342405-34-9

Basic information

• Product Name: [4-(4-METHYLPIPERAZINO)PHENYL]METHANOL
• Synonyms: [4-(4-METHYLPIPERAZINO)PHENYL]METHANOL;[4-(4-METHYLPIPERAZIN-1-YL)PHENYL]METHANOL;4-(4-METHYLPIPERAZINO)BENZYL ALCOHOL;BUTTPARK 98\50-53;RARECHEM AL BD 1090;4-(4-N-Methylpiperazinyl)benzyl alcohol;4-(4-Methylpiperazin-1-yl)benzyl alcohol
• CAS NO: 342405-34-9
• Molecular Formula: C₁₂H₁₈N₂O
• Molecular Weight: 206.28
• Product Categories: Alcohols and Derivatives;Heterocycles
• Mol File: 342405-34-9.mol
• Article Data: 4

Chemical Properties

• Melting Point: 118-120°C
• Boiling Point: 363.7 °C at 760 mmHg
• Flash Point: 189.4 °C
• Appearance: /
• Density: 1.105 g/cm³
• Vapor Pressure: 6.29E-06mmHg at 25°C
• Storage Temp.: 2-8°C
• PKA: 15.05±0.10(Predicted)
• CAS DataBase Reference: [4-(4-METHYLPIPERAZINO)PHENYL]METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: [4-(4-METHYLPIPERAZINO)PHENYL]METHANOL(342405-34-9)
• EPA Substance Registry System: [4-(4-METHYLPIPERAZINO)PHENYL]METHANOL(342405-34-9)

Safety Data

• Hazard Codes: Xi
• Statements: 34-36/37/38
• Safety Statements: 26-36/37/39
• RIDADR: 1759
• HazardClass: IRRITANT
• Hazardous Substances Data: 342405-34-9(Hazardous Substances Data)

Usage

General Description

"[4-(4-Methylpiperazino)phenyl]methanol is a chemical compound with the molecular formula C12H18N2O. It belongs to the organic compound classes of Benzene and Substituted Derivatives. It is made up of a phenol group attached to a methylpiperazine ring, which is a common moiety in a variety of pharmaceuticals and biological agents. [4-(4-METHYLPIPERAZINO)PHENYL]METHANOL is generally utilized as an intermediate in the synthesis of other chemical compounds and comes as a lightweight, volatile, colorless liquid or solid in its pure form. Its precise physical characteristics, toxicology, and potential uses are dependent on the specific conditions under which it is synthesized and processed. Overall, the compound is a significant part of many chemical and biological reactions and has various applications in scientific research and industries.

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

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

Downstream Products

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

Relevant articles and documents

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.

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