105512-82-1 Usage
General Description
4-(4-phenoxy-phenyl)-thiazol-2-ylamine is a chemical compound with the molecular formula C16H13N3OS. It is a thiazole derivative with a substituted phenoxy group. 4-(4-PHENOXY-PHENYL)-THIAZOL-2-YLAMINE has potential applications in pharmaceutical and agricultural industries due to its biological activities and potential as a drug lead. The thiazole ring and phenoxy group make it a promising candidate for modulating various biological pathways and targets in drug discovery. However, further research and studies are required to explore its full potential and effects on living organisms.
Check Digit Verification of cas no
The CAS Registry Mumber 105512-82-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,1 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 105512-82:
(8*1)+(7*0)+(6*5)+(5*5)+(4*1)+(3*2)+(2*8)+(1*2)=91
91 % 10 = 1
So 105512-82-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H12N2OS/c16-15-17-14(10-19-15)11-6-8-13(9-7-11)18-12-4-2-1-3-5-12/h1-10H,(H2,16,17)
105512-82-1Relevant articles and documents
Synthesis and Antimicrobial Activity of Some 2-aminothiazole and 2-aminothiadiazine Derivatives
Sar?güney, Ahmet Burak,Kocaba?, Erdal,Erci, Fatih,Torlak, Emrah,Co?kun, Ahmet
, p. 2107 - 2110 (2018)
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A rapid and high-yielding synthesis of thiazoles and aminothiazoles using tetrabutylammonium salts
Kocabas, Erdal,Sariguney, Ahmet Burak,Coskun, Ahmet
experimental part, p. 2849 - 2854 (2011/04/16)
A convenient method for the synthesis of thiazoles and aminothiazoles by treatment of phenacyl bromides with thioamides/thiourea in the presence of tetrabutylammonium hexafluorophosphate (Bu4NPF6) at room temperature was developed. The products having high yields were formed rapidly (within 15 min). The method is simple, rapid and practical, generating thiazole derivatives in excellent isolated yields. The structures of the newly synthesized products were identified by FT-IR, 1H NMR, 13C NMR spectroscopy and elemental analysis data. The Japan Institute of Heterocyclic Chemistry.
