53316-51-1 Usage
General Description
4,5-Dimethyl-1H-imidazole hydrochloride, also known as 4,5-Dimethylimidazole hydrochloride, is a chemical compound with the molecular formula C5H8N2.HCl. It is a derivative of imidazole, a five-membered heterocyclic ring containing two nitrogen atoms. 4,5-Dimethyl-1H-imidazole hydrochloride is commonly used as a reagent in organic synthesis, especially in the formation of pharmaceuticals and agrochemicals. It is also employed as a corrosion inhibitor and a stabilizer for photographic chemicals. Additionally, 4,5-Dimethyl-1H-imidazole hydrochloride has been investigated for its potential antimicrobial and antifungal properties, with applications in medicine and agriculture. Due to its versatile properties, this chemical is important for various industrial and research purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 53316-51-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,1 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53316-51:
(7*5)+(6*3)+(5*3)+(4*1)+(3*6)+(2*5)+(1*1)=101
101 % 10 = 1
So 53316-51-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N2.ClH/c1-4-5(2)7-3-6-4;/h3H,1-2H3,(H,6,7);1H
53316-51-1Relevant articles and documents
IONIC COMPOSITIONS AND RELATED USES THEREOF
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Page/Page column 19, (2018/09/21)
The present disclosure generally relates to ionic compositions which may be used in or as an adhesive material for selectively adhering two items together. More particularly, but not exclusively, the present disclosure relates to ionic compositions that include a cationic imidazolium compound and an anionic compound such as a sulfonyl imide compound.
Preparation of imidazoles
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, (2008/06/13)
Disclosed is a novel process and product involving the manufacture in advantageously high yields of imidazole compounds corresponding to the general formula: STR1 wherein a preferred embodiment of the process comprises contacting a diamine salt of the formula STR2 with a biscarbonyl compound of the structure STR3 in an acid medium, wherein R, R1 and R2 each represents hydrogen or any group which does not hinder the cyclization reaction or lead to degradation of the reactants or imidazole products, and A- is an anion equivalent such as that of mineral acids, sulfonic acids and carboxylic acids.
