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Noopept

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Identification
Molecular formula
C17H22N2O4
CAS number
157115-85-0
IUPAC name
ethyl 15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18),16-pentaene-17-carboxylate
State
State

At room temperature, Noopept is a solid white powder.

Melting point (Celsius)
96.00
Melting point (Kelvin)
369.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
318.41g/mol
Molar mass
318.4110g/mol
Density
1.1990g/cm3
Appearence

Noopept is typically a white crystalline powder. It is easily soluble in liquids and may present in the form of fine, white crystals or powder.

Comment on solubility

Solubility of Ethyl 15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18),16-pentaene-17-carboxylate (C17H22N2O4)

The solubility of ethyl 15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18),16-pentaene-17-carboxylate in various solvents can be quite intriguing and is influenced by several factors.

This compound features a complex chemical structure, which generally suggests variable solubility characteristics. Here are some key points concerning its solubility:

  • Polar vs. Nonpolar Solvents: The presence of a carboxylate group may enhance solubility in polar solvents, such as water or alcohols.
  • Hydrophobic Regions: Conversely, the polycyclic structure may also create substantial hydrophobic sections, leading to poor solubility in highly polar environments.
  • Temperature Influence: Solubility could be affected by temperature; typically, an increase in temperature can increase solubility, particularly for solutes with larger molecular weights.
  • pH Levels: The solubility can also be pH-dependent, with the carboxylate functional group potentially ionizing and enhancing solubility in alkaline conditions.

In summary, the solubility of C17H22N2O4 is likely to be multifaceted and should be evaluated comprehensively depending on the solvent systems employed and the specific conditions present. Understanding these aspects can be crucial in applications involving this complex compound.

Interesting facts

Interesting Facts about Ethyl 15-Ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18),16-pentaene-17-carboxylate

Ethyl 15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18),16-pentaene-17-carboxylate represents a fascinating class of chemical compounds known as diazabicyclic compounds. Here are some intriguing aspects of this compound:

  • Complex Structure: The compound features a highly intricate bicyclic structure, which contributes to its unique chemical behavior and potential applications.
  • Applications in Chemistry: Such complex molecules may have potential applications in medicinal chemistry, particularly in pharmaceuticals where they can be explored for their biological activities.
  • Electrophilic Properties: The presence of both nitrogen and various double bonds in its structure gives it varied electrophilic properties, possibly making it an interesting candidate for further reactions in organic synthesis.
  • Synthetic Pathways: The synthesis of ethyl 15-ethyl-1,11-diazapentacyclo compounds often requires advanced techniques in organic synthesis, showcasing the skill and innovation of contemporary chemists.

As a chemistry student, delving into such compounds can be quite rewarding due to the combination of theoretical knowledge and practical skills applied in their study. It encourages a deeper appreciation for the richness of chemical diversity and the constant evolution of synthetic methodologies.

In summary, compounds like ethyl 15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18),16-pentaene-17-carboxylate challenge our understanding of chemical frameworks and continually inspire innovative research in chemistry.

Synonyms
Ethyl eburnamenine-14-carboxylate
Ethyl apovincaminate
77549-94-1
ethyl 15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18),16-pentaene-17-carboxylate
Eburnamenine-14-carboxylic acid, ethyl ester, (3.alpha.,16.alpha.)-
LSM-5249
Eburnamenine-14-carboxylic acid, ethyl ester
Vinpocetine Impurity E
Ethyl trans-apovincaminate
MLS006011923
SCHEMBL7947532
CHEMBL1367774
BDBM86220
CHEBI:91571
DTXSID90860599
DDNCQMVWWZOMLN-UHFFFAOYSA-N
HMS3266B06
ALBB-022444
BCP33392
BCP33393
BCP33394
LSM-1372
BBL006569
STL135992
Vinpocetine trans-(3S,16R) Isomer
AKOS005747008
CAS_443955
NSC_443955
NCGC00016854-02
NCGC00163690-01
NCGC00163690-02
AS-11611
SMR001828549
BRD-A19374631-001-01-0
Q27163405
Vinpocetine Impurity F;(-)-Apovincaminic acid ethyl ester
ETHYL 15-ETHYL-1,11-DIAZAPENTACYCLO[9.6.2.0(2),?.0?,(1)?.0(1)?,(1)?]NONADECA-2,4,6,8(18),16-PENTAENE-17-CARBOXYLATE