23050-91-1 Usage
Uses
Used in Pharmaceutical Synthesis:
4-DIMETHYLAMINOSALICYLIC ACID is used as a precursor in the synthesis of various pharmaceuticals, leveraging its chemical properties to contribute to the development of new medicinal compounds.
Used in Dye Production:
4-DIMETHYLAMINOSALICYLIC ACID is also utilized in the production of dyes, where its chemical structure imparts color and stability to the final products.
Used in Analytical Chemistry:
4-DIMETHYLAMINOSALICYLIC ACID is used as a reagent for the determination of certain metals, such as copper and nickel, due to its ability to form chelates with these metal ions.
Used in Medicine and Biochemistry:
Due to its biological activity and metal-chelating properties, 4-DIMETHYLAMINOSALICYLIC ACID has potential applications in medicine and biochemistry, where it may be employed in the development of treatments or diagnostic tools.
Check Digit Verification of cas no
The CAS Registry Mumber 23050-91-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,5 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23050-91:
(7*2)+(6*3)+(5*0)+(4*5)+(3*0)+(2*9)+(1*1)=71
71 % 10 = 1
So 23050-91-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO3/c1-10(2)6-3-4-7(9(12)13)8(11)5-6/h3-5,11H,1-2H3,(H,12,13)
23050-91-1Relevant academic research and scientific papers
Carboxylation of Phenols with CO2 at Atmospheric Pressure
Luo, Junfei,Preciado, Sara,Xie, Pan,Larrosa, Igor
supporting information, p. 6798 - 6802 (2016/05/11)
A convenient and efficient method for the ortho-carboxylation of phenols under atmospheric CO2 pressure has been developed. This method provides an alternative to the previously reported Kolbe-Schmitt method, which requires very high pressures of CO2. The addition of a trisubstituted phenol has proved essential for the successful carboxylation of phenols with CO2 at standard atmospheric pressure, allowing the efficient preparation of a broad variety of salicylic acids.
