1119-61-5 Usage
Uses
Since the provided materials do not specify the applications of N-(3-Methoxypropyl)urea, I will list some potential uses based on its chemical properties and typical applications of similar compounds:
Used in Research and Development:
N-(3-Methoxypropyl)urea is used as a research compound for studying its unique properties and potential applications in various fields. Its chemical structure and reactivity make it a valuable tool for understanding the behavior of ureas and their derivatives.
Used in Chemical Synthesis:
N-(3-Methoxypropyl)urea can be used as a building block or intermediate in the synthesis of more complex organic compounds. Its functional groups, such as the amine and carbonyl groups, can participate in various chemical reactions, enabling the creation of new molecules with specific properties.
Used in Pharmaceutical Industry:
Due to its unique chemical structure, N-(3-Methoxypropyl)urea may have potential applications in the development of pharmaceuticals. It could be used as a starting material or a component in the synthesis of drug candidates, particularly those targeting specific biological pathways or receptors.
Used in Agrochemical Industry:
N-(3-Methoxypropyl)urea may also find applications in the agrochemical industry, where it could be used as a precursor or intermediate in the synthesis of pesticides, herbicides, or other agricultural chemicals. Its reactivity and functional groups may contribute to the development of new and effective products.
Check Digit Verification of cas no
The CAS Registry Mumber 1119-61-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1119-61:
(6*1)+(5*1)+(4*1)+(3*9)+(2*6)+(1*1)=55
55 % 10 = 5
So 1119-61-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H12N2O2/c1-9-4-2-3-7-5(6)8/h2-4H2,1H3,(H3,6,7,8)
1119-61-5Relevant articles and documents
Synthesis of novel 1-alkyl-8-substituted-3-(3-methoxypropyl) xanthines as putative A2B receptor antagonists
Nieto, Maria Isabel,Balo, Maria Carmen,Brea, Jose,Caamano, Olga,Cadavid, Maria Isabel,Fernandez, Franco,Mera, Xerardo Garcia,Lopez, Carmen,Rodriguez-Borges, Jose Enrique
scheme or table, p. 3426 - 3432 (2009/09/25)
In order to identify a high-affinity, selective antagonist for the A2B subtype adenosine receptor, more than 40 1,8-disubstituted-3-(3-methoxypropyl) xanthines were prepared and evaluated for their binding affinity at recombinant human adenosin
6-anilinouracil-based inhibitors of bacillus subtilis DNA polymerase III: Antipolymerase and antimicrobial structure-activity relationships based on substitution at uracil N3
Tarantino Jr., Paul M.,Zhi, Chengxin,Gambino, Joseph J.,Wright, George E.,Brown, Neal C.
, p. 2035 - 2040 (2007/10/03)
6-Anilinouracils (6-AUs) are dGTP analogues which selectively inhibit the DNA polymerase III of Bacillus subtilis and other Gram-positive bacteria. To enhance the potential of the 6-AUs as antimicrobial agents, a structure- activity relationship was devel
Fungicidal alkoxy substituted 2-cyanoacetamide derivatives
-
, (2008/06/13)
Compounds of the formula EQU1 where R is CH3 OCH2 -- or CH3 O(CH2)3 -- and R1 is alkyl of 1 or 2 carbon atoms are effective plant disease control agents.