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N'-benzyl-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine

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Identification
Molecular formula
C16H23N3
CAS number
12345-67-8
IUPAC name
N'-benzyl-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine
State
State

This compound is a liquid at room temperature, characterized by its viscous texture. It typically maintains a stable form without solidifying under normal ambient conditions.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
334.50
Boiling point (Kelvin)
607.70
General information
Molecular weight
255.37g/mol
Molar mass
255.3690g/mol
Density
1.0300g/cm3
Appearence

N'-benzyl-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine is typically a colorless to pale yellow liquid. The compound does not form crystals and appears as a viscous substance.

Comment on solubility

Solubility of N'-benzyl-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine (C16H23N3)

The solubility of N'-benzyl-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine is an interesting aspect worth noting, particularly due to its structural characteristics. This compound exhibits a unique blend of properties that influence its solubility in various solvents.

In general, the solubility factors can be summarized as follows:

  • Polarity: The presence of the pyridine ring contributes to a certain level of polarity, impacting its interaction with polar solvents.
  • Hydrophobic Interactions: The benzyl group provides a hydrophobic character, making it more soluble in nonpolar solvents.
  • Amine Functionalities: The amine groups in the structure can form hydrogen bonds, which enhance solubility in polar protic solvents.

As a result, we can say:

  1. It is likely to be more soluble in organic solvents such as ethanol, methanol, and acetone.
  2. It may have limited solubility in water, despite the presence of polar functional groups, due to conflicting hydrophobic characteristics.

In conclusion, the solubility of N'-benzyl-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine will greatly depend on the solvent environment, which can vary widely based on the specific chemical interactions taking place.

Interesting facts

Exploring N'-benzyl-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine

N'-benzyl-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine is an intriguing compound in the realm of organic chemistry. Below are some captivating aspects associated with this versatile chemical:

  • Diverse Applications: This compound is particularly noteworthy for its potential applications in medicinal chemistry. Its functional groups suggest it could act as a ligand in various biological systems, possibly enhancing pharmacological activities.
  • Pyridine Influence: The presence of the 2-pyridyl group is significant. Pyridine derivatives often exhibit interesting metabolic pathways and can help enhance solubility and bioactivity in drug design. Their ability to interact with biological targets makes them valuable for pharmaceutical research.
  • Amine Chemistry: As an amine, the compound displays basic properties, enabling it to participate in a range of organic reactions, including nucleophilic substitutions and coupling reactions. This makes it a core structure for synthesizing more complex molecules.
  • Recent Research: In recent studies, researchers have focused on similar compounds that showcase potential anti-cancer properties. The arrangement of groups in this compound may be leveraged to optimize these effects further.
  • Synergistic Effects: The combination of benzyl and dimethyl groups contributes to the compound's electronic properties. This molecular architecture could allow for synergistic interactions when combined with other agents, enhancing their efficacy in therapeutic applications.

In summary, N'-benzyl-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine is more than just a chemical; it holds a wealth of opportunity for exploration in both organic synthesis and medicinal applications, lending itself to multiple avenues of scientific inquiry and innovation.

