79662-84-3 Usage
Description
1-(2-cyanopropan-2-yl)urea, also known as N-cyanoprop-2-en-1-ylurea, is a chemical compound characterized by the molecular formula C5H8N2O. It is a urea derivative featuring a cyanoprop-2-en-1-yl functional group attached to the nitrogen atom, which endows it with unique chemical properties and potential applications across various scientific fields.
Uses
Used in Organic Synthesis:
1-(2-cyanopropan-2-yl)urea is utilized as a key building block in organic synthesis for the creation of various biologically active molecules. Its unique structure allows for the development of new compounds with potential applications in pharmaceuticals and other industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(2-cyanopropan-2-yl)urea serves as an important intermediate in the development of novel drugs. Its ability to form stable complexes with metal ions makes it a valuable component in the design and synthesis of metal-based therapeutic agents.
Used in Coordination Chemistry:
1-(2-cyanopropan-2-yl)urea is employed as a ligand in coordination chemistry, where it forms stable complexes with metal ions. These complexes have potential applications in various areas, including catalysis and materials science.
Used in Materials Science:
Due to its unique chemical properties, 1-(2-cyanopropan-2-yl)urea may find applications in the field of materials science. It could be used to develop new materials with specific properties, such as improved stability or reactivity.
Used in Catalysis:
1-(2-cyanopropan-2-yl)urea's ability to form complexes with metal ions also makes it a candidate for use in catalysis. It could potentially be employed in the development of new catalysts for various chemical reactions, enhancing the efficiency and selectivity of these processes.
Check Digit Verification of cas no
The CAS Registry Mumber 79662-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,6 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79662-84:
(7*7)+(6*9)+(5*6)+(4*6)+(3*2)+(2*8)+(1*4)=183
183 % 10 = 3
So 79662-84-3 is a valid CAS Registry Number.
79662-84-3Relevant articles and documents
The Reactions of Guanidine and Urea with Cyanohydrines
Wendelin, Winfried,Schramm, Hans-Wolfgang,Zmoelnig, Ilse
, p. 853 - 866 (2007/10/02)
Action of guanidine or urea on cyclohexanone-, cyclopentanone-, cycloheptanone- and acetonecyanohydrine 3a-3d generates very different products: 3a reacts with guanidine in DMF to yield 1,3-diazaspirodecane-2,4-diimine (5a).Heating the components without solvent affords 7,14-diazadispiropentadecan-15-one (7), the guanidine not participating in the reaction; similarly 3b is transformed by guanidine to a pentacyclic dispirocompound (possible formulae 19 and 20), whereas 3d reacts to give 3,3,5,5-tetramethylpiperazine-2,6-dion (21).In 3-pentanone guanidine- cyanide condensates itself to give 2,4-diamino-triazine (22).Action of urea on 3a-3d yields the 4-imino-1,3-diazaspiroalkan-2-ones 6a-6c and the 4-imino-5,5-dimethylimidazolidin-2-one 6d resp.If the reaction of urea and 3d is carried out in DMF, however, 5,5-dimethyl-4-ureido-3-imidazolin-2-one (28) (or the tautomeric carbamoyliminoimidazolidinone 27) is produced.The structures of the compounds prepared are proved by NMR-, IR- and mass spectra. - Keywords: 1.3-Diazaspiroalkan-2-ones. 4-imino; 1.3-Diazaspirodecan-2.4-diimine; Guanidine-cyanide. reactions with ketones; Guanidine. reactions with cyanohydrines; 2-Imidazolines, 4-imino-5.5-disubstituted; Urea. reactions with cyanohydrines
