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2-(1-Piperazinyl)quinoline

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Identification
Molecular formula
C13H15N3
CAS number
1822-77-3
IUPAC name
2-piperazin-1-ylquinoline
State
State
At room temperature, 2-(1-Piperazinyl)quinoline is typically in a solid state. It remains stable under normal conditions and is used in various settings that require a solid form for mixing and reaction purposes.
Melting point (Celsius)
71.00
Melting point (Kelvin)
344.15
Boiling point (Celsius)
391.20
Boiling point (Kelvin)
664.35
General information
Molecular weight
212.28g/mol
Molar mass
212.2840g/mol
Density
1.1750g/cm3
Appearence

2-(1-Piperazinyl)quinoline appears as a crystalline solid. It is often beige to off-white in color and exhibits a powdery texture. The compound is common in research labs where its solid-state form is used for various synthetic applications.

Comment on solubility

Solubility of 2-piperazin-1-ylquinoline (C13H15N3)

Understanding the solubility characteristics of 2-piperazin-1-ylquinoline is essential for researchers and chemists alike. This compound, with its complex structure, exhibits notable solubility behavior influenced by several factors:

  • Polarity: The presence of nitrogen atoms in the piperazine ring can enhance its polarity, which may lead to increased solubility in polar solvents.
  • Hydrogen Bonding: This compound is likely to be capable of forming hydrogen bonds, further promoting its solubility in polar aprotic solvents.
  • Hydrophobic Interactions: The quinoline moiety contributes to hydrophobic characteristics, which may limit its solubility in highly polar solvents.

As a result, one can generally expect 2-piperazin-1-ylquinoline to be:

  • Moderately soluble in water due to its polar regions, but solubility may vary considerably with changes in temperature and pH.
  • More soluble in organic solvents that align better with its hydrophobic quinoline portion, such as dimethyl sulfoxide (DMSO) or ethanol.

In conclusion, the solubility of 2-piperazin-1-ylquinoline varies based on the solvent characteristics and environmental conditions. Knowledge of these properties is crucial for applications in pharmaceuticals, where solubility plays a pivotal role in drug formulation and efficacy.

Interesting facts

Interesting Facts About 2-Piperazin-1-ylquinoline

2-Piperazin-1-ylquinoline is a fascinating compound with intriguing applications and properties. Here are some noteworthy facts:

  • Structure and Functionality: This compound consists of a quinoline ring structure fused with a piperazine moiety. The presence of these two functional groups enhances its biological activity, making it an area of interest in medicinal chemistry.
  • Medicinal Potential: Compounds like 2-piperazin-1-ylquinoline are often researched for their potential in drug development. They exhibit promising activity against various biological targets, including cancer and infectious diseases.
  • Diverse Applications: Beyond its medicinal uses, this compound can also serve as a building block for synthesizing other complex molecules. Its versatility is appealing in the field of organic synthesis.
  • Pharmacological Research: Due to its structural features, this compound is of particular interest in pharmacological research for designing novel therapeutic agents that may offer improved efficacy or safety profiles.
  • Structure-Activity Relationship (SAR): Scientists study the SAR of 2-piperazin-1-ylquinoline to understand how variations in its structure can influence its biological activity, leading to more effective drug candidates.

In summary, 2-piperazin-1-ylquinoline stands out in the realm of chemical compounds, combining unique structural attributes with significant pharmacological potential. Its exploration continues to foster advancements in both medicinal chemistry and synthetic methods.

Synonyms
quipazine
2-Piperazin-1-yl-quinoline
4774-24-7
2-(piperazin-1-yl)quinoline
2-Piperazin-1-ylquinoline
2-(1-Piperazinyl)quinoline
Quipazine [INN]
Quinoline, 2-(1-piperazinyl)-
Quipazina
Quipazinum
1-(2-Quinolinyl)piperazine
Quipazinum [INN-Latin]
Quipazina [INN-Spanish]
1-(2-Quinolyl)piperazine
2-(1-Piperazinyl)chinolin
UNII-4WCY05C0SJ
4WCY05C0SJ
MFCD00242605
BRN 0196945
CHEMBL18772
DTXSID3046952
5-23-03-00069 (Beilstein Handbook Reference)
130895-61-3
Quipazinum (INN-Latin)
Quipazina (INN-Spanish)
2-(1-PIPERAZINO)QUINOLINE
Spectrum_001733
Tocris-0629
piperazin-1-yl-quinoline
Prestwick0_000617
Prestwick1_000617
Prestwick2_000617
Prestwick3_000617
Spectrum2_001182
Spectrum3_001824
Spectrum4_001259
Lopac-Q-1004
Biomol-NT_000103
Lopac0_001019
Oprea1_342540
BSPBio_000554
BSPBio_003467
GTPL173
KBioGR_001818
KBioSS_002213
1-(quinolin-2-yl)piperazine
2-(1-piperazinyl)-quinoline
DivK1c_000911
SCHEMBL322181
SPBio_001223
SPBio_002773
2-(piperazin-1-yl)-quinoline
BPBio1_000610
BPBio1_001393
F3306-0004
DTXCID1026952
CHEBI:93368
KBio1_000911
KBio2_002213
KBio2_004781
KBio2_007349
KBio3_002971
NINDS_000911
XRXDAJYKGWNHTQ-UHFFFAOYSA-N
BCP23281
BDBM50014407
STL308727
AKOS000124312
2-Piperazin-1-yl-quinoline(Quipazine)
AB05466
CCG-205099
HY-W028142
IDI1_000911
2-Piperazin-1-yl-quinoline (Quipazine)
NCGC00015872-01
NCGC00015872-02
NCGC00015872-03
NCGC00015872-04
NCGC00015872-06
NCGC00024694-01
NCGC00024694-02
NCGC00024694-03
AC-22858
AS-38262
SY238379
CAS-4774-24-7
SBI-0050992.P003
DB-021505
AB00053761
CS-0072166
EN300-39715
VU0005330-3
P67440
AB00053761-06
AB00053761_11
AB00053761_12
L000958
Q7272557
BRD-K77925998-001-01-3
BRD-K77925998-050-02-8
BRD-K77925998-050-14-3
BRD-K77925998-332-03-8
BRD-K77925998-332-04-6
BRD-K77925998-364-01-5
2-Piperazin-1-yl-quinoline;2-(piperazin-1-yl)quinoline