2300-16-5 Usage
Uses
Used in Chemical Synthesis:
3,6-dinitrophthalic acid is used as a building block for the synthesis of dyes, pigments, and polymers. Its chemical structure allows it to be a versatile component in the creation of a wide range of organic compounds, contributing to the diversity of products in the chemical industry.
Used in Oil and Gas Industry:
In the oil and gas industry, 3,6-dinitrophthalic acid is utilized as a corrosion inhibitor. Its application helps to protect equipment and infrastructure from the damaging effects of corrosion, thereby enhancing the longevity and reliability of the industry's assets.
Used in Analytical Chemistry:
3,6-dinitrophthalic acid serves as a reagent in the analysis of amino acids and proteins. Its properties make it a valuable tool for researchers and scientists working in the field of biochemistry, enabling them to study and understand the structure and function of these essential biomolecules.
Check Digit Verification of cas no
The CAS Registry Mumber 2300-16-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,0 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2300-16:
(6*2)+(5*3)+(4*0)+(3*0)+(2*1)+(1*6)=35
35 % 10 = 5
So 2300-16-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H4N2O8/c11-7(12)5-3(9(15)16)1-2-4(10(17)18)6(5)8(13)14/h1-2H,(H,11,12)(H,13,14)
2300-16-5Relevant academic research and scientific papers
Overcoming regioselectivity issues inherent in bis-Troeger's base preparation
Havlik, Martin,Kral, Vladimir,Dolensky, Bohumil
, p. 4867 - 4870 (2007/10/03)
(Figure Presented) Bis-Troeger's base derivatives are a new family of molecular tweezers. A major drawback to their study is a lack of commercially available precursors, ortho-nitrocarboxylic acids. A reverse synthetic strategy starting from known dinitrodicarboxylic acids, which circumvents this problem, is presented. Via this methodology regioisomeric bis-TB derivatives can be prepared selectively, using only common aromatic amines that are typically commercially available.
