32018-86-3 Usage
Description
3-Amino-1-naphthoic acid is an organic compound that serves as a key intermediate in the synthesis of various chemical products, including herbicide antidotes. It is characterized by the presence of an amino group attached to a naphthalene ring, with a carboxylic acid group at the 1-position. This unique structure endows it with versatile reactivity and potential applications in different industries.
Uses
Used in Pharmaceutical Industry:
3-Amino-1-naphthoic acid is used as a synthesis intermediate for the development of herbicide antidotes. It plays a crucial role in the production of compounds that can counteract the effects of herbicides, which are chemicals used to control, kill, or mitigate unwanted plant growth in various settings.
Used in Chemical Synthesis:
3-Amino-1-naphthoic acid is also utilized as a versatile intermediate in the synthesis of other organic compounds. Its reactivity and functional groups make it a valuable building block for creating a wide range of chemical products, including pharmaceuticals, dyes, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 32018-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,0,1 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32018-86:
(7*3)+(6*2)+(5*0)+(4*1)+(3*8)+(2*8)+(1*6)=83
83 % 10 = 3
So 32018-86-3 is a valid CAS Registry Number.
32018-86-3Relevant articles and documents
Thrombopoietin mimetics
-
, (2008/06/13)
Non-peptide TPO mimetics are disclosed, as well as a method of treating thrombocytopenia, in a mammal, including a human, in need thereof, which comprises administering to such mammal an effective amount of a selected hydroxy-1-azo-naphthalene derivative.
Dissociation of naphthoic acids in non-aqueous media. Comparison of benzene and naphthalene skeletons
Parik, Patrik,Wolfova, Jitka,Ludwig, Miroslav
, p. 385 - 394 (2007/10/03)
Seven monosubstituted 1-naphthoic acids were synthesized by new or modified procedures, and their dissociation constants were measured potentiometrically at 25 °C in methanol, acetonitrile, dimethylformamide, and pyridine. Dissociation constants of these along with thirteen substituted 1-naphthoic acids and twenty-five substituted 2-naphthoic acids previously studied were measured at 25 °C in ethanol and dimethyl sulfoxide. The pKHA values of 3-and 4-substituted 1-naphthoic acids were treated by simple linear regression and principal component analysis, and the results were used for comparison of model compounds and of corresponding 3-and 4-substituted benzoic acids with the aim of comparison of benzene and naphthalene skeletons. It has been found, the 3 and 4 positions of the 1-naphthyl system can roughly be compared with the meta and para positions of benzene, respectively.
