325796-35-8 Usage
Uses
Used in Pharmaceutical Research and Drug Synthesis:
4-(1-Piperazinyl)benzyl alcohol is utilized as an intermediate in the synthesis of various pharmaceutical compounds due to its unique chemical structure and properties. Its presence in the benzyl alcohol and piperazine chemical classes makes it a valuable component in the development of new drugs.
Used in Organic Compound Production:
4-(1-Piperazinyl)benzyl alcohol serves as a key ingredient in the production of a range of organic compounds, contributing to the advancement of organic chemistry and the creation of novel materials and substances.
Used in Treatment of Anxiety and Mood Disorders:
4-(1-Piperazinyl)benzyl alcohol is used as a therapeutic agent for its sedative and anxiolytic properties, potentially offering relief to individuals suffering from anxiety and mood disorders. Its application in this area is still under investigation, with the aim of understanding its full therapeutic potential and safety profile.
Further research is essential to determine the optimal use of 4-(1-Piperazinyl)benzyl alcohol in these applications and to explore any additional uses that may arise from a deeper understanding of its biological activity.
Check Digit Verification of cas no
The CAS Registry Mumber 325796-35-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,5,7,9 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 325796-35:
(8*3)+(7*2)+(6*5)+(5*7)+(4*9)+(3*6)+(2*3)+(1*5)=168
168 % 10 = 8
So 325796-35-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N2O/c14-9-10-1-3-11(4-2-10)13-7-5-12-6-8-13/h1-4,12,14H,5-9H2
325796-35-8Relevant academic research and scientific papers
Antibacterial agents
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Page column 58, (2010/02/10)
Compounds of formula (II) are antibacterial agents wherein Q represents a radical of the formula: —N(OH)CH(═O) or the formula: —C(═O)NH(OH); R1 represents hydrogen, C1-C6 alkyl or C1-C6 alkyl substituted by one or more halogen atoms, or, except when Q is a radical of the formula: —N(OH)CH(═O), a hydroxy, C1-C6 alkoxy, C1-C4 alkenyloxy, amino, C1-C4 alkylamino, or di-(C1-C6 alkyl)amino group; R2 represents a substituted or unsubstituted C1-C6 alkyl, cycloalkyl(C1-C6 alkyl)- or aryl(C1-C6 alkyl)-group; and A represents a group of formula (IIA), or (IIB) wherein R4 represents the side chain of a natural or non-natural alpha amino acid, and R5 and R6 when taken together with the nitrogen atom to which they are attached form a saturated heterocyclic first ring of 5 to 7 atoms as specified in the description.
