10414-66-1 Usage
Uses
Used in Pharmaceutical Industry:
[(4-nitrobenzoyl)oxy]acetic acid is used as a key intermediate in the synthesis of pharmaceuticals due to its unique reactivity and structural properties. The presence of the nitro group allows for further chemical modifications, enabling the development of a wide range of drugs with diverse therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, [(4-nitrobenzoyl)oxy]acetic acid serves as a vital building block for the creation of new chemical compounds with potential applications in agriculture. Its unique structure and reactivity contribute to the development of novel agrochemicals, such as pesticides and herbicides, that can help improve crop protection and yield.
Used in Organic Synthesis Research:
[(4-nitrobenzoyl)oxy]acetic acid is employed as a valuable precursor in organic synthesis research. Its unique structure and reactivity make it an attractive candidate for the development of new chemical compounds with potential applications in various fields, including materials science, pharmaceuticals, and agrochemicals. Researchers can exploit its properties to design and synthesize novel molecules with specific functionalities and improved performance.
Check Digit Verification of cas no
The CAS Registry Mumber 10414-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,1 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10414-66:
(7*1)+(6*0)+(5*4)+(4*1)+(3*4)+(2*6)+(1*6)=61
61 % 10 = 1
So 10414-66-1 is a valid CAS Registry Number.
10414-66-1Relevant academic research and scientific papers
Anodic Oxidation of O-Benzoylated α-Hydroxyacetic Acids - A Contribution to the Reactivity of Anodic Oxidated Carboxylate Ions - "Umpolung"
Thomas, H. Guenter,Kessel, Stephan
, p. 2777 - 2788 (2007/10/02)
Anodic oxidation of O-benzoylated α-hydroxyacetic acid 1 at graphite electrodes in methanol leads to the corresponding mixed acylals 2 and methyl benzoates 3.The rate 2:3 depends on the substitution of the aromatic ring and can be correlated to Hammett's ?-values.
