation of 2-heterosubstituted naphthalenes at the 1- or 3- position: Factors that may determine the regiochemistry

Upon metalation and subsequent electrophilic trapping, 2-fluoronaphthalene inevitably gives rise to regioisomeric mixtures in varying proportions, whereas 2-(trifluoromethyl)naphthalene undergoes deprotonation either at the 1- or the 3-position, depending on the choice of the reagent. On the other hand, 2-(trifluo-romethoxy)naphthalene and 2-methoxynaphthalene react exclusively at the 3-position when, respectively, sec-butylhthium and superbasic reagents are employed. Steric repulsion by the peri hydrogen in combination with crowding due to coordination of the lithium atom with the methoxy group disfavors attack at the 1-position. Georg Thieme Verlag Stuttgart.

Tetrazoles bonded to certain polycyclic aromatic systems and anti-allergic use thereof

Amides obtained by reaction of aminotetrazole and certain optionally substituted polycyclic aromatic acids are potent anti-allergic agents.