115651-29-1 Usage
Uses
Used in Pharmaceutical Industry:
5-ACETYL-2-AMINO-4-HYDROXYBENZOIC ACID is used as an intermediate in organic synthesis for the development of new pharmaceuticals, leveraging its anti-inflammatory and anti-cancer properties to address various health conditions.
Used in Anti-inflammatory Applications:
5-ACETYL-2-AMINO-4-HYDROXYBENZOIC ACID is employed as an anti-inflammatory agent, potentially mitigating inflammation and associated symptoms by modulating the body's immune response.
Used in Anti-cancer Applications:
5-ACETYL-2-AMINO-4-HYDROXYBENZOIC ACID is utilized as an anti-cancer agent, targeting the inhibition of dihydrofolate reductase, which is essential for cancer cell proliferation, thereby disrupting the synthesis of DNA and RNA in cancer cells and potentially limiting tumor growth.
Used in Antimicrobial Applications:
5-ACETYL-2-AMINO-4-HYDROXYBENZOIC ACID is used as an antimicrobial agent for treating bacterial and fungal infections, demonstrating its potential to combat a range of infectious diseases by inhibiting the growth of pathogenic microorganisms.
Check Digit Verification of cas no
The CAS Registry Mumber 115651-29-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,6,5 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 115651-29:
(8*1)+(7*1)+(6*5)+(5*6)+(4*5)+(3*1)+(2*2)+(1*9)=111
111 % 10 = 1
So 115651-29-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO4/c1-4(11)5-2-6(9(13)14)7(10)3-8(5)12/h2-3,12H,10H2,1H3,(H,13,14)/p-1
115651-29-1Relevant academic research and scientific papers
Synthesis of Benzoic Acid Derivatives from 3-Ethoxymethylene-2,4-alkanediones and Malononitrile
Schmidt, Hans-Werner,Kores, Margarete
, p. 1001 - 1004 (2007/10/02)
Reaction of the 3-ethoxymethylene-2,4-alkanediones 1a-c with malononitrile (2) gives the benzonitrile derivatives 3a-c.Compounds 4a-d are obtained by acid or basic hydrolysis of the nitrile group of 3a-c, Sandmeyer reaction leads to the halogenated benzonitriles 5a-f.Compounds 6a,b are available from 3a and O-ethyl- and O-allylhydroxylamine hydrochloride.
