27430-17-7 Usage
Explanation
The molecular formula represents the number of atoms of each element present in the compound, which is 14 carbon (C), 11 hydrogen (H), 3 nitrogen (N), 3 oxygen (O), and 1 sulfur (S) atoms.
Explanation
Pyrimidine derivatives are a class of organic compounds derived from the parent heterocycle, pyrimidine, which is a six-membered ring containing four carbon and two nitrogen atoms.
Explanation
The phenyl-2-propene-1-ylidene group is an organic functional group consisting of a phenyl ring attached to a 2-propene-1-ylidene moiety, which is a vinyl group (C=C) with one hydrogen atom replaced by an additional carbon-carbon double bond.
Explanation
The compound may have biological activities, which could make it useful in pharmaceutical research and development. However, further research and testing are required to determine its specific properties and uses.
Explanation
Due to its potential biological activities, the compound may be used in the development of new drugs or therapies. However, its specific applications would need to be determined through additional research.
Explanation
To fully understand the properties, uses, and potential applications of 1,2-Dihydro-2-(thioxo)-5-(3-phenyl-2-propene-1-ylidene)pyrimidine-4,6(3H,5H)-dione, further research and testing are necessary. This may include studying its chemical reactivity, stability, and interactions with biological systems.
Type of compound
Pyrimidine derivative
Presence of thioxo group
Yes
Presence of phenyl-2-propene-1-ylidene group
Yes
Biological activities
Potential
Applications
Pharmaceutical research and development
Further research and testing
Required
Check Digit Verification of cas no
The CAS Registry Mumber 27430-17-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,4,3 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27430-17:
(7*2)+(6*7)+(5*4)+(4*3)+(3*0)+(2*1)+(1*7)=97
97 % 10 = 7
So 27430-17-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2O2S/c16-11-10(12(17)15-13(18)14-11)8-4-7-9-5-2-1-3-6-9/h1-8H,(H2,14,15,16,17,18)
27430-17-7Relevant articles and documents
A study on the physical properties of low melting mixtures and their use as catalysts/solvent in the synthesis of barbiturates
Theresa, Letcy Vincent,Avudaiappan, Govindan,Shaibuna, Machingal,Hiba, Kottayil,Sreekumar, Krishnapillai
, p. 1849 - 1860 (2021/06/17)
In recent years, deep eutectic solvents have become attractive due to their interesting characteristics such as, physicochemical properties, low cost of components, easiness to prepare, low toxicity, bio-renewability, and biodegradability. In order to make the deep eutectic mixture more cost-effective and renewable, carbohydrate derivatives were linked with deep eutectic mixtures, since, carbohydrates are the most important and widespread renewable compounds on the earth. In this work, we have used low melting mixtures comprised of carbohydrates to create the reaction media for organic transformations. The physical properties such as density, viscosity, acidity, refractive index, surface tension, solubility, glass transition temperature, thermal stability, solvent polarity, and toxicity of the mixture were studied. Low melting mixtures were used as reaction media and catalysts for the effective synthesis of Barbiturates. The reaction between aldehydes and barbituric acid/thiobarbituric acid, and the reaction between aldehydes, barbituric acid/thiobarbituric acid, and malononitrile/dimedone were performed effectively with good to excellent yields. The recyclability of the catalyst/solvent was also established.
Synthesis of barbiturate-based methionine aminopeptidase-1 inhibitors
Haldar, Manas K.,Scott, Michael D.,Sule, Nitesh,Srivastava,Mallik, Sanku
, p. 2373 - 2376 (2008/09/20)
The syntheses of a new class of barbiturate-based inhibitors for human and Escherichia Coli methionine aminopeptidase-1 (MetAP-1) are described. Some of the synthesized inhibitors show selective inhibition of the human enzyme with high potency.
