129378-60-5 Usage
Explanation
Different sources of media describe the Explanation of 129378-60-5 differently. You can refer to the following data:
1. The compound consists of 6 carbon atoms, 12 hydrogen atoms, 4 nitrogen atoms, and 1 oxygen atom.
2. This name emphasizes the presence of three methyl groups attached to the imidazole ring and the酰胺 (carboxamide) functional group.
3. The compound is derived from imidazole, a five-membered heterocyclic ring containing two nitrogen atoms.
4. The compound forms a white, crystalline solid when in its pure form.
5. The compound can dissolve in aqueous and polar organic solvents due to its polar nature.
6. The unique structure and properties of the compound make it suitable for various applications in different industries.
7. The compound serves as a building block or reagent in the synthesis of various biologically active compounds and intermediates used in the pharmaceutical industry.
Physical appearance
White crystalline solid
Solubility
Soluble in water and polar organic solvents
Potential applications
Pharmaceuticals, agrochemicals, and other industries
Use in synthesis
Biologically active compounds and pharmaceutical intermediates
Check Digit Verification of cas no
The CAS Registry Mumber 129378-60-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,3,7 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 129378-60:
(8*1)+(7*2)+(6*9)+(5*3)+(4*7)+(3*8)+(2*6)+(1*0)=155
155 % 10 = 5
So 129378-60-5 is a valid CAS Registry Number.
129378-60-5Relevant articles and documents
Mechanistic investigations of the asymmetric hydrosilylation of ketimines with trichlorosilane reveals a dual activation model and an organocatalyst with enhanced efficiency
Li,Reeder,Torri,Adams,Jones
, p. 2422 - 2435 (2017/03/20)
Structural probes used to help elucidate mechanistic information of the organocatalyzed asymmetric ketimine hydrosilylation have revealed a new catalyst with unprecedented catalytic activity, maintaining adequate performance at 0.01 mol% loading. A new ‘dual activation’ model has been proposed that relies on the presence of both a Lewis basic and Br?nsted acidic site within the catalyst architecture.
2-Protecting Groups for 5-Lithiation in the Synthesis of Imidazoles
Ngochindo, Raphael I.
, p. 1645 - 1648 (2007/10/02)
Various substituents have been examined as possible 2-protecting groups against organolithium reagents in the syntheses of imidazoles on the basis of the ease of decarboxylation of imidazole-2-carboxylic acids and cleavage of the C(2)-Si bond.The tertiary
