77585-89-8 Usage
Urea derivative
A compound derived from urea (a molecule containing carbonyl groups and amino groups) Indicates the presence of a urea group in the structure, which contributes to its chemical properties.
Phenylurea family
A group of compounds that includes 1-methyl-3-(4-nitrophenyl)-1-phenylurea Classifies the compound within a specific chemical family, sharing similar properties and structures.
Pesticide and herbicide
Used in agricultural applications to control weeds Describes the primary function of the compound in agriculture, helping to manage unwanted plant growth.
Inhibitor of photosynthesis
Effectively disrupts the process of photosynthesis in plants Explains the mechanism by which the compound controls weeds, as it prevents plants from producing energy through photosynthesis.
Potential antitumor agent
Studied for its possible use in cancer treatment Suggests that the compound may have medical applications beyond its agricultural use.
Toxicity
Potentially harmful to humans and the environment Highlights the need for caution when handling the compound, as it can cause adverse effects.
Environmental impact
May have negative effects on ecosystems Points to the importance of considering the ecological consequences of using this chemical in agricultural settings.
Check Digit Verification of cas no
The CAS Registry Mumber 77585-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,8 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77585-89:
(7*7)+(6*7)+(5*5)+(4*8)+(3*5)+(2*8)+(1*9)=188
188 % 10 = 8
So 77585-89-8 is a valid CAS Registry Number.
77585-89-8Relevant articles and documents
One-pot synthesis of trisubstituted ureas from achloroaldoxime O-methanesulfonates and secondary amines
Kaeobamrung, Juthanat,Lanui, Asan,Mahawong, Sirinad,Duangmak, Witthawin,Rukachaisirikul, Vatcharin
, p. 58587 - 58594 (2018/02/19)
Trisubstituted ureas can be synthesized in a one-pot fashion from bench-stable a-chloroaldoxime Omethanesulfonates and secondary amines under mild reaction conditions. Two practical protocols have been developed to achieve various urea syntheses from both secondary aromatic amines and aliphatic amines.
