54255-11-7 Usage
Description
1H-Imidazole, 2-chloro-4,5-dihydro-, with the molecular formula C3H5ClN2, is a chemical compound derived from imidazole, featuring a five-membered ring with two nitrogen atoms. The unique addition of a chloro group at the 2nd position and dihydro groups at the 4th and 5th positions endows this compound with distinctive properties. It serves as a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and functional materials, as well as a reagent in various chemical reactions.
Uses
Used in Pharmaceutical Industry:
1H-Imidazole, 2-chloro-4,5-dihydrois used as a key intermediate in the synthesis of various pharmaceuticals for its ability to form complex organic molecules with potential therapeutic properties.
Used in Agrochemical Industry:
1H-IMidazole, 2-chloro-4,5-dihydrois utilized as a precursor in the development of agrochemicals, contributing to the creation of effective pesticides and other agricultural products to enhance crop protection and yield.
Used in Material Science:
1H-Imidazole, 2-chloro-4,5-dihydrois employed in the production of certain functional materials due to its structural and chemical properties that allow for the engineering of materials with specific applications.
Used as a Chemical Reaction Reagent:
1H-IMidazole, 2-chloro-4,5-dihydroserves as a reagent in a variety of chemical reactions, facilitating the synthesis of diverse organic molecules for research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 54255-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,5 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54255-11:
(7*5)+(6*4)+(5*2)+(4*5)+(3*5)+(2*1)+(1*1)=107
107 % 10 = 7
So 54255-11-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H5ClN2/c4-3-5-1-2-6-3/h1-2H2,(H,5,6)
54255-11-7Relevant articles and documents
C-N Bond forming reactions in the synthesis of substituted 2-aminoimidazole derivatives
Gomez-SanJuan, Asier,Botija, Jose Manuel,Mendez, Almudena,Sotomayor, Nuria,Letea, Esther
, p. 44 - 56 (2014/03/21)
Carbon-nitrogen bond forming reactions oriented to the synthesis of 2-amino-imidazolidines and imidazoles have been investigated. The C-2 amination of imidazolidinones, via the corresponding 2-chlorodihydroimidazoles, led to 2-benzylaminodihydroimidazole or bis(dihydroimidazole)amino derivatives by choosing the adequate experimental conditions. On the other hand, the use of N-acyl-2-methylsulfanyldihydroimidazoles allowed carrying out the reactions with aromatic amines, such as p-anisidine. Finally, palladium catalyzed Buchwald- Hartwig amination was the method of choice for C-N coupling between 2-haloimidazoles and aromatic amines in the synthesis of the corresponding imidazoles.
Efficient synthesis of 2-(N-Substituted)-2-imidazolines and 2-(N-Substituted)-1,4,5, 6-tetrahydropyrimidines
Kan, Wai Ming,Lin, Shih-Hsun,Chern, Ching-Yuh
, p. 2633 - 2639 (2007/10/03)
A general method for the preparation of 2-(N-Substituted)-2-imidazolines and 2-(N-Substituted)-1,4,5,6-tetrahydropyrimidines is described. These heterocycles can be synthesized from their respective anilines with 2-chloro-2-imidazoline or 2-chloro-1,4,5,6-tetrahydropyrimidine, generated in situ from imidazolidin-2-one and tetrahydropyrimidin-2(1H)-one activated by dimethyl chlorophosphate, in good to excellent yields. Copyright Taylor & Francis, Inc.
THIOPHENYLAMINOIMIDAZOLINES
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Page/Page column 29-30, (2010/02/10)
Methods for treatment of IP antagonist mediated diseases or conditions by administration to a subject in need thereof a compound of formula (I) wherein R1, R 2 , A and X are as defined herein. Also disclosed are compounds and related compositions.