84029-50-5 Usage
Chemical Class
Thioacetic acids
Explanation
2-[[2-(Aminocarbonyl)-5-ethoxyphenyl]thio]acetic acid belongs to the class of thioacetic acids, which are characterized by the presence of a thiol group (-SH) attached to an acetic acid backbone.
Explanation
The compound features a thioether group in its structure, which is a sulfur-oxygen bond (-S-O-) connecting two carbon-containing groups. In this case, the thioether group is attached to a phenyl ring.
Explanation
The phenyl ring is a six-carbon aromatic ring with delocalized electrons. In 2-[[2-(aminocarbonyl)-5-ethoxyphenyl]thio]acetic acid, the phenyl ring has an ethoxy (-O-ethyl) group and an aminocarbonyl (-NH-C=O) substituent.
Explanation
The ethoxy group is attached to the 5th position of the phenyl ring, which is one of the six carbon atoms in the ring. This positioning is important for the compound's properties and potential applications.
Explanation
The aminocarbonyl group, which consists of an amide bond (-C=O) and an amine group (-NH2), is attached to the 2nd position of the phenyl ring. This functional group contributes to the compound's biological activity.
Explanation
2-[[2-(Aminocarbonyl)-5-ethoxyphenyl]thio]acetic acid exhibits anti-inflammatory and antimicrobial properties, making it a potential candidate for use in pharmaceuticals as a therapeutic agent.
Explanation
The compound may also have uses in the agricultural industry as a pesticide or herbicide, due to its ability to control or eliminate unwanted organisms.
Explanation
The unique structure and properties of 2-[[2-(aminocarbonyl)-5-ethoxyphenyl]thio]acetic acid make it an interesting target for further research and development in various fields, including chemistry, biology, and materials science.
Thioether Group
Attached to a phenyl ring
Phenyl Ring
With ethoxy and aminocarbonyl substituents
Ethoxy Substituent
At position 5 of the phenyl ring
Aminocarbonyl Substituent
At position 2 of the phenyl ring
Potential Applications
Pharmaceuticals
Potential Applications
Agriculture
Research and Development
Structure and properties
Check Digit Verification of cas no
The CAS Registry Mumber 84029-50-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,2 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 84029-50:
(7*8)+(6*4)+(5*0)+(4*2)+(3*9)+(2*5)+(1*0)=125
125 % 10 = 5
So 84029-50-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO4S/c1-2-16-7-3-4-8(11(12)15)9(5-7)17-6-10(13)14/h3-5H,2,6H2,1H3,(H2,12,15)(H,13,14)
