63449-68-3 Usage
Uses
Used in Scientific Research:
2-Aminobenzoic Acid Naphthalen-2-yl Ester is used as an organic intermediate for its ability to form complex structures, making it valuable in the synthesis of various compounds.
Used in Dye Production:
2-Aminobenzoic Acid Naphthalen-2-yl Ester is used as a component in the production of dyes due to its capacity to create intricate molecular structures, which contribute to the color and properties of the dyes.
Used in Experimental Procedures:
2-Aminobenzoic Acid Naphthalen-2-yl Ester is used as a synthetic reagent in various experimental procedures, facilitating the synthesis of new compounds and aiding in the advancement of scientific research.
Safety Precautions:
When handling 2-Aminobenzoic Acid Naphthalen-2-yl Ester, it is important to take precautionary measures such as wearing protective equipment to avoid inhalation and contact with skin or eyes, due to its strong aromatic odor and potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 63449-68-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,4 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63449-68:
(7*6)+(6*3)+(5*4)+(4*4)+(3*9)+(2*6)+(1*8)=143
143 % 10 = 3
So 63449-68-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H13NO2/c18-16-8-4-3-7-15(16)17(19)20-14-10-9-12-5-1-2-6-13(12)11-14/h1-11H,18H2
63449-68-3Relevant academic research and scientific papers
Ruthenium(ii)-catalyzed decarbonylative and decarboxylative coupling of isatoic anhydrides with salicylaldehydes: access to aryl 2-aminobenzoates
Bora, Bidisha R.,Prakash, Rashmi,Sultana, Sabera,Gogoi, Sanjib
, p. 2725 - 2730 (2021/04/07)
A ruthenium(ii)-catalyzed coupling reaction of isatoic anhydrides and salicylaldehydes has been developed for the synthesis of 2-aminobenzoates. This reaction proceeds through metal-catalyzed decarbonylation and decarboxylation to afford good yields of aryl 2-aminobenzoates.
Palladium-catalyzed decarboxylative coupling of isatoic anhydrides with arylboronic acids
Lu, Wei,Chen, Jiuxi,Liu, Miaochang,Ding, Jinchang,Gao, Wenxia,Wu, Huayue
supporting information; experimental part, p. 6114 - 6117 (2012/01/06)
The decarboxylative coupling of isatoic anhydrides with arylboronic acids was realized for the first time in the presence of Pd2(dba) 3 and DPEphos, achieving aryl o-aminobenzoates with yields ranging from moderate to good. The efficiency of this procedure was demonstrated by good compatibility with fluoro, chloro, bromo, nitro, cyano, trifluoromethyl, formacyl, acetyl, thienyl, and naphthyl groups. Preliminary mechanistic experiments using deuterium labeling showed that the oxygen atom was derived from dioxygen.
