59288-40-3 Usage
Uses
Used in Pharmaceutical Industry:
3-Pyridinecarboxylic acid, 5-hydroxy-6-iodo-, ethyl ester is used as an intermediate in the synthesis of pharmaceutical compounds for its unique structural features. The presence of the hydroxy and iodine atoms, along with the ethyl ester group, allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Pyridinecarboxylic acid, 5-hydroxy-6-iodo-, ethyl ester serves as a key component in the creation of novel agrochemicals. Its unique structure can be leveraged to develop new pesticides, herbicides, or other agricultural chemicals that can improve crop protection and yield.
Used in Organic Synthesis:
3-Pyridinecarboxylic acid, 5-hydroxy-6-iodo-, ethyl ester is used as a versatile building block in organic synthesis for its ability to be modified and incorporated into more complex organic molecules. Its structural features make it a valuable reagent for the development of new compounds with various applications in different industries.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-Pyridinecarboxylic acid, 5-hydroxy-6-iodo-, ethyl ester is utilized as a starting material for the design and synthesis of new pharmaceutical agents. Its unique functional groups can be exploited to create molecules with specific biological activities, potentially leading to the discovery of new drugs for the treatment of various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 59288-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,2,8 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59288-40:
(7*5)+(6*9)+(5*2)+(4*8)+(3*8)+(2*4)+(1*0)=163
163 % 10 = 3
So 59288-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8INO3/c1-2-13-8(12)5-3-6(11)7(9)10-4-5/h3-4,11H,2H2,1H3
59288-40-3Relevant academic research and scientific papers
A highly efficient solution and solid state ESIPT fluorophore and its OLED application
Trannoy, Virgile,Léaustic, Anne,Gadan, Sophie,Guillot, Régis,Allain, Clémence,Clavier, Gilles,Mazerat, Sandra,Geffroy, Bernard,Yu, Pei
, p. 3014 - 3021 (2021/02/26)
We present herein the synthesis and photophysics of 2,2′-bipyridine-3,3′-diol-5,5′-dicarboxylic acid ethyl ester (BP(OH)2DCEt2), an excited state intramolecular proton transfer (ESIPT)-based fluorophore featuring two identical intramolecular hydrogen bonds. BP(OH)2DCEt2emits efficiently not only in solution, including protic solvents (λem= 521 nm,Φf= 40 to 75%), but also in crystalline state (λem= 530 nm,Φf= 51%). In addition, its saponified form (Na2BP(OH)2DC) is highly fluorescent in water (λem= 490 nm,Φf= 51%). Finally, the good electroluminescence performance of BP(OH)2DCEt2is also demonstrated in an OLED device.
Synthesis method for 4-(tert-butoxycarbonyl) octahydrofuro[3,2-b] pyridine-6-carboxylic acid
-
Paragraph 0008; 0032; 0033, (2016/12/16)
The present incention relates to a synthesis method for 4-(tert-butoxycarbonyl) octahydrofuro[3,2-b] pyridine-6-carboxylic acid, and mainly solves the technical problem of no synthesis method suitable for industrialization at present. The synthesis method comprises six steps: first esterifying a compound 1 to obtain a compound 2; then performing iodination to produce a compound 3; acetylating the compound 3 to obtain a compound 4; then performing coupling to obtain a compound 5; performing cyclization to obtain a compound 6; performing hydrogenation to obtain a compound 7, then reacting with Boc anhydride to obtain a compound 8; and performing hydrogenation to obtain a final compound 9. The reaction formula is shown in the description.
