325796-34-7 Usage
Uses
Used in Pharmaceutical Synthesis:
4-(4-N-Benzylpiperazinyl)benzyl alcohol is used as a precursor in the pharmaceutical industry for the synthesis of various drugs. Its chemical structure makes it a valuable component in the development of new medications.
Used in Research Chemicals:
In the field of scientific research, 4-(4-N-Benzylpiperazinyl)benzyl alcohol is utilized as a starting material for the production of research chemicals, contributing to the advancement of chemical and medical research.
Used in Medical Treatments:
4-(4-N-Benzylpiperazinyl)benzyl alcohol is studied for its potential therapeutic effects in treating medical conditions such as anxiety and depression, indicating its use as a pharmaceutical agent for mental health applications.
Used in Biochemical Pathway Modulation:
4-(4-N-BENZYLPIPERAZINYL)BENZYL ALCOHOL is also being investigated for its role in modulating certain biochemical pathways within the human body, suggesting a potential use in the development of treatments that target specific biological processes.
Used in Chemical Building Blocks:
Due to its versatile chemical structure, 4-(4-N-Benzylpiperazinyl)benzyl alcohol serves as a building block in the synthesis of other chemicals, playing a crucial role in the creation of a wide range of chemical products across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 325796-34-7 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 325796-34:
(8*3)+(7*2)+(6*5)+(5*7)+(4*9)+(3*6)+(2*3)+(1*4)=167
167 % 10 = 7
So 325796-34-7 is a valid CAS Registry Number.
325796-34-7Relevant academic research and scientific papers
Antibacterial agents
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Page column 57-58, (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.
