1722-63-0 Usage
Description
(4-phenylbut-3-en-2-ylideneamino)urea, also known as a urea derivative, is a chemical compound with the molecular formula C12H14N2O. It features a phenyl group and a butene moiety attached to the amino group, which contributes to its potential biological activity and interest in medicinal chemistry.
Uses
Used in Medicinal Chemistry:
(4-phenylbut-3-en-2-ylideneamino)urea is used as a compound of interest for its potential biological activity, particularly in the field of drug discovery and development. The conjugated system of the butene moiety and the phenyl group in (4-phenylbut-3-en-2-ylideneamino)urea makes it a valuable compound for the synthesis of novel drugs with diverse pharmaceutical applications.
Used in Drug Synthesis:
In the pharmaceutical industry, (4-phenylbut-3-en-2-ylideneamino)urea is used as a key intermediate for the development of new drugs. Its unique structure allows for the creation of a variety of drug candidates that can target different biological pathways and diseases.
Further research and exploration of the properties and biological activities of (4-phenylbut-3-en-2-ylideneamino)urea are needed to fully understand its potential in the field of medicinal chemistry and to unlock its full range of applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1722-63-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1722-63:
(6*1)+(5*7)+(4*2)+(3*2)+(2*6)+(1*3)=70
70 % 10 = 0
So 1722-63-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H13N3O/c1-9(13-14-11(12)15)7-8-10-5-3-2-4-6-10/h2-8H,1H3,(H3,12,14,15)
1722-63-0Relevant articles and documents
Larvicidal studies of chalcones and their derivatives
Das,Begum,Choudhury,Banerji
, p. 161 - 164 (2007/10/03)
Chalcone (1,3-diphenyl-2-propen-1-one) is considered as the lead compound among all the chalcone type compounds used for the larvicidal studies, as it has the highest toxicity against the larvae of Culex quinquefasciatus. 4-Phenylbut-3-en-2-one, where a methyl group replaces the phenyl group of chalcone, is less active than chalcone; but still has higher activity than other derived compounds except the oxime of the same compound, while 1,5-diphenylpenta-1,4-dien-3-one (in which the lengthening of the acyclic conjugated portion occurs) has almost no activity at 100 ppm at an interval of 24 h. ANOVA and CD values of the compounds show that larvicidal activity of 4-phenylbut-3-en-2-one and its oxime is greater than its phenylhydrazone, which has, however, higher activity than that of semicarbazone of 4-phenylbut-3-en-2- one. On the other hand the activities of 1,5-diphenylpenta-1,4-dien-3-one itself and 2,4-dinitrophenylhydrazone of chalcone and chalcone type compounds are almost nil at 100 ppm concentration at an interval of 24 h at 30 ± 2°C. The probable explanation of the fall of larvicidal activities of these compounds has been presented.
