142940-79-2 Usage
Uses
Used in Organic Synthesis:
Urea, [2-(1,1-dimethylethyl)phenyl]is utilized as a reagent in organic synthesis for creating a variety of chemical compounds. Its unique structure allows it to participate in numerous chemical reactions, facilitating the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Urea, [2-(1,1-dimethylethyl)phenyl]serves as an important intermediate in the development of new drugs. Its ability to react with other molecules makes it a valuable component in medicinal chemistry, potentially leading to the discovery of novel therapeutic agents.
Used in Agriculture:
Although not explicitly detailed in the provided materials, Urea, [2-(1,1-dimethylethyl)phenyl]may find applications in agriculture, possibly as a component in the development of new agrochemicals or as a means to enhance crop protection and yield.
Used in Cosmetics:
Similarly, in the cosmetics industry, Urea, [2-(1,1-dimethylethyl)phenyl]- might be employed for its potential properties that could be beneficial in the formulation of cosmetic products, such as improving texture, stability, or providing specific功效.
Used in Manufacturing:
Urea, [2-(1,1-dimethylethyl)phenyl]may also be integrated into manufacturing processes, where its chemical properties could be harnessed to produce materials with desired characteristics for various applications, including but not limited to coatings, adhesives, or polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 142940-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,9,4 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 142940-79:
(8*1)+(7*4)+(6*2)+(5*9)+(4*4)+(3*0)+(2*7)+(1*9)=132
132 % 10 = 2
So 142940-79-2 is a valid CAS Registry Number.
142940-79-2Relevant academic research and scientific papers
Ohno, Atsuyoshi,Kunitomo, Jun,Kawai, Yasushi
, p. 4601 - 4610 (1997)
Optically active 5-deazaflavin derivatives with an axial chirality at the N(3) position have been synthesized. Kinetics for thermal enantiomerization and X-ray crystallographic analyses of these compounds have been carried out. In addition, all absolute configurations of their enantiomers have been determined on the basis of circular dichroism spectra.
