89837-93-4 Usage
Nitrosourea derivative
1-Nitroso-1-(2-oxopropyl)urea belongs to the class of nitrosourea compounds, which are known for their biological activity.
Application in research
1-nitroso-1-(2-oxopropyl)urea is commonly used in the study of nitrosation reactions and their potential biological effects, helping scientists understand the mechanisms and implications of these reactions.
Antitumor activity
1-Nitroso-1-(2-oxopropyl)urea has been shown to exhibit antitumor activity, making it a potential candidate for cancer treatment.
Potential anti-cancer drug
Due to its antitumor properties, 1-nitroso-1-(2-oxopropyl)urea has been investigated as a possible anti-cancer drug, with the aim of developing new and effective cancer therapies.
Mutagenic effects
1-Nitroso-1-(2-oxopropyl)urea has been found to have mutagenic effects, which means it can cause changes in the genetic material of cells.
Genotoxic effects
In addition to mutagenicity, 1-nitroso-1-(2-oxopropyl)urea also has genotoxic effects, which can lead to damage in the genetic material and potentially cause mutations or other adverse effects on the genome.
Potential environmental pollutant
Due to its mutagenic and genotoxic properties, 1-nitroso-1-(2-oxopropyl)urea is considered a potential environmental pollutant, posing risks to both human health and the environment.
Handling and disposal precautions
It is crucial to handle and dispose of 1-nitroso-1-(2-oxopropyl)urea with caution, as it may pose health and environmental hazards if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 89837-93-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,3 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89837-93:
(7*8)+(6*9)+(5*8)+(4*3)+(3*7)+(2*9)+(1*3)=204
204 % 10 = 4
So 89837-93-4 is a valid CAS Registry Number.
89837-93-4Relevant academic research and scientific papers
OXIDATION OF β-HYDROXYNITROSAMINES AND β-HYDROXYNITROSOUREAS TO THE CORRESPONDING β-OXO DERIVATIVES WITH CrO3/CELITE OR CrO3/FLORISIL IN NON-AQUEOUS MEDIA
Saavedra, Joseph E.,Farnsworth, David W.,Pei, Guo-Kui
, p. 313 - 322 (2007/10/02)
The oxidation of β-hydroxynitrosamines and β-hydroxynitrosoureas in ethyl acetate with chromic anhydride suspended in Celite or Florisil is reported.The reaction proceeded within 5-25 min, the yields were generally high, and the work-up procedure simple.T
