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4-Methoxy-1-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile

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Identification
Molecular formula
C9H8N2O2
CAS number
3350-41-6
IUPAC name
4-methoxy-1-methyl-2-oxo-pyridine-3-carbonitrile
State
State

The compound is typically found in a solid state at room temperature and has moderate solubility in organic solvents.

Melting point (Celsius)
68.30
Melting point (Kelvin)
341.45
Boiling point (Celsius)
271.20
Boiling point (Kelvin)
544.35
General information
Molecular weight
176.17g/mol
Molar mass
176.1730g/mol
Density
1.2105g/cm3
Appearence

The compound appears as a white to off-white solid powder. It generally forms crystalline structures and can present a slightly yellow hue depending on impurities or storage conditions.

Comment on solubility

Solubility of 4-methoxy-1-methyl-2-oxo-pyridine-3-carbonitrile

The solubility of 4-methoxy-1-methyl-2-oxo-pyridine-3-carbonitrile can be influenced by various factors due to its unique chemical structure. This compound may exhibit varying degrees of solubility in different solvents. Here are some essential points to consider:

  • Polarity: The presence of the methoxy group can increase the polar character of the compound, potentially enhancing its solubility in polar solvents like water and ethanol.
  • Hydrogen Bonding: The carbonitrile (-C≡N) and ketone (C=O) functional groups can participate in hydrogen bonding, which could affect its solubility profile, allowing for better solubility in solvents that can form strong interactions.
  • Solvent Type: It is likely to be more soluble in organic solvents such as dichloromethane and acetone as compared to non-polar solvents due to polar interactions.
  • Concentration: Higher concentrations may lead to saturation, thus less solubility can be observed beyond a certain limit.

In conclusion, while specific solubility data might not be readily available for this compound, understanding its structure gives valuable insights into potential solubility behavior. The overall solubility should be evaluated through empirical testing in various solvents to determine practical applications.

Interesting facts

In-Depth Look at 4-Methoxy-1-Methyl-2-Oxo-Pyridine-3-Carbonitrile

The compound 4-methoxy-1-methyl-2-oxo-pyridine-3-carbonitrile is a fascinating member of the pyridine family, known for its diverse applications in medicinal chemistry and material science. As a derivative of pyridine, this compound features a range of functional groups that enhance its chemical versatility.

Key Characteristics

  • Pyridine Derivative: Pyridine rings are well-known in organic chemistry for their ability to participate in various chemical reactions.
  • Diverse Functional Groups: This compound's structure includes a methoxy group and a cyano group, which can influence reactivity and stability.
  • Pharmacological Potential: Compounds like this have been studied for their relevance in drug discovery due to their biological activity, making them worth exploring for potential therapeutic applications.

Applications and Uses

  • Synthetic Intermediates: This compound can serve as a key intermediate in the synthesis of more complex molecules.
  • Research Relevance: It is often explored in the context of developing novel pharmaceuticals and agrochemicals.
  • Material Science: Pyridine derivatives are also valuable in the production of dyes and polymers due to their unique electronic properties.

In conclusion, 4-methoxy-1-methyl-2-oxo-pyridine-3-carbonitrile presents a unique blend of structural attributes and functional capabilities that continue to pique the interest of chemists. As one studies its properties and applications, it's essential to appreciate how such compounds contribute significantly to advancing both scientific knowledge and practical applications in various fields.

Synonyms
RICININE
524-40-3
Ricinin
Ricidine
Ritsinin
Recinine
4-methoxy-1-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile
1,2-Dihydro-4-methoxy-1-methyl-2-oxonicotinonitrile
NSC 409913
NSC 642604
4-methoxy-1-methyl-2-oxopyridine-3-carbonitrile
3-Pyridinecarbonitrile, 1,2-dihydro-4-methoxy-1-methyl-2-oxo-
EINECS 208-359-7
UNII-130UFS7AE0
BRN 0139222
130UFS7AE0
CHEBI:18043
RICININE [MI]
NSC-409913
NSC-642604
Nicotinonitrile, 1,2-dihydro-4-methoxy-1-methyl-2-oxo-
DTXSID50200412
5-22-07-00318 (Beilstein Handbook Reference)
1,2-dihydro-4-methoxy-1-methyl-2-oxo-3-pyridimecarbonitrile
1,2-Dihydro-4-methoxy-1-methyl-2-oxo-Nicotinonitrile
4-Methoxy-1-methyl-2-oxo-1,2-dihydro-3-pyridinecarbonitrile
DTXCID50122903
3-cyano-4-methoxy-n-methyl-2-pyridone
3-Pyridinecarbonitrile, 1,2-dihydro-4-methoxy-1-methyl-2-oxo-(9CI)
208-359-7
petsayfqsgaeqy-uhfffaoysa-n
NSC409913
NSC642604
MFCD00171320
Prestwick_1041
Ricinine-(methyl-d3)
1,2-Dihydro-4-methoxy-1-methyl-2-oxo-3-pyridinecarbonitrile
Prestwick0_000678
Prestwick1_000678
Prestwick2_000678
Prestwick3_000678
TimTec1_001989
Oprea1_847597
BSPBio_000775
MLS001048969
SCHEMBL257955
SPBio_002696
4-methoxy-1-methyl-2-oxohydropyridine-3-carbonitrile
BPBio1_000853
MEGxp0_000747
CHEMBL1329957
ACon1_001266
WLN: T6NVJ A1 CCN DO1
GLXC-05239
HMS1539K09
HMS1570G17
HMS2097G17
HMS2268G21
TNP00192
CCG-36061
STL564798
AKOS003673683
Ricinine, >=95% (LC/MS-ELSD)
FR27726
FS-7365
NCGC00016487-01
NCGC00016487-02
NCGC00016487-03
NCGC00016487-04
NCGC00016487-05
NCGC00142397-01
NCGC00169517-01
NCGC00169517-02
CAS-524-40-3
SMR000386989
SY256804
DB-052124
HY-121944
CS-0083725
NS00015447
C01526
E88580
4-methoxy-1-methyl-2-oxo-pyridine-3-carbonitrile
Q907865
BRD-K82561139-001-01-9
BRD-K82561139-001-05-0
Nicotinonitrile,2-dihydro-4-methoxy-1-methyl-2-oxo-
3-Pyridinecarbonitrile,2-dihydro-4-methoxy-1-methyl-2-oxo-
1,2-Dihydro-1-methyl-4-methoxy-2-oxo-3-pyridine carbonitrile
1,2-Dihydro-4-methoxy-1-methyl-2-oxo-3-pyridinecarbonitrile;1,2-Dihydro-4-methoxy-1-methyl-2-oxonicotinonitrile;Recinine