20776-52-7 Usage
General Description
2-amino-6-iodobenzoic acid is a chemical compound that falls under the category of organohalogens and more specifically, iodobenzenes. It has an aromatic benzoic acid group which is substituted with an amino group at the 2nd position and an iodide at the 6th position. Its molecular formula is C7H6INO2 and has a molar mass of 285.03 g/mol. Though chemicals in its category typically possess diverse biological activities and are often used in medicinal chemistry, the specific uses and properties of 2-amino-6-iodobenzoic acid are not widely documented in literature. However, potential uses could involve creating other chemical compounds in various chemical reactions due to its functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 20776-52-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,7 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20776-52:
(7*2)+(6*0)+(5*7)+(4*7)+(3*6)+(2*5)+(1*2)=107
107 % 10 = 7
So 20776-52-7 is a valid CAS Registry Number.
InChI:InChI:1S/C7H6INO2/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3H,9H2,(H,10,11)
20776-52-7Relevant articles and documents
Chemometric analysis of substituent effects. XI. Solvent effects on dissociation of 2,6-disubstituted benzoic acids
Kulhanek, Jiri,Pytela, Oldrich
, p. 913 - 924 (1997)
Eleven symmetrically 2,6-disubstituted benzoic acids (with the following substituents: OCH3, OC2H5, OC3H7, OCH(CH3)2, OC4H9, CH3, F, Cl, Br, I, a
Nickel Boride Reduction of Aryl Nitro Compounds
Seltzman, Herbert H.,Berrang, Bertold D.
, p. 3083 - 3086 (2007/10/02)
Nickel boride smoothly reduces aryl nitro compounds to the corresponding anilines in the presence of iodo and ortho carboalkoxy groups in contrast to the problematic reductions by other methods.
