2876-71-3 Usage
Uses
Used in Agricultural Industry:
Beta-Naphthylacetic acid, methyl ester is used as a plant growth regulator for its ability to stimulate root formation in a variety of plant species. It aids in enhancing fruit set and increasing overall crop yield, making it a valuable tool for managing plant growth and productivity in agriculture.
Used as a Foliar Spray:
In the agricultural application, Beta-Naphthylacetic acid, methyl ester is used as a foliar spray to promote plant growth. This method of application allows for the compound to be absorbed by the plant leaves, facilitating its effects on cell elongation and division.
Used for Cuttings:
Beta-Naphthylacetic acid, methyl ester is also used as a dip for cuttings. When applied in this manner, it encourages root development in the cuttings, improving their chances of successful growth and establishment.
Used in Plant Hormone Research:
In addition to its practical applications in agriculture, Beta-Naphthylacetic acid, methyl ester is utilized in research settings to study the effects of synthetic auxins on plant growth and development. This helps scientists to better understand the mechanisms of plant hormone action and to develop new strategies for crop improvement.
Check Digit Verification of cas no
The CAS Registry Mumber 2876-71-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,7 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2876-71:
(6*2)+(5*8)+(4*7)+(3*6)+(2*7)+(1*1)=113
113 % 10 = 3
So 2876-71-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H12O2/c1-15-13(14)9-10-6-7-11-4-2-3-5-12(11)8-10/h2-8H,9H2,1H3
2876-71-3Relevant academic research and scientific papers
Catalytic Carboxylation of Heteroaromatic Compounds: Double and Single Carboxylation with CO 2
Mita, Tsuyoshi,Masutani, Hiroki,Ishii, Sho,Sato, Yoshihiro
supporting information, p. 841 - 845 (2019/04/25)
In the presence of PdCl 2 [P(n -Bu) 3 ] 2 (10 mol%) and ZnEt 2, 2-furyl and 2-pyrrolylmethyl acetate were carboxylated with CO 2 (1 atm), affording doubly carboxylated products in good yields. In this dearomative transformation, α,?-dicarboxylic acids were obtained selectively, in contrast to our previous report in which α,γ-dicarboxylic acids were selectively produced from 2-indolylmethyl acetates. In contrast, 5-thiazolylmethyl acetate and naphthylmethyl acetates predominantly underwent single carboxylation.
Reduction of carboxylic acids using esters of benzotriazole as high-reactivity intermediates
Morales-Serna, Jose Antonio,Garcia-Rios, Erendira,Bernal, Jorge,Paleo, Ehecatl,Gavino, Ruben,Cardenas, Jorge
scheme or table, p. 1375 - 1382 (2011/06/19)
Herein, we describe a simple and practical protocol for the reduction of carboxylic acids via the in situ formation of hydroxybenzotriazole esters followed by reaction with sodium borohydride to give the corresponding alcohols. The reaction proceeds with excellent yields in the presence of water. Georg Thieme Verlag Stuttgart - New York.
