CAS 102292-50-2
:1-(2,6-DICHLOROBENZYL)PIPERAZINE
Description:
1-(2,6-Dichlorobenzyl)piperazine is a chemical compound characterized by its piperazine core, which is a six-membered ring containing two nitrogen atoms. The presence of a 2,6-dichlorobenzyl group significantly influences its chemical properties and biological activity. This compound is typically a white to off-white solid and is soluble in organic solvents, reflecting its hydrophobic characteristics due to the aromatic ring and chlorinated substituents. It is often studied for its potential pharmacological applications, particularly in the field of neuroscience, as piperazine derivatives can exhibit various effects on neurotransmitter systems. The dichlorobenzyl moiety may enhance its binding affinity to certain receptors, making it of interest in drug development. Additionally, safety and handling precautions are essential, as halogenated compounds can pose environmental and health risks. As with many chemical substances, its reactivity and stability can be influenced by factors such as temperature, pH, and the presence of other chemicals.
Formula:C11H14Cl2N2
InChI:InChI=1/C11H14Cl2N2/c12-10-2-1-3-11(13)9(10)8-15-6-4-14-5-7-15/h1-3,14H,4-8H2
SMILES:c1cc(c(CN2CCNCC2)c(c1)Cl)Cl
Synonyms:- Timtec-Bb Sbb009351
- Akos B014424
- Buttpark 36\08-57
- Art-Chem-Bb B014424
- 1-(2,6-Dichloro-Benzyl)-Pierpazine
- 1-(2,6-Dichlorobenzyl)-Piperazine >98%
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Found 2 products.
Piperazine, 1-[(2,6-dichlorophenyl)methyl]-
CAS:Formula:C11H14Cl2N2Purity:98%Color and Shape:SolidMolecular weight:245.14831-(2,6-Dichlorobenzyl)piperazine
CAS:Controlled Product<p>1-(2,6-Dichlorobenzyl)piperazine is a benzylpiperazine that emits light in the visible region. It is an acidic reagent that can be used as an electron donating agent in organic synthesis. 1-(2,6-Dichlorobenzyl)piperazine reacts with amines to form substituted phenylpiperazines. This reaction is widely used to investigate the structure and reactivity of amines. 1-(2,6-Dichlorobenzyl)piperazine reacts with phenols to form piperazines. It also reacts with aliphatic compounds to form a trifluoromethyl group.</p>Formula:C11H14Cl2N2Purity:Min. 95%Molecular weight:245.15 g/mol

