Interesting facts
Interesting Facts about N-benzyl-N-methyl-prop-2-yn-1-amine
N-benzyl-N-methyl-prop-2-yn-1-amine is a fascinating compound within the realm of organic chemistry and showcases various intriguing characteristics. This compound can be categorized as an alkyne amine due to its prop-2-yn-1-amine structure, which features a triple bond. Here are some interesting points to consider:
- Structural Complexity: The presence of both benzyl and methyl groups creates a unique structural arrangement, leading to a distinct reactivity profile. The substitution pattern can influence the compound's chemical behavior and interactions.
- Biological Activity: Compounds with similar structures often exhibit various biological activities. Researchers are continually exploring their potential as drug candidates, particularly for neuroactive or anti-cancer purposes.
- Synthetic Routes: The synthesis of N-benzyl-N-methyl-prop-2-yn-1-amine can involve innovative methods that utilize catalytic reactions. Techniques like alkylation or substitution reactions play a critical role in its preparation.
- Applications in Material Science: Due to its functional groups, this compound can potentially be used in the creation of specialized materials, including polymers or conductive films, combining chemistry with material engineering.
- Interdisciplinary Relevance: The study of this compound intersects with various fields such as pharmacology, materials science, and organic chemistry, making it a subject of interest from various scientific perspectives.
As scientists continue to explore the properties and applications of N-benzyl-N-methyl-prop-2-yn-1-amine, they uncover novel uses and deepen our understanding of its chemical behavior. "The beauty of chemistry lies in its complexity and the endless possibilities it offers for discovery." This sentiment encapsulates the ongoing fascination with compounds like this one.
Synonyms
pargyline
555-57-7
N-Methyl-N-propargylbenzylamine
Pargylamine
N-benzyl-N-methylprop-2-yn-1-amine
Paragyline
Eudatin
Supirdyl
Pargylin
Eutonyl
N-Methyl-N-2-propynylbenzylamine
Pargilina
Benzyl-methyl-2-propinylamin
Benzenemethanamine, N-methyl-N-2-propynyl-
Benzylmethylpropargylamine
N-Benzyl-N-methyl-2-propynylamine
N-Methyl-N-benzylpropynylamine
Eutron
Methylbenzylpropynylamine
MO 911
N-Benzyl-N-methyl-2-propyn-1-amine
BENZYLAMINE, N-METHYL-N-2-PROPYNYL-
Pargyline (INN)
Pargyline [INN]
A 19120
benzyl(methyl)(prop-2-yn-1-yl)amine
CHEMBL673
9MV14S8G3E
CHEBI:7930
N-methyl-N-(phenylmethyl)prop-2-yn-1-amine
Benzyl-methyl-prop-2-ynyl-amine
Pargylinum
Pargyline [INN:BAN]
Pargylinum [INN-Latin]
Pargilina [INN-Spanish]
Benzyl-methyl-2-propinylamin [Czech]
CCRIS 6740
Benzylmethylpropynylamine
NCGC00015841-02
CAS-306-07-0
EINECS 209-101-6
Lopac-P-8013
BRN 1938132
UNII-9MV14S8G3E
AI3-62058
MFCD00008576
Eutonyl (Salt/Mix)
Pargyline (Standard)
Spectrum_000641
PARGYLINE [MI]
Prestwick0_000183
Prestwick1_000183
Prestwick2_000183
Prestwick3_000183
Spectrum2_001039
Spectrum3_000540
Spectrum4_000469
Spectrum5_001030
PARGYLINE [VANDF]
CBChromo1_000308
PARGYLINE [WHO-DD]
SCHEMBL2045
Lopac0_001022
BSPBio_000105
BSPBio_002159
KBioGR_000918
KBioSS_001121
2-12-00-00548 (Beilstein Handbook Reference)
DivK1c_000053
SPBio_001257
SPBio_002026
BPBio1_000117
GTPL7262
HY-A0091AR
DTXSID3023423
DPWPWRLQFGFJFI-UHFFFAOYSA-
HY-A0091A
KBio1_000053
KBio2_001121
KBio2_003689
KBio2_006257
KBio3_001659
NINDS_000053
HMS3604I04
N-benzyl-N-methyl-2-propinylamine
Pargyline hydrochloride (Salt/Mix)
AAA55557
BDBM50172756
2-Propynylamine, N-benzyl-N-methyl-
N-Methyl-N-(2-propynyl)benzylamine-
AKOS009027469
N-benzyl-N-methyl-prop-2-yn-1-amine
N-Methyl-N-propargylbenzylamine, 97%
CCG-205102
CS-4685
DB01626
SDCCGSBI-0050995.P005
IDI1_000053
N-Benzyl-N-methyl-2-propyn-1-amine #
N-Methyl-N-(2-propyn-1-yl)benzylamine
NCGC00015841-01
NCGC00015841-03
NCGC00015841-04
NCGC00015841-05
NCGC00015841-06
NCGC00015841-07
NCGC00015841-18
NCGC00024240-03
AS-75650
SBI-0050995.P004
1ST169387
DB-072009
AB00053516
M2618
NS00000467
C07414
D08453
EN300-120295
T72610
AB00053516_13
N-benzyl-N-methylprop-2-yn-1-amine,hydrochloride
Q781329
BRD-K83597974-003-05-7
BRD-K83597974-003-22-2
Z103710848
InChI=1/C11H13N/c1-3-9-12(2)10-11-7-5-4-6-8-11/h1,4-8H,9-10H2,2H3
Solubility of N-benzyl-N-methyl-prop-2-yn-1-amine
N-benzyl-N-methyl-prop-2-yn-1-amine (C11H13N) is an organic compound known for its unique properties and applications. When considering the solubility of this compound, several factors play a crucial role:
In summary, while N-benzyl-N-methyl-prop-2-yn-1-amine demonstrates a tendency toward solubility in polar solvents due to the amine’s ability to form hydrogen bonds, it also shows significant solubility characteristics in organic solvents owing to its hydrophobic nature. Understanding these properties is essential for its effective use in chemical applications.