586959-21-9 Usage
Uses
Used in Pharmaceutical Applications:
1-(1H-INDOL-2-YLCARBONYL)-1H-BENZOTRIAZ& is used as a reagent in organic synthesis for its potential to contribute to the development of new pharmaceutical compounds. Its benzotriazole and indole moieties are of particular interest in drug discovery, as they may endow the compound with biological activity and therapeutic properties.
Used in Materials Science:
In the field of materials science, 1-(1H-INDOL-2-YLCARBONYL)-1H-BENZOTRIAZ& is utilized as a building block for the synthesis of various heterocyclic compounds, which are essential in creating advanced materials with specific properties.
Used as a Corrosion Inhibitor:
1-(1H-INDOL-2-YLCARBONYL)-1H-BENZOTRIAZ& is also recognized for its potential as a corrosion inhibitor, making it a valuable addition to the materials science field. Its ability to prevent or reduce the corrosion of metals can have significant implications for the longevity and maintenance of various industrial equipment and structures.
Used as a UV Absorber:
Furthermore, 1-(1H-INDOL-2-YLCARBONYL)-1H-BENZOTRIAZ& is employed as a UV absorber, which is crucial in protecting materials from the damaging effects of ultraviolet radiation. This application is particularly relevant in the manufacturing of coatings, plastics, and other materials that are exposed to sunlight or artificial UV sources.
Check Digit Verification of cas no
The CAS Registry Mumber 586959-21-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,6,9,5 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 586959-21:
(8*5)+(7*8)+(6*6)+(5*9)+(4*5)+(3*9)+(2*2)+(1*1)=229
229 % 10 = 9
So 586959-21-9 is a valid CAS Registry Number.
586959-21-9Relevant academic research and scientific papers
Preparation of polyfunctional acyl azides
Katritzky, Alan R.,Widyan, Khalid,Kirichenko, Kostyantyn
, p. 5802 - 5804 (2008/02/09)
(Chemical Equation Presented) A general synthesis of acyl azides from the corresponding N-acyl benzotriazoles is described. The procedure affords acyl azides in good yields and avoids the use of acid activators and NO+ equivalents typically emp
Efficient Conversion of Carboxylic Acids into N-Acylbenzotriazoles
Katritzky, Alan R.,Zhang, Yuming,Singh, Sandeep K.
, p. 2795 - 2798 (2007/10/03)
An improved one-pot procedure for the preparation of N-acylbenzotriazoles involves mild reaction conditions and allows the preparation of several derivatives not accessible by the previously reported methods.
Regiospecific C-acylation of pyrroles and indoles using N-acylbenzotriazoles
Katritzky, Alan R.,Suzuki, Kazuyuki,Singh, Sandeep K.,He, Hai-Ying
, p. 5720 - 5723 (2007/10/03)
Reactions of pyrrole (2) or 1-methylpyrrole (4) with readily available N-acylbenzotriazoles 1a - g (RCOBt, where R = 4-tolyl, 4-nitrophenyl, 4-diethylaminophenyl, 2-furyl, 2-pyridyl, 2-indolyl, or 2-pyrrolyl) in the presence of TiCl4 produced 2
