3617-11-6 Usage
Heterocyclic aromatic organic compound
1H-Imidazole, 2,2'-(1,4-phenylene)bis[4,5-dihydrois a compound that contains a heterocyclic ring, which is a ring containing at least one atom that is not carbon, such as nitrogen in this case. This property gives it unique chemical and physical properties.
Derivative of imidazole
This compound is derived from imidazole, which is a five-membered ring structure containing three carbon atoms and two nitrogen atoms. The presence of this imidazole ring in the compound contributes to its chemical reactivity and potential applications.
Phenylene group
The compound contains a phenylene group, which is a benzene ring connected to two adjacent nitrogen atoms. This group is responsible for the compound's utility in the synthesis of certain drugs and biologically active molecules.
Use in pharmaceutical applications
1H-Imidazole, 2,2'-(1,4-phenylene)bis[4,5-dihydrois used in the pharmaceutical industry for the synthesis of various drugs and biologically active molecules due to its unique structure and reactivity.
Use in industrial applications
The compound is also used in industrial processes, such as the production of dyes and pigments, due to its chemical properties and structure.
Versatility
The combination of its structure, properties, and potential applications make 1H-Imidazole, 2,2'-(1,4-phenylene)bis[4,5-dihydroa versatile and important chemical in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 3617-11-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,1 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3617-11:
(6*3)+(5*6)+(4*1)+(3*7)+(2*1)+(1*1)=76
76 % 10 = 6
So 3617-11-6 is a valid CAS Registry Number.
3617-11-6Relevant articles and documents
Non-chelating p-phenylidene-linked bis-imidazoline analogs of known influenza virus endonuclease inhibitors: Synthesis and anti-influenza activity
Dar'in, Dmitry,Zarubaev, Vladimir,Galochkina, Anastasia,Gureev, Maxim,Krasavin, Mikhail
, p. 526 - 532 (2018/11/06)
A novel chemotype topologically similar to known influenza virus PA endonuclease inhibitors has been designed. It was aimed to reproduce the extended topology of the known metal-chelating ligands with a p-phenylidene-linked bis-imidazoline scaffold. It wa
Copper-catalyzed synthesis of 2-imidazolines and their N-hydroxyethyl derivatives under various conditions
Zhang, Jin,Wang, Xiao,Yang, Meipan,Wan, Kerou,Yin, Bing,Wang, Yunxia,Li, Jianli,Shi, Zhen
experimental part, p. 1578 - 1582 (2011/04/26)
A rapid and efficient method for the synthesis of 2-imidazolines and their N-hydroxyethyl derivatives from the reaction of aromatic nitriles with ethylenediamine (EDA) or N-(2-aminoethyl)ethanolamine (AEEA) using cupric indole-3-acetate (Cu(II)-(IAA)2) as a reusable catalyst under reflux and microwave conditions is reported. And seven new N-hydroxyethyl-imidazolines were reported for the first time.
Efficient catalytic synthesis of 2-imidazolines and bis-imidazolines with silica supported tungstosilicic acid
Nasr-Esfahani, Masoud,Montazerozohori, Morteza,Moghadam, Majid,Akhlaghia, Parisa
experimental part, p. 97 - 109 (2010/08/04)
A rapid and efficient preparation of 2-imidazolines and bis-imidazolines by the reaction of ethylenediamine or 1,2-propanediamine with nitriles in the presence of catalytic amounts of tungstosilicic acid supported on SiO 2 under reflux condition, is reported. The advantages of this procedure are moderate reaction times, good to high yields and the ability to carry out the large scale reactions. ARKAT USA, Inc.
