122372-27-4 Usage
Uses
Used in Pharmaceutical Synthesis:
N-Allyl-N'-(2-cyanophenyl)urea is used as a reactive intermediate for the synthesis of various pharmaceutical compounds. Its unique chemical structure allows it to be incorporated into a wide range of drug molecules, enhancing their therapeutic properties and effectiveness.
Used in Agrochemical Synthesis:
In the agrochemical industry, N-Allyl-N'-(2-cyanophenyl)urea is utilized as a key intermediate in the production of various agrochemicals, such as pesticides and herbicides. Its ability to form stable compounds with other molecules makes it a valuable component in the development of effective and environmentally friendly agrochemicals.
Used as a Catalyst in Chemical Reactions:
N-Allyl-N'-(2-cyanophenyl)urea can act as a catalyst in a variety of chemical reactions, facilitating the formation of desired products and improving the efficiency of the reaction process. Its versatility as a catalyst makes it a valuable tool in organic synthesis and other chemical applications.
Used in Antimicrobial and Antifungal Applications:
Due to its potential biological and pharmacological activities, N-Allyl-N'-(2-cyanophenyl)urea has been studied for its antimicrobial and antifungal properties. It can be used as an active ingredient in various antimicrobial and antifungal formulations, helping to combat infections and protect against microbial contamination in various settings.
Overall, N-Allyl-N'-(2-cyanophenyl)urea is a versatile and valuable compound with a wide range of applications in the pharmaceutical, agrochemical, and chemical industries, as well as in the development of antimicrobial and antifungal products. Its unique properties and potential for further research and development make it an important component in the advancement of various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 122372-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,3,7 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 122372-27:
(8*1)+(7*2)+(6*2)+(5*3)+(4*7)+(3*2)+(2*2)+(1*7)=94
94 % 10 = 4
So 122372-27-4 is a valid CAS Registry Number.
122372-27-4Relevant articles and documents
Imidazo(1,2-c)quinazoline derivates as antihyper tensives and anti dysurics
-
, (2008/06/13)
Compounds of formula wherein:, X is O or S;, R1 is hydrogen, alkyl, phenyl or phenyl(alkyl);, R2 is hydrogen, alkyl, phenyl or phenyl(alkyl); or R1 and, R2 together represent alkylene or wherein R5 re
Studies on Quinazolines. 5. 2,3-Dihydroimidazoquinazoline Derivatives: A Novel Class of Potent and Selective α1-Adrenoceptor Antagonists and Antihypertensive Agents
Chern, Ji-Wang,Tao, Pao-Luh,Yen, Mao-Hsiung,Lu, Guan-Yu,Shiau, Chia-Yang,et al.
, p. 2196 - 2207 (2007/10/02)
A series of 2-- and 2--2,3-dihydroimidazoquinazolin-5(6H)-ones or -5(6H)-thiones, and 3--2,3-dihydroimidazoquinazol
2-substituted methyl-2,3-dihydroimidazo[1,2-c]quinazolin-5(6H)-ones (thiones), the preparation and use thereof
-
, (2008/06/13)
The present invention provides a novel series of 2-substituted methyl-2,3-dihydroimidazo[1,2-c]quinazolin-5(6H)-ones (-thiones) compounds. These compounds are found useful as an active ingredient for the prophylaxis and treatment of hypertension.
CATALASE-MEDIATED CYCLIZATION: SYNTHESIS OF 3-ALLYL-4-IMINO SUBSTITUTED 2(1H)-QUINAZOLINONES AND 1,3-BENZOXAZINE-2(3H)-ONES
Kamal, Ahmed,Sattur, P. B.
, p. 1133 - 1134 (2007/10/02)
The cyclization of N-allyl carbamoyl anthranilonitriles as well as O-allylcarbamoyl salicylonitrile to 2(1H)-quinazolinones and 1,3-benzoxazine-2(3H)-ones in quantitative yields by employing catalase has been described.
A Novel Enzymatic Cyclization: Synthesis of Imidazo-fused Quinazolinones by Baker's Yeast
Amal, Ahmed,Sattur, Prahlad B.
, p. 835 - 836 (2007/10/02)
Baker's yeast-mediated double cyclization of N-allylcarbamoylanthranilonitriles to 2-methylimidazoquinazolin-5(3H)-ones is described.
