54088-56-1 Usage
Urea derivative
1-tert-butyl-3-cyclohexylurea is a compound derived from urea, which means it has a similar structure to urea with some modifications.
tert-Butyl group
A tert-butyl group (C4H9) is attached to the urea molecule, contributing to the compound's structure and properties.
Cyclohexyl group
A cyclohexyl group (C6H11) is also attached to the urea molecule, providing a cyclic structure and additional properties to the compound.
Organic chemical compound
1-tert-butyl-3-cyclohexylurea is an organic compound, meaning it is primarily composed of carbon, hydrogen, and other non-metal elements.
Use as a catalyst
In organic synthesis, 1-tert-butyl-3-cyclohexylurea is commonly used as a catalyst to speed up chemical reactions and increase the yield of desired products.
Use as a reagent
The compound is also used as a reagent in various chemical reactions, facilitating the formation of new bonds or the transformation of reactants into products.
Applications in pharmaceuticals
1-tert-butyl-3-cyclohexylurea has a wide range of applications in the pharmaceutical industry, including the synthesis of drugs and the development of new therapeutic agents.
Applications in agriculture
The compound is also used in agriculture, potentially for the development of pesticides, herbicides, or other agrochemicals.
Applications in materials science
1-tert-butyl-3-cyclohexylurea can be used in the development of new materials, such as polymers, coatings, or other advanced materials with unique properties.
Unique structure and properties
The combination of the tert-butyl and cyclohexyl groups, along with the urea core, gives 1-tert-butyl-3-cyclohexylurea a unique structure that contributes to its versatility and value in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 54088-56-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,8 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54088-56:
(7*5)+(6*4)+(5*0)+(4*8)+(3*8)+(2*5)+(1*6)=131
131 % 10 = 1
So 54088-56-1 is a valid CAS Registry Number.
54088-56-1Relevant articles and documents
An easy access to unsymmetrical ureas: A photocatalytic approach to the Lossen rearrangement
Yadav, Arvind K.,Srivastava, Vishnu P.,Yadav, Lal Dhar S.
, p. 24498 - 24503 (2014/07/07)
An efficient and operationally simple method for the synthesis of unsymmetrical ureas from various hydroxamic acids and amines has been developed. Plausibly, the protocol involves visible-light-initiated in situ formation of Vilsmeier-Haack reagent and COBr2 with CBr4 and a catalytic amount of DMF in the presence of Ru(bpy)3Cl2 as a photocatalyst to bring about the Lossen rearrangement at room temperature. the Partner Organisations 2014.
The efficient synthesis of carbodiimides using a titanium imido complex
Anderson, James C.,Bou-Moreno, Rafael
experimental part, p. 9182 - 9186 (2011/01/12)
An efficient rt synthesis of carbodiimides or ureas from the combination of a titanium imido complex 2 and a range of 12 aryl and aliphatic isocyanates is described. Control experiments suggest that carbodimide formation is via heterocumulene metathesis t
