5443-80-1 Usage
Uses
Used in Pharmaceutical Industry:
5-bromo-4-[(1-cyclohexyl-2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)methyl]-2-methoxyphenoxyacetic acid is used as a potential pharmaceutical compound for its diverse chemical and biological properties. The complex structure of this molecule may allow it to interact with various biological targets, making it a candidate for the development of new drugs or therapies.
Used in Chemical Research:
In the field of chemical research, 5-bromo-4-[(1-cyclohexyl-2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)methyl]-2-methoxyphenoxyacetic acid serves as a subject of study to understand its reactivity, stability, and potential applications in the synthesis of other complex organic molecules. Its unique structure may provide insights into new reaction pathways or mechanisms.
Used in Material Science:
5-bromo-4-[(1-cyclohexyl-2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)methyl]-2-methoxyphenoxyacetic acid 5-bromo-4-[(1-cyclohexyl-2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)methyl]-2-methoxyphenoxyacetic acid may also find applications in material science, where its properties can be explored for the development of new materials with specific characteristics, such as improved stability, reactivity, or selectivity in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 5443-80-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5443-80:
(6*5)+(5*4)+(4*4)+(3*3)+(2*8)+(1*0)=91
91 % 10 = 1
So 5443-80-1 is a valid CAS Registry Number.
5443-80-1Relevant academic research and scientific papers
Metal-free C–H arylation of aminoheterocycles with arylhydrazines
Taniguchi, Toshihide,Imoto, Mitsutaka,Takeda, Motonori,Matsumoto, Fukashi,Nakai, Takeo,Mihara, Masatoshi,Mizuno, Takumi,Nomoto, Akihiro,Ogawa, Akiya
, p. 4132 - 4140 (2016/07/06)
A direct C–H arylation of aminoheterocycles with arylhydrazine hydrochlorides was developed. The reaction proceeds via a homolytic aromatic substitution mechanism involving aryl radicals as the intermediates. The new reaction takes place readily at room t
Chiral phosphoric acid-catalyzed asymmetric transfer hydrogenation of quinolin-3-amines
Cai, Xian-Feng,Guo, Ran-Ning,Feng, Guang-Shou,Wu, Bo,Zhou, Yong-Gui
supporting information, p. 2680 - 2683 (2014/06/09)
A chiral phosphoric acid catalyzed asymmetric transfer hydrogenation of aromatic amines, quinolin-3-amines, was successfully developed with up to 99% ee. To supplement our previous work on the Ir-catalyzed asymmetric hydrogenation of 2-alkyl substituted q
