33024-79-2 Usage
Physical appearance
Colorless 1-methoxy-3-methylurea is a colorless compound, which means it does not have any visible color.
Odor
Odorless This compound has no distinct smell that can be detected by the human nose.
Solubility
Water-soluble 1-methoxy-3-methylurea can dissolve in water, making it suitable for use in various aqueous solutions and applications.
Industrial and agricultural applications
Corrosion inhibitor, stabilizer for chlorine dioxide, component in herbicides and pesticides This compound is used in a variety of applications, including preventing metal corrosion, stabilizing chlorine dioxide, and controlling weeds and pests in agriculture.
Pharmaceutical synthesis
Solvent in chemical reactions 1-methoxy-3-methylurea is used as a solvent in the synthesis of pharmaceuticals, aiding in the chemical reactions required to create various drugs.
Advanced material development
Potential application in electrochemistry and advanced materials Due to its unique chemical and physical properties, this compound has potential uses in the development of new materials and electrochemical applications.
Health hazards
Skin, eye, and respiratory system irritation It is important to handle 1-methoxy-3-methylurea with care, as it can cause irritation to the skin, eyes, and respiratory system upon exposure. Proper safety measures should be taken when working with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 33024-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,2 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33024-79:
(7*3)+(6*3)+(5*0)+(4*2)+(3*4)+(2*7)+(1*9)=82
82 % 10 = 2
So 33024-79-2 is a valid CAS Registry Number.
33024-79-2Relevant articles and documents
N,N-DIALKOXY-N'-ALKYLUREAS
Rudchenko, V. F.,Ignatov, S. M.,Kostyanovskii, R. G.
, p. 1920 - 1921 (1992)
The chlorination of N-alkoxy-N'-alkylureas (1) by the action of t-BuOCl proceeds regiospecifically to give stable N-chloro-N-alkoxy-N'-alkylureas (2).The alcoholysis of 2 leads to N,N-dialkoxy-N'-alkylureas (3).The alkaline hydrolysis of 3 is a new, convenient method for the preparation of dialkoxyamines.Keywords: N-alkoxy-N'-alkylureas, N-chloro-N-alkoxy-N'-aklylureas, N,N-dialkoxy-N'-alkylureas, dialkoxyamines.
Synthesis of potential anticancer agents. 38. N-Nitrosoureas. 4. Further synthesis and evaluation of haloethyl derivatives.
Johnston,McCaleb,Opliger,Laster,Montgomery
, p. 600 - 614 (2007/10/04)
-
