59863-61-5 Usage
Urea derivative
A compound based on the urea structure (CO(NH2)2)
1-tert-butyl-3-(2-methylbut-3-yn-2-yl)urea is derived from the urea structure, with modifications to the nitrogen atoms.
tert-Butyl group
A (CH3)3Cgroup attached to the nitrogen atom
The compound features a tert-butyl group, which is a bulky, three-methyl group attached to a carbon atom, connected to one of the nitrogen atoms in the urea structure.
2-Methylbut-3-yn-2-yl group
A (CH3)2CHC≡CH2 group attached to the nitrogen atom
The compound also contains a 2-methylbut-3-yn-2-yl group, which is an alkyne group with a methyl group and a propyne chain, attached to the other nitrogen atom in the urea structure.
Industrial and research applications
Use as a reagent in organic synthesis and as a building block for other compounds
1-tert-butyl-3-(2-methylbut-3-yn-2-yl)urea is employed in various industries and research settings, including its role as a reagent in organic synthesis and as a component in the preparation of other chemical compounds.
Pharmaceutical research and development
Potential drug candidate
The compound is also utilized in pharmaceutical research and development, as it may have potential as a drug candidate for various medical applications.
Unique structure
Valuable tool for scientists and chemists
The distinctive structure of 1-tert-butyl-3-(2-methylbut-3-yn-2-yl)urea makes it a valuable resource for scientists and chemists in their pursuit of new materials and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 59863-61-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,6 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59863-61:
(7*5)+(6*9)+(5*8)+(4*6)+(3*3)+(2*6)+(1*1)=175
175 % 10 = 5
So 59863-61-5 is a valid CAS Registry Number.
59863-61-5Relevant articles and documents
Metal-free 5-exo-dig cyclization of propargyl urea using TBAF
Huguenot, Florent,Delalande, Clémence,Vidal, Michel
, p. 4632 - 4635 (2014/12/11)
We present the first results of the intramolecular cyclization of propargyl ureas catalyzed by TBAF. Depending on the substituents close to the triple bond, imidazolone or methylene-imidazolidinone was obtained. The dual activation of the triple bond by interaction with TBAF via the cation-π is thought to be responsible.
