94038-26-3 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
4-(4-Benzyl-piperazin-1-yl)-benzoic acid is used as a research tool for the development of new pharmaceuticals, specifically targeting central nervous system disorders. Its unique molecular structure allows it to interact with various biological targets, making it a promising candidate for the treatment of mood disorders and other neurological conditions.
Used in the Study of Central Nervous System Disorders:
In the field of neuroscience, 4-(4-Benzyl-piperazin-1-yl)-benzoic acid is employed as a compound of interest for understanding and potentially treating a range of neurological conditions. Its interaction with the central nervous system provides insights into the mechanisms underlying these disorders and aids in the development of targeted therapies.
Used in the Treatment of Mood Disorders:
4-(4-Benzyl-piperazin-1-yl)-benzoic acid is used as a potential therapeutic agent for mood disorders. Its ability to modulate neurotransmitter systems and influence the central nervous system makes it a candidate for the development of treatments aimed at alleviating the symptoms of such conditions.
Used in the Development of Neurological Condition Treatments:
In the realm of neurology, 4-(4-Benzyl-piperazin-1-yl)-benzoic acid is utilized in the research and development of treatments for various neurological conditions. Its potential to target specific pathways and receptors within the nervous system positions it as a valuable component in the creation of new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 94038-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,3 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 94038-26:
(7*9)+(6*4)+(5*0)+(4*3)+(3*8)+(2*2)+(1*6)=133
133 % 10 = 3
So 94038-26-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H20N2O2/c21-18(22)16-6-8-17(9-7-16)20-12-10-19(11-13-20)14-15-4-2-1-3-5-15/h1-9H,10-14H2,(H,21,22)
94038-26-3Relevant articles and documents
Base-Mediated Oxidative Degradation of Secondary Amides Derived from p-Amino Phenol to Primary Amides in Drug Molecules
Nanda, Kausik K.,Ginnetti, Anthony,Wuelfing, W. Peter
, p. 3394 - 3403 (2020/08/19)
One of the most common functional groups encountered in drug molecules is the amide, and the most common degradation pathway for amides is base-mediated hydrolysis to its constituent amine and carboxylic acid. Herein, we report for the first time, a base-
Benzamide nitriles
-
Page 34, (2010/02/09)
Compounds of the formula (I) wherein m, n, A, R1, R2, R3, R4, R5 and R6 are as described herein, together with methods for making the compounds and using the compounds for treatment of diseases or conditions mediated by Cathepsin K.
Substituted chroman derivatives
-
, (2008/06/13)
The present invention relates to new new piperidyl or piperazinyl-substituted dihydro-2H-1-benzopyran derivatives compound having the formula (I) wherein X is N or CH; Y is NR2CH2, CH2NR2, NR2CO, CONR
Substituted 1,2,3,4-tetrahydronaphthalene derivatives
-
, (2008/06/13)
PCT No. PCT/SE97/00469 Sec. 371 Date Apr. 25, 1997 Sec. 102(e) Date Apr. 25, 1997 PCT Filed Mar. 20, 1997 PCT Pub. No. WO97/34883 PCT Pub. Date Sep. 25, 1997New piperidinyl- or piperazinyl-substituted-1,2,3,4-tetrahydronaphthalene derivatives having the formula wherein X is N or CH; Y is NR2CH2, CH2-NR2, NR2-CO, CO-NR2 or NR2SO2; R1is H, C1-C6 alkyl or C3-C6 cycloalkyl; R3 is C1-C6 alkyl, C3-C6 cycloalkyl or (CH2)n-aryl, where aryl is phenyl or a heteroaromatic ring containing one or two heteroatoms selected from N, O and S and which may be mono- or di-substituted; n is 0-4; as (R)-enantiomer, (S)-enantiomer or a racemate in the form of the free base or a pharmaceutically acceptable salt or hydrate thereof; a pharmaceutical formulation containing the compounds, use of the compounds in the treatment of 5-hydroxytryptamine mediated disorders, processes for the preparation of the compounds and intermediates for the preparation of the compounds.