19276-01-8 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Butanone,4-(1H-benzimidazol-2-yl)-(9CI) is used as a key intermediate in the synthesis of pharmaceuticals for its potential biological activities. Its unique chemical structure allows for the development of new drugs with improved therapeutic properties.
Used in Dye Production:
In the dye industry, 2-Butanone,4-(1H-benzimidazol-2-yl)-(9CI) is used as a building block for the production of various dyes. Its aromatic structure contributes to the color and stability of the dyes, making it a valuable component in the synthesis process.
Used in Organic Chemistry Research:
2-Butanone,4-(1H-benzimidazol-2-yl)-(9CI) is utilized in organic chemistry research for its potential to participate in various organic reactions. Its unique properties make it a valuable tool for studying reaction mechanisms and developing new synthetic methods.
Used in Industrial Applications:
Due to its unique chemical structure and properties, 2-Butanone,4-(1H-benzimidazol-2-yl)-(9CI) may have potential industrial applications in various fields. Its versatility as a building block in organic chemistry reactions can contribute to the development of new materials and products with improved performance characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 19276-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,7 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19276-01:
(7*1)+(6*9)+(5*2)+(4*7)+(3*6)+(2*0)+(1*1)=118
118 % 10 = 8
So 19276-01-8 is a valid CAS Registry Number.
19276-01-8Relevant academic research and scientific papers
Serusi, Lorenzo,Soddu, Francesco,Cuccu, Federico,Peretti, Giuseppe,Luridiana, Alberto,Secci, Francesco,Caboni, Pierluigi,Aitken, David J.,Frongia, Angelo
, p. 4159 - 4163 (2020)
We have developed one-step protocols for the preparation of a large selection of α-aminocyclopropyl ketones or benzo[d]imidazoles, by reacting 2-substituted-2-hydroxycyclobutanones with aryl amines or o-phenylenediamines, respectively. In most case the reactions proceed at room temperature and are catalyst-free. The formation of benzo[d]imidazoles is rationalized in terms of an unusual ring-closure/ring-fission process followed by aromatization. (Figure presented.).
BENZAZEPIN-2(1H)-ONE DERIVATIVES
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Page/Page column 50, (2008/06/13)
Compounds of formula (I) and pharmaceutically acceptable salts thereof are agonists at the beta-2 adrenoceptor. They are useful as feed additives for livestock animals.
Reaction of 2-chloromethylbenzimidazoles with acetylacetone and benzoylacetone. Basic breakdown of β-diketones
Popov
, p. 918 - 922 (2007/10/03)
Base treatment of the products of alkylalion of β-diketones by 2-chloromethylbenzimidazole under phase transfer catalysis (PTC) conditions causes loss of the acetyl group and formation of methylethyl- or ethylphenyl ketones. 1997 Plenum Publishing Corpora