Synonyms
tripelennamine
Pyribenzamine
91-81-6
Pyrinamine base
Tripelennamin
Benzoxale
Piribenzil
Resistamine
Cizaron
Tonaril
Tripelenamine
Tripelennamina
Pyribenzamin
Tripelenamina
Ts and Blues
Tripelannamine
Tripelennaminum
Vetibenzamina
Tripelennamine [INN]
1,2-Ethanediamine, N,N-dimethyl-N'-(phenylmethyl)-N'-2-pyridinyl-
NCI-C60662
Tripelenamina [INN-Spanish]
Tripelennaminum [INN-Latin]
Pyristine (piristina)
2-(Benzyl(2-dimethylaminoethyl)amino)pyridine
N,N-Dimethyl-N'-benzyl-N'-(2-pyridyl)ethylenediamine
NSC 118946
N-Benzyl-N-(2-pyridyl)-N',N'-dimethyl ethylenediamine
HSDB 5191
N'-benzyl-N,N-dimethyl-N'-pyridin-2-ylethane-1,2-diamine
2-(N-Benzyl-N-(2-dimethylaminoethyl)amino)pyridine
N-Benzyl-N',N'-dimethyl-N-2-pyridylethylenediamine
UNII-3C5ORO99TY
beta-Dimethylaminoethyl-2-pyridylbenzylamine
beta-Dimethylaminoethyl-2-pyridylaminotoluene
EINECS 202-100-1
3C5ORO99TY
NSC-118946
BRN 0227074
N,N-Dimethyl-N'-(phenylmethyl)-N'-2-pyridinyl-1,2-ethanediamine
Tripelennamine (INN)
N-benzyl-N-[2-(dimethylamino)ethyl]pyridin-2-amine
2750 R.P.
N-Benzyl-N',N'-dimethyl-N-(2-pyridyl)ethylenediamine
Benzyl-(alpha-pyridyl)-dimethylaethylendiamin
2-[Benzyl(2-dimethylaminoethyl)amino]pyridine
Ethylenediamine, N-benzyl-N',N'-dimethyl-N-(2-pyridyl)-
N,N-Dimethyl-N'-benzyl-N'-(alpha-pyridyl)ethylenediamine
Pyridine, 2-(benzyl(2-(dimethylamino)ethyl)amino)-
CHEBI:9741
DTXSID8023717
Benzyl-.alpha.-pyridyl-dimethyl-aethylendiamin
.beta.-Dimethylaminoethyl-2-pyridylaminotoluene
5-22-08-00378 (Beilstein Handbook Reference)
Pyridbenzamine
Tripellenamine
Triplennamine
N,N-Dimethyl-N'-benzyl-N'-(.alpha.-pyridyl)ethylenediamine
N-Benzyl-N',N'-dimethyl-N-pyridin-2-ylethane-1,2-diamine
.beta.-Dimethylaminoethyl-2-pyridylbenzylamine
N'-benzyl-N,N-dimethyl-N'-pyridin-2-ylethane-1,2-diamine;hydron;chloride
Tripelennamina [Italian]
Tripelenamina (INN-Spanish)
Tripelennaminum (INN-Latin)
2-[N-Benzyl-N-(2-dimethylaminoethyl)amino]pyridine
Pyridine, 2-[benzyl[2-(dimethylamino)ethyl]amino]-
Tripelennamine [INN:BAN]
Benzyl-(alpha-pyridyl)-dimethylaethylendiamin [German]
ReCovr (Salt/Mix)
Dehistin (Salt/Mix)
Ahistamin (Salt/Mix)
Spectrum_000141
Stanzamine (Salt/Mix)
Tri-Tumine (Salt/Mix)
Spectrum2_000957
Spectrum3_001696
Spectrum4_000374
Spectrum5_001581
TRIPELENNAMINE [MI]
2-(benzyl(2-(dimethylamino)ethyl)amino)pyridine
CHEMBL1241
Oprea1_266730
SCHEMBL17970
BSPBio_003252
KBioGR_000867
KBioSS_000621
TRIPELENNAMINE [HSDB]
DivK1c_000534
TRIPELENNAMINE [VANDF]
SPBio_000954
DTXCID803717
GTPL7318
N-Benzyl-N',N'-dimethyl-N-2-(pyridylethylene)diamine
TRIPELENNAMINE [WHO-DD]
BDBM81471
KBio1_000534
KBio2_000621
KBio2_003189
KBio2_005757
KBio3_002472
D04AA04
R06AC04
NINDS_000534
AntiAllergicum Medivet (Salt/Mix)
NSC_5587
WLN: T6NJ BN1R&2N1&1
1,2-Ethanediamine,N1,N1-dimethyl-N2-(phenylmethyl)-N2-2-pyridinyl-
HY-17428A
N,N-dimethyl-N'-(phenylmethyl)-N'-pyridin-2-ylethane-1,2-diamine
NSC118946
DB00792
FT65196
CAS_91-81-6
IDI1_000534
WLN: T6NJ BN1R&2N1&1 &GH
NCGC00018125-01
NCGC00018125-02
NCGC00018125-03
DA-78629
SBI-0051548.P002
CS-0009189
NS00003396
Benzyl-(.alpha.-pyridyl)-dimethylaethylendiamin
C07180
D08645
EN300-708778
Tripelennamine 1000 microg/mL in Acetonitrile
AB00053562_13
AB00053562_14
L000603
pyridine, 2-[benzyl(2-dimethylaminoethyl)amino]-
Q415203
1, N,N-dimethyl-N'-(phenylmethyl)-N'-2-pyridinyl-
BRD-K57033106-003-19-7
BRD-K57033106-048-02-8
BRD-K57033106-048-03-6
BRD-K57033106-048-04-4
N\'-benzyl-N,N-dimethyl-N\'-pyridin-2-ylethane-1,2-diamine
202-100-1