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2,2-dimethyl-1-oxido-3,4-dihydropyrrol-1-ium

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Identification
Molecular formula
C6H12N1O1
CAS number
12345-67-8
IUPAC name
2,2-dimethyl-1-oxido-3,4-dihydropyrrol-1-ium
State
State

At room temperature, 2,2-dimethyl-1-oxido-3,4-dihydropyrrol-1-ium is typically in a solid state. The compound's crystalline nature is due to its structured molecular configuration.

Melting point (Celsius)
75.00
Melting point (Kelvin)
348.15
Boiling point (Celsius)
223.00
Boiling point (Kelvin)
496.15
General information
Molecular weight
99.13g/mol
Molar mass
99.1280g/mol
Density
1.0123g/cm3
Appearence

This compound is a crystalline solid. It typically forms colorless to off-white crystals. Depending on purity, the appearance can vary slightly, leading to a pale yellowish tint in less pure samples.

Comment on solubility

Solubility of 2,2-dimethyl-1-oxido-3,4-dihydropyrrol-1-ium (C6H12N1O1)

The solubility of 2,2-dimethyl-1-oxido-3,4-dihydropyrrol-1-ium can be quite notable due to the presence of its functional groups that facilitate interaction with solvents. Here are some important aspects to consider:

  • Apolar Solvents: This compound is expected to have limited solubility in nonpolar solvents due to its charged nature.
  • Polar Solvents: It is more likely to be soluble in polar solvents such as water, methanol, and ethanol. The positively charged nitrogen can interact favorably with the dipoles of water molecules.
  • Hydrogen Bonding: The presence of the oxido group can enhance interactions through hydrogen bonding, thereby increasing solubility in polar environments.

In summary, 2,2-dimethyl-1-oxido-3,4-dihydropyrrol-1-ium demonstrates a tendency to dissolve in polar solvents while exhibiting low solubility in nonpolar solvents. This characteristic makes it suitable for applications where interaction with polar media is essential.

Interesting facts

Interesting Facts About 2,2-Dimethyl-1-oxido-3,4-dihydropyrrol-1-ium

2,2-Dimethyl-1-oxido-3,4-dihydropyrrol-1-ium is a fascinating compound that belongs to a class of organic chemicals known as pyrrolidines. This compound has garnered attention in various fields, particularly in synthetic chemistry and pharmaceuticals.

Key Aspects of 2,2-Dimethyl-1-oxido-3,4-dihydropyrrol-1-ium:

  • Structural Features: The molecular structure of this compound features a pyrrolidine ring with two methyl groups and an oxido group. This unique arrangement leads to interesting reactivity.
  • Applications: It has been studied for its potential applications in the production of new pharmaceuticals and as an intermediate in organic synthesis. Researchers often explore its use in creating bioactive molecules.
  • Reactivity: The presence of the oxido group significantly influences the compound's chemical behavior, which can include involvement in redox reactions, making it a valuable candidate for studying electron transfer processes.

Furthermore, compounds of this nature may also exhibit unique properties due to *steric hindrance* introduced by the dimethyl groups. As chemist Wolfgang Pauli famously said, "In science, there is no reality except that which is calculated." This idea resonates with the exploration of such compounds, as their properties often yield unexpected surprises upon thorough investigation.

In conclusion, 2,2-dimethyl-1-oxido-3,4-dihydropyrrol-1-ium is not just a chemical formula; it represents an intriguing realm of research opportunities that continuously enriches our understanding of organic chemistry and contributes to innovation in various scientific disciplines.

Synonyms
3317-61-1
5,5-Dimethyl-1-pyrroline N-oxide
DMPO
5,5-Dimethyl-1-pyrroline-N-oxide
5,5-Dimethyl-1-pyrroline-1-oxide
2,2-Dimethyl-3,4-dihydro-2H-pyrrole 1-oxide
2,2-dimethyl-1-oxido-3,4-dihydropyrrol-1-ium
5,5-Dimethylpyrroline-N-oxide
MFCD00005279
CHEBI:149489
5,5-dimethyl-1-pyrroline nitrone
7170JZ1QF3
A 2008L
5,5-DMPO
DMPO-5,5
2,2-Dimethyl-3,4-dihydro-2H-pyrrole N-Oxide; 5,5-Dimethyl-1-pyrroline 1-Oxide; 5,5-Dimethyl-4,5-dihydro-3H-pyrrole N-Oxide; 5,5-Dimethyl-?1-pyrroline 1-Oxide; 5,5-Dimethyl-?1-pyrroline N-Oxide; DMPO
2H-Pyrrole, 3,4-dihydro-2,2-dimethyl-, 1-oxide
5,5-Dimethyl-1-Pyrrolidine-N-oxide
5,5-DIMETHYL-1-PYRROLINEN-OXIDE
Lopac-D-5766
5,5DimethylpyrrolineNoxide
DMPO [MI]
Lopac0_000350
5,5-Dimethylpyrroline-Noxide
5,5Dimethyl1pyrroline Noxide
MLS002153283
CHEMBL79824
SCHEMBL130517
DTXSID30186826
VCUVETGKTILCLC-UHFFFAOYSA-N
HMS3261E21
Tox21_500350
BBL102694
STL556499
AKOS005257654
CCG-204445
FD64708
LP00350
SDCCGSBI-0050338.P002
3,4Dihydro2,2dimethyl2Hpyrrole 1oxide
NCGC00015351-01
NCGC00015351-02
NCGC00015351-03
NCGC00015351-04
NCGC00015351-06
NCGC00093786-01
NCGC00093786-02
NCGC00261035-01
AS-15638
DA-72844
SMR000326756
SY033062
5,5-Dimethyl-1-pyrroline N-oxide, 97%
2HPyrrole, 3,4dihydro2,2dimethyl, 1oxide
HY-107690
CS-0029209
D2362
EU-0100350
NS00050186
5,5-Dimethyl-1-pyrroline N-oxide, >=97%
D 5766
SR-01000075491
SR-01000075491-1
Q27265933
5,5-Dimethyl-1-pyrroline N-oxide, for ESR-spectroscopy
222-011-1