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Nifedipine

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Identification
Molecular formula
C17H18N2O6
CAS number
21829-25-4
IUPAC name
diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate
State
State

Nifedipine is typically in the solid state at room temperature. It is usually available in a powder form for manufacturing or as a tablet for medicinal applications.

Melting point (Celsius)
172.00
Melting point (Kelvin)
445.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
346.36g/mol
Molar mass
346.3620g/mol
Density
1.3000g/cm3
Appearence

Diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate, commonly known as Nifedipine, typically appears as a yellow crystalline powder. It is sensitive to light and moisture, hence should be stored in a dry, light-resistant container.

Comment on solubility

Solubility of Diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate

Diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate is a compound that presents interesting solubility characteristics. Its solubility can be influenced by various factors, primarily due to its chemical structure and the presence of functional groups. Here are some key points regarding its solubility:

  • Polarity: This compound has both hydrophilic (water-attracting) and hydrophobic (water-repelling) regions. The presence of carboxylate groups contributes to its polar nature, which enhances solubility in polar solvents.
  • Solvent Compatibility: It is likely to be soluble in organic solvents such as ethanol, methanol, and acetone due to its ester and amine functionalities. However, its solubility in non-polar solvents may be limited.
  • Temperature Influence: The solubility may increase with temperature, which is a common trait for many organic compounds. Higher temperatures generally promote greater molecular interactions between solute and solvent.
  • Application in Synthesis: The solubility of this compound is crucial for its use in various organic synthesis reactions, where a high degree of solubility can enable more efficient reaction kinetics.

In conclusion, the solubility of diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate is determined by a combination of its molecular structure, functional groups, and the nature of the solvent used. Understanding these relationships can help optimize its application in different chemical contexts.

Interesting facts

Interesting Facts about Diethyl 2,4,6-Trimethyl-1,4-Dihydropyridine-3,5-Dicarboxylate

Diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate, often referred to as a member of the dihydropyridine family, is a fascinating compound that finds utility in various fields of research and application. Here are some key points about this compound:

  • Pharmacological Potential: Dihydropyridines are well-known in medicinal chemistry for their role as calcium channel blockers. This compound may exhibit similar properties, making it a candidate for cardiovascular therapy.
  • Versatile Synthesis: The synthesis of this compound typically involves multi-step organic reactions, which can highlight various techniques such as condensation, esterification, and cyclization. This allows chemists to explore different synthetic pathways and optimize yields.
  • Functional Group Diversity: The presence of both carboxylate and alkyl groups enhances the compound's reactivity and solubility, enabling it to participate in further chemical reactions, effectively broadening its applicability in organic synthesis and pharmaceuticals.
  • Study of Asymmetric Synthesis: The compound can serve as a model to study asymmetric synthesis, which is crucial in producing enantiomerically pure drugs. This highlights the importance of chirality in medicinal compounds.
  • Fun Fact: Dihydropyridines are often used in research concerning the structure-activity relationship (SAR), providing insights into how changes in molecular structure can influence biological activity.

Overall, diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate serves as a remarkable example of how organic compounds can be engineered for specific biological functions. The ongoing exploration of such compounds continually opens doors to new therapeutic possibilities and sustainable chemistry practices.

Synonyms
Diethyl 1,4-dihydro-2,4,6-trimethylpyridine-3,5-dicarboxylate
3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,4,6-trimethyl-, 3,5-diethyl ester
211-188-0
632-93-9
diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate
3,5-Diethoxycarbonyl-1,4-dihydro-2,4,6-collidine
DDC (porphyrinogen)
3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,4,6-trimethyl-, diethyl ester
Diethyl 1,4-dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylate
3,5-Diethoxycarbonyl-1,4-dihydrocollidine
NSC 49528
3,5-Dicarbethoxy-1,4-dihydrocollidine
DICARBETHOXYDIHYDROCOLLIDINE
NSC 8910
3,5-Bis(ethoxycarbonyl)-1,4-dihydrocollidine
1,4-Dihydro-3,5-dicarbethoxycollidine
CHEBI:83605
3,5-Dicarbethoxy-1,4-dihydro-2,4,6-trimethylpyridine
MLS000766200
NSC 8910;DDC
CHEMBL3409638
3,5-diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate
3,4-dihydrocollidine
1,5-dicarbethoxycollidine
2,4,6-Trimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester
DDC (VAN)
SMR000146672
3, 1,4-dihydro-2,4,6-trimethyl-, diethyl ester
EINECS 211-188-0
MFCD00005950
Maybridge1_000106
MixCom1_000194
Oprea1_040271
MLS000554355
SCHEMBL3503405
CHEMBL3189958
DTXSID6060898
NSC8910
HMS2564I21
NSC-8910
NSC49528
BDBM50073946
CCG-45634
NSC-49528
AKOS005208036
GS-5680
NCGC00246343-01
NCGC00246343-02
PD063982
DB-054451
DB-243409
HY-118594
CS-0067585
D0558
NS00018653
3,5-Diethoxycarbonyl-1,4-dihydro-s-collidine
F11713
SR-01000635388-1
Q27157006
diethyl2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate
diethyl 1,4-dihydro-2,4,6-trimethyl pyridine-3,5-dicarboxylate
Diethyl 2,4,6-trimethyl-1,4-dihydro-3,5-pyridinedicarboxylate #
1,4-Dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylic Acid Diethyl Ester
1,4-Dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylic acid, diethyl ester
Diethyl 1,4-dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylate, 99%