15597-76-9 Usage
Description
5-Chlorosalicylidene aniline, a member of the salicylidene aniline class, is a yellow solid with a molecular formula of C13H10ClNO2 and a molecular weight of 243.68 g/mol. It is known for its potential pharmacological and biological activities, including antimicrobial and antifungal properties, as well as its use in the synthesis of azo dyes and metal complexes. Its versatile chemical structure and properties make it a promising compound for various applications in fields such as pharmaceuticals, dyeing, and biotechnology.
Uses
Used in Pharmaceutical Industry:
5-Chlorosalicylidene aniline is used as a starting material for the synthesis of drugs targeting various diseases due to its potential pharmacological and biological activities.
Used in Dye Industry:
5-Chlorosalicylidene aniline is used as a precursor in the synthesis of azo dyes, which are widely used in the textile, paper, and leather industries for their colorfastness and variety of shades.
Used in Biotechnology:
5-Chlorosalicylidene aniline is used in the development of metal complexes, which have potential applications in catalysis, sensors, and imaging techniques.
Used in Antimicrobial Applications:
5-Chlorosalicylidene aniline is used as an antimicrobial agent, effective against a range of bacteria and fungi, making it suitable for use in disinfectants and preservatives.
Used in Antifungal Applications:
5-Chlorosalicylidene aniline is used as an antifungal agent, helping to prevent the growth of fungi in various settings, such as in agriculture and food preservation.
Check Digit Verification of cas no
The CAS Registry Mumber 15597-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,9 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15597-76:
(7*1)+(6*5)+(5*5)+(4*9)+(3*7)+(2*7)+(1*6)=139
139 % 10 = 9
So 15597-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H10ClNO/c14-11-6-7-13(16)10(8-11)9-15-12-4-2-1-3-5-12/h1-9,15H/b10-9-
15597-76-9Relevant articles and documents
Copper-Catalyzed Asymmetric Annulation Reactions of Carbenes with 2-Iminyl- or 2-Acyl-Substituted Phenols: Convenient Access to Enantioenriched 2,3-Dihydrobenzofurans
Liang, Xin-Shen,Li, Rui-Dong,Wang, Xiao-Chen
supporting information, p. 13885 - 13889 (2019/08/26)
We have developed a method for the highly diastereo- and enantioselective construction of 2,3-dihydrobenzofurans bearing tetrasubstituted carbon stereocenters by means of annulation reactions between carbenes and 2-iminyl- or 2-acyl-substituted phenols through catalysis by readily accessible copper(I)/bisoxazoline catalysts under mild conditions. These reactions feature a unique mechanism in which the copper catalyst serves a dual function: first it reacts with the diazo compound to generate a metal carbene, and second, upon formation of an oxonium ylide, it acts as a Lewis acid to activate the imine or ketone for diastereo- and enantioselective cyclization.
Synthesis and evaluation of copper complexes of Schiff-base condensates from 5-substituted-2-hydroxybenzaldehyde and 2-substituted-benzenamine as selective inhibitors of protein tyrosine phosphatases
Zhu, Ruiting,Lu, Liping,Zhu, Miaoli,Han, Hong,Yuan, Caixia,Xing, Shu,Fu, Xueqi
, p. 91 - 97 (2013/10/22)
Five copper complexes, [Cu(bhbb,chbb,nhbb)(H2O)n] (tridentate-ligands: H2bhbb = 2-(5-bromo-2-hydroxylbenzylideneamino) benzoic acid, 1; H2chbb = 2-(5-chloro-2-hydroxylbenzylideneamino) benzoic acid, 2; H2/
Synthesis and evaluation of oxovanadium(iv) complexes of Schiff-base condensates from 5-substituted-2-hydroxybenzaldehyde and 2-substituted- benzenamine as selective inhibitors of protein tyrosine phosphatase 1B
Han, Hong,Lu, Liping,Wang, Qingming,Zhu, Miaoli,Yuan, Caixia,Xing, Shu,Fu, Xueqi
, p. 11116 - 11124 (2012/10/30)
Five oxovanadium(iv) complexes, which were divided into two groups, [V IVO(bhbb, nhbb)(H2O)2] (tridentate ligands: H2bhbb = 2-(5-bromo-2-hydroxylbenzylideneamino)benzoic acid, 1; H2nhbb = 2-(5-nitro-2