342405-34-9

Usage

Uses

Used in Pharmaceutical Industry:
[4-(4-Methylpiperazino)phenyl]methanol is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its presence in the structure of many drugs makes it an essential component in the development of new medications and therapies.
Used in Chemical Research:
In the field of chemical research, [4-(4-Methylpiperazino)phenyl]methanol is used as a reagent or starting material for the preparation of more complex molecules. Its versatility in forming different chemical structures allows researchers to explore its potential in creating novel compounds with unique properties.
Used in Biological Research:
[4-(4-Methylpiperazino)phenyl]methanol is employed as a component in the synthesis of biological agents, such as peptides, proteins, and other biomolecules. Its incorporation into these agents can lead to the discovery of new biological activities and potential therapeutic applications.
Used in Material Science:
In material science, [4-(4-Methylpiperazino)phenyl]methanol may be used as a building block for the development of new materials with specific properties, such as improved conductivity, enhanced stability, or novel optical characteristics. Its role in the synthesis of these materials contributes to advancements in various industries, including electronics, energy, and medicine.

InChI:InChI=1/C12H18N2O/c1-13-6-8-14(9-7-13)12-4-2-11(10-15)3-5-12/h2-5,15H,6-10H2,1H3/p+1

Upstream product

• 197638-83-8 4-(4-(1,1-dimethylethoxycarbonyl)piperazinyl)benzaldehyde 
• 27913-99-1 4-(4-methylpiperazin-1-yl) benzaldehyde 
• 459-57-4 4-fluorobenzaldehyde 
• 109-01-3 1-methyl-piperazine 

Downstream Products

• 27913-99-1 4-(4-methylpiperazin-1-yl) benzaldehyde 
• 1258379-39-3 C₃₈H₃₄F₁₀N₄ 
• 1258379-31-5 p-(4-methylpiperazinyl)benzyltriphenylphosphonium bromide 
• 34334-28-6 4-(4-methylpiperazin-1-yl)benzonitrile 

Relevant academic research and scientific papers

Combined KOH/BEt3Catalyst for Selective Deaminative Hydroboration of Aromatic Carboxamides for Construction of Luminophores

The selective catalytic C-N bond cleavage of amides into value-added amine products is a desirable but challenging transformation. Molecules containing iminodibenzyl motifs are prevalent in pharmaceutical molecules and functional materials. Here we established a combined KOH/BEt3 catalyst for deaminative hydroboration of acyl-iminodibenzyl derivatives, including nonheterocyclic carboxamides, to the corresponding amines. This novel transition-metal-free methodology was also applied to the construction of Clomipramine and luminophores.

TREATMENT OF DISEASES BY EPIGENETIC REGULATION

The present disclosure provides non-naturally occurring polyphenol compounds that inhibit the bromodomain and extra terminal domain (BET) proteins. The disclosed compositions and methods can be used for treatment and prevention of cancer, including NUT midline carcinoma, Burkitt's Lymphoma, Acute Myelogenous Leukemia, and Multiple Myeloma; autoimmune or inflammatory diseases or conditions, and sepsis.

Novel fluorinated amino-stilbenes and their solid-state photodimerization

We synthesized a series of polyfluoro-amino-stilbenes in satisfactory yields by Wittig reaction of 4-piperazinyl-benzalhehydes with pentafluoro-benzylidene-triphenyl-phosphorane and we analyzed the photochemical behavior of these stilbenes in the solid st

COMPOUNDS FOR THE PREVENTION AND TREATMENT OF CARDIOVASCULAR DISEASES

The present disclosure relates to compounds, which are useful for regulating the expression of apolipoprotein A-I (ApoA-I), and their use for treatment and prevention of cardiovascular disease and related disease states, including cholesterol- or lipid-related disorders, such as, for example, atherosclerosis.