116465-92-0 Usage
Uses
Used in Pharmaceutical Industry:
2-Nitro-3-aminobenzoic acid is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique chemical structure allows it to undergo different chemical reactions, enabling the creation of derivatives with distinct properties and applications in the development of new medications.
Used in Dye Industry:
2-Nitro-3-aminobenzoic acid is also used in the synthesis of dyes. Its ability to form various derivatives through chemical reactions makes it a valuable component in the production of a wide range of dyes with different color characteristics and properties.
Used in Organic Synthesis:
As a building block in organic synthesis, 2-Nitro-3-aminobenzoic acid is utilized in the creation of complex organic compounds. Its versatile chemical properties make it an essential component in the synthesis of various organic compounds for research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 116465-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,6 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 116465-92:
(8*1)+(7*1)+(6*6)+(5*4)+(4*6)+(3*5)+(2*9)+(1*2)=130
130 % 10 = 0
So 116465-92-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O4/c8-5-3-1-2-4(7(10)11)6(5)9(12)13/h1-3H,8H2,(H,10,11)
116465-92-0Relevant articles and documents
A convenient copper-catalyzed direct animation of nitroarenes with 9-alkylhydroxylamines
Seko, Shinzo,Miyake, Kunihito,Kavvamura, Norio
, p. 1437 - 1444 (2007/10/03)
O-Alkylhydroxylamines, particularly O-methylhydroxylamine, aminate nitroarenes in the presence of a strong base and a copper catalyst to give aminonitroarenes in good yields, ortho- or para-Animation with respect to the nitro group takes place, and in some cases the ortho-aminated product is preferentially obtained. With 3-substituted nitrobenzenes where the substituent has a lone pair of electrons, preferential amination occurs at the 2-position to give the sterically most congested 3c-f, 14 and 22g.