61852-05-9 Usage
Uses
Used in Organic Synthesis:
[(E)-(4-methoxyphenyl)methylidene]cyanamide is used as an intermediate in the synthesis of various organic compounds, contributing to the development of new molecules with potential applications in different industries.
Used in Chemical Research:
[(E)-(4-methoxyphenyl)methylidene]cyanamide serves as a valuable research tool for understanding the properties and reactivity of imine derivatives, which can lead to advancements in chemical science and technology.
Used in Pharmaceuticals:
[(E)-(4-methoxyphenyl)methylidene]cyanamide has been studied for its potential applications in the pharmaceutical industry, where it may contribute to the development of new drugs or drug candidates.
Used in Agrochemicals:
[(E)-(4-methoxyphenyl)methylidene]cyanamide also holds promise in the agrochemical sector, where it could be employed in the development of novel pesticides, herbicides, or other agricultural chemicals to improve crop protection and yield.
Safety Precautions:
It is crucial to handle [(E)-(4-methoxyphenyl)methylidene]cyanamide with care, as it may pose risks if ingested, inhaled, or comes into contact with the skin. Proper safety measures should be taken to minimize potential hazards during its use in research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 61852-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,5 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61852-05:
(7*6)+(6*1)+(5*8)+(4*5)+(3*2)+(2*0)+(1*5)=119
119 % 10 = 9
So 61852-05-9 is a valid CAS Registry Number.
61852-05-9Relevant academic research and scientific papers
Enantioselective reaction of N-cyano imines: decarboxylative Mannich-type reaction with malonic acid half thioesters
Inaba, Kazuto,Nakamura, Shuichi,Oyamada, Yusuke,Sasamori, Takahiro
supporting information, p. 2172 - 2175 (2022/02/17)
The enantioselective reaction of imines bearing a cyano group as an activating group with malonic acid half thioesters gave chiral cyanamide derivatives with high enantioselectivity. The density functional theory (DFT) calculation clarified the stereochemical outcome and importance of the N-cyano group for imines.
