15323-69-0 Usage
Uses
Used in Organic Synthesis:
(4-METHYL-FURAZAN-3-YL)-ACETIC ACID is used as a building block in organic synthesis for its ability to participate in a variety of chemical reactions, contributing to the formation of more complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4-METHYL-FURAZAN-3-YL)-ACETIC ACID is utilized as a precursor for the synthesis of pharmaceutical drugs, leveraging its structural and functional attributes to develop new therapeutic agents.
Used in the Development of Agrochemicals:
(4-METHYL-FURAZAN-3-YL)-ACETIC ACID is also employed in the development of agrochemicals, where its chemical properties can be harnessed to create compounds with potential applications in agriculture.
Used in the Creation of Specialized Chemicals:
Furthermore, (4-METHYL-FURAZAN-3-YL)-ACETIC ACID finds use in the production of specialized chemicals, where its versatility and reactivity are key to achieving desired outcomes in chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 15323-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,2 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15323-69:
(7*1)+(6*5)+(5*3)+(4*2)+(3*3)+(2*6)+(1*9)=90
90 % 10 = 0
So 15323-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2O3/c1-3-4(2-5(8)9)7-10-6-3/h2H2,1H3,(H,8,9)
15323-69-0Relevant academic research and scientific papers
Acid-base properties of 1,2,5-oxadiazoles. III. Furazanylacetic acids
Tselinskii,Mel'nikova,Zelenov
, p. 734 - 737 (2007/10/03)
Synthesis of 5 representatives of 4-R-furazan-3-acetic acids (R = H, CH3, NH2, NO2, N3) and 4,4′-azo- and 4,4′-azoxyfurazan-3-acetic acids is described. The pKa constants of some 4-R-furazan-3-acetic acids are determined using potentiometric titration, and inductive Taft constants of 4-substituted furanazyl groups are evaluated. The furazan ring is shown to possess a weak negative inductive effect and low conduction of polar effect of a substituent.
