21339-73-1 Usage
Uses
Used in Pharmaceutical Industry:
2,5-Dimethyl-4-aminobenzoic acid is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Its presence in the molecular structure of these compounds contributes to their therapeutic effects and medicinal properties.
Used in Dye and Pigment Industry:
2,5-Dimethyl-4-aminobenzoic acid is utilized in the manufacturing of dyes, pigments, and UV absorbers. Its chemical structure allows it to impart color and protect materials from the damaging effects of ultraviolet radiation.
Safety Precautions:
2,5-Dimethyl-4-aminobenzoic acid is considered to be moderately hazardous, with potential health effects including skin and eye irritation. It should be handled and stored with proper precaution to minimize exposure and ensure the safety of individuals working with 2,5-DiMethyl-4-aMinobenzoic acid.
Check Digit Verification of cas no
The CAS Registry Mumber 21339-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,3 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21339-73:
(7*2)+(6*1)+(5*3)+(4*3)+(3*9)+(2*7)+(1*3)=91
91 % 10 = 1
So 21339-73-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c1-5-4-8(10)6(2)3-7(5)9(11)12/h3-4H,10H2,1-2H3,(H,11,12)
21339-73-1Relevant academic research and scientific papers
FUNGICIDAL ARYL AMIDINES
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, (2020/12/07)
This disclosure relates to aryl amidines of Formula I and their use as fungicides. One embodiment of the present disclosure is a use of a compound of Formula I, for protection of a plant against attack by a phytopathogenic organism or the treatment of a plant infested by a phytopathogenic organism, comprising the application of a compound of Formula I, or a composition comprising the compound to soil, a plant, a part of a plant, foliage, and/or roots.
Quinoline Acids
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Page/Page column 24, (2009/04/24)
This invention relates generally to quinoline-based modulators of Liver X receptors (LXRs) and related methods.
