159589-70-5 Usage
Uses
Used in Pharmaceutical Research and Development:
2-(4-METHYL-PIPERAZIN-1-YL)-BENZOIC ACID is used as a potential drug candidate for its ability to modulate various biological processes, making it a valuable asset in the development of new therapeutic agents.
Used in Cancer Treatment:
In the field of oncology, 2-(4-METHYL-PIPERAZIN-1-YL)-BENZOIC ACID is used as a therapeutic agent for its potential effects in treating various types of cancer, given its capacity to interact with biological targets involved in cancer progression.
Used in Inflammatory Disorders Treatment:
2-(4-METHYL-PIPERAZIN-1-YL)-BENZOIC ACID is utilized as a treatment option for inflammatory disorders, leveraging its potential to modulate biological pathways that contribute to inflammation.
Used as a Ligand in Drug Discovery:
In the realm of drug discovery, 2-(4-METHYL-PIPERAZIN-1-YL)-BENZOIC ACID is used as a ligand for various biological targets, such as receptors and enzymes, facilitating the identification and development of new drugs with specific actions on these targets.
Check Digit Verification of cas no
The CAS Registry Mumber 159589-70-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,5,8 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 159589-70:
(8*1)+(7*5)+(6*9)+(5*5)+(4*8)+(3*9)+(2*7)+(1*0)=195
195 % 10 = 5
So 159589-70-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2O2/c1-13-6-8-14(9-7-13)11-5-3-2-4-10(11)12(15)16/h2-5H,6-9H2,1H3,(H,15,16)
159589-70-5Relevant articles and documents
METHOD FOR PREPARING CHEMICAL COMPOUNDS OF INTEREST BY NUCLEOPHILIC AROMATIC SUBSTITUTION OF AROMATIC CARBOXYLIC ACID DERIVATIVES SUPPORTING AT LEAST ONE ELECTRO-ATTRACTIVE GROUP
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Page/Page column 12-13, (2013/02/27)
Method for preparing carboxylic acid derivatives by aromatic nucleophilic substitution, in which a carboxylic acid derivative having a single carboxyl functional group, or one of the salts thereof, the carboxylic acid derivative having, in the ortho posit
Synthesis of N-aryl and N-alkyl anthranilic acids via SNAr reaction of unprotected 2-fluoro- and 2-methoxybenzoic acids by lithioamides
Belaud-Rotureau, Mickael,Le, Tin Thanh,Phan, Thi Huong Thu,Nguyen, Thi Huu,Aissaoui, Regadia,Gohier, Frederic,Derdour, Aicha,Nourry, Arnaud,Castanet, Anne-Sophie,Nguyen, Kim Phi Phung,Mortier, Jacques
supporting information; experimental part, p. 2406 - 2409 (2010/07/17)
Substitution of the fluoro or methoxy group in unprotected 2-fluoro- and 2-methoxybenzoic acids to afford N-aryl and N-alkyl anthranilic acids occurs upon reaction with lithioamides under mild conditions in the absence of a metal catalyst.
