15548-89-7 Usage
General Description
Phenol, 4-(1H-imidazol-2-yl)-, also known as 4-(1H-imidazol-2-yl)phenol, is a chemical compound with the molecular formula C9H8N2O. It is a derivative of phenol that contains an imidazole ring, which is a five-membered heterocyclic ring containing nitrogen. This chemical is commonly used in the pharmaceutical industry as an intermediate in the synthesis of various drugs, including antifungal and antiviral medications. It has also been studied for its potential as a ligand in coordination chemistry and as a building block in organic synthesis. Additionally, 4-(1H-imidazol-2-yl)phenol has applications in the field of biochemical research and has been investigated for its potential biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 15548-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,4 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15548-89:
(7*1)+(6*5)+(5*5)+(4*4)+(3*8)+(2*8)+(1*9)=127
127 % 10 = 7
So 15548-89-7 is a valid CAS Registry Number.
15548-89-7Relevant articles and documents
Reactivity of hydroxy and amino derivatives of 2-phenyl-1H-imidazoline and 2-phenyl-1H-imidazole toward isocyanates: Synthesis of appropriate carbamates and ureas
Parik, Patrik,Jansa, Josef,Holesova, Sylva,Marek, Ales,Klimesova, Vera
, p. 903 - 910 (2013/08/23)
Reactivity of 2-(4-hydroxyphenyl)-1H-imidazoline and 2-(4-hydroxyphenyl)- 1H-imidazole toward substituted phenyl isocyanates was studied. When mentioned imidazoline was treated with 2.5 equiv of substituted phenyl isocyanate, three N,O-dicarboxamides were
Synthesis and biological evaluation of novel 2-(4-O-β-D- glucosidoxyphenyl)-4,5-disubstituted imidazoles
Taile,Hatzade,Gaidhane,Ingle
experimental part, p. 903 - 907 (2010/10/18)
A series of 2-(4-hydroxyphenyl)-4,5-disubstituted imidazoles (1a-e) prepared from α-diketones, ammonium acetate, and p-hydroxybenzaldehyde, which were glucosylated by using α-acetobromoglucose to form 2-(4-O-β-D-2,3,4,6-tetra-O-acetyl-glucosidoxyphenyl)-4
