13343-92-5 Usage
Description
METHYL 2-METHOXY-1-NAPHTHOATE is a chemical compound with the molecular formula C13H12O3. It is an ester of methoxy-1-naphthoic acid and is known for its sweet, floral odor.
Used in Fragrance Industry:
METHYL 2-METHOXY-1-NAPHTHOATE is used as a fragrance ingredient for its characteristic sweet, floral scent. It is commonly used in perfumes, soaps, and other personal care products to provide a pleasant aroma.
Used in Flavor Industry:
METHYL 2-METHOXY-1-NAPHTHOATE is used as a flavor ingredient to impart a sweet, floral taste to various food and beverage products.
Used in Pharmaceutical Industry:
METHYL 2-METHOXY-1-NAPHTHOATE is used as a raw material in the production of pharmaceuticals due to its versatile chemical properties.
Used in Dye Industry:
METHYL 2-METHOXY-1-NAPHTHOATE is used as a component in the synthesis of dyes, contributing to the color and stability of the final product.
Used in Food and Beverage Industry:
METHYL 2-METHOXY-1-NAPHTHOATE is used as an antioxidant and stabilizer in food and beverage products to prevent oxidation and extend shelf life.
Check Digit Verification of cas no
The CAS Registry Mumber 13343-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,4 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13343-92:
(7*1)+(6*3)+(5*3)+(4*4)+(3*3)+(2*9)+(1*2)=85
85 % 10 = 5
So 13343-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H12O3/c1-15-11-8-7-9-5-3-4-6-10(9)12(11)13(14)16-2/h3-8H,1-2H3
13343-92-5Relevant articles and documents
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Warren,Gindy,Baddar
, p. 687 (1941)
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Decarbonylative halogenation by a vanadium complex
Rana, Sujoy,Haque, Rameezul,Santosh, Ganji,Maiti, Debabrata
, p. 2927 - 2932 (2013/04/24)
Metal-catalyzed halogenation of the C-H bond and decarbonylation of aldehyde are conventionally done in nature. However, metal-mediated decarbonylative halogenation is unknown. We have developed the first metal-mediated decarbonylative halogenation reaction starting from the divanadium oxoperoxo complex K3V5+2(O 22-)4(O2-)2(μ-OH) (1). A concerted decarbonylative halogenation reaction was proposed based on experimental observations.
Barriers to rotation about the chiral axis of tertiary aromatic amides
Ahmed, Anjum,Bragg, Ryan A.,Clayden, Jonathan,Lai, Lai Wah,McCarthy, Catherine,Pink, Jennifer H.,Westlund, Neil,Yasin, Samreen A.
, p. 13277 - 13294 (2007/10/03)
The barrier to rotation about the aryl-carbonyl bond in 40 tertiary aromatic amides was determined by variable temperature NMR spectroscopy (for rapid rotations) or by following the interconversion of atropisomers (for slower rotations). Empirical guidelines to the rate of Ar-CO bond rotation in hindered tertiary aromatic amides, and hence the stability of the atropisomeric stereoisomers of axially chiral amides, are presented.
