68283-19-2 Usage
Uses
Used in Coordination Chemistry:
2-Butyl-5-hydroxymethylimidazole is used as a ligand in coordination chemistry for its ability to form stable complexes with various metal ions. This application is crucial in the development of new materials with specific properties, such as catalysts, sensors, and magnetic materials.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 2-Butyl-5-hydroxymethylimidazole is used as a key intermediate in the synthesis of various drugs. Its unique structure allows it to act as a building block for the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Synthesis:
Similarly, in the agrochemical sector, 2-Butyl-5-hydroxymethylimidazole is utilized as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness and selectivity in controlling pests and weeds.
Used in Corrosion Inhibition:
2-Butyl-5-hydroxymethylimidazole has potential applications in corrosion inhibition, where it can be used as an additive in various industrial processes to protect metal surfaces from corrosion. Its ability to form complexes with metal ions contributes to its effectiveness in this application.
Used as a Stabilizer in Plastic Materials:
In the plastics industry, 2-Butyl-5-hydroxymethylimidazole is used as a stabilizer to improve the durability and stability of plastic materials. Its incorporation can enhance the resistance of plastics to degradation, heat, and UV radiation, thereby extending their service life and performance.
Check Digit Verification of cas no
The CAS Registry Mumber 68283-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,8 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68283-19:
(7*6)+(6*8)+(5*2)+(4*8)+(3*3)+(2*1)+(1*9)=152
152 % 10 = 2
So 68283-19-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H14N2O/c1-2-3-4-8-9-5-7(6-11)10-8/h5,11H,2-4,6H2,1H3,(H,9,10)
68283-19-2Relevant academic research and scientific papers
Preparation of 2-Substituted 4-Chloro-5-Formylimidazole and 5-Formylimidazole
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Page/Page column 3, (2008/12/08)
The invention relates to a preparation process for 2-substituted 5-formylimidazoles, wherein the intermediate high-pressurized synthesis of an 2-substituted 4-hydroxymethylimidazole as known in the art is conveniently avoided, and wherein much higher yields are obtained. Instead, it is proposed to prepare such 2-substituted 5-formylimidazoles via a one-pot synthesis involving 2-substituted 4-chloro-5-formylimidazole, thereby employing an additional hydrodehalogenation step. Moreover, it is found that the yield and purity of 2-substituted 4-chloro-5-formylimidazole itself can be significantly improved using a triflate catalyst in the preparation process.
Substituted imidazolyl-alkylthio-alkanoic acids
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, (2008/06/13)
Angiotensin II receptor antagonists having the formula: STR1 which are useful in regulating hypertension and in the treatment of congestive heart failure, renal failure, and glaucoma, pharmaceutical compositions including these antagonists, and methods of using these compounds to produce angiotensin II receptor antagonism in mammals.
