Skip to main content

Stepholidine

ADVERTISEMENT
Identification
Molecular formula
C20H23NO4
CAS number
113854-55-6
IUPAC name
2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline
State
State

At room temperature, Stepholidine is in a solid state due to its crystalline structure. It is stable under normal laboratory conditions, but should be stored in a cool and dry place to maintain its integrity.

Melting point (Celsius)
235.00
Melting point (Kelvin)
508.15
Boiling point (Celsius)
672.00
Boiling point (Kelvin)
945.15
General information
Molecular weight
337.37g/mol
Molar mass
337.3700g/mol
Density
1.1280g/cm3
Appearence

Stepholidine typically appears as pale yellow crystals or a crystalline powder. It is often provided in a purified form for research purposes. The appearance might vary slightly based on its purity and the form in which it is provided (e.g., hydrous or anhydrous).

Comment on solubility

Solubility of 2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline

The compound 2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline (C20H23NO4) displays interesting solubility characteristics.

Key Points about Solubility:

  • Solvent Dependence: The solubility of this compound is highly dependent on the solvent used, typically being more soluble in polar solvents.
  • General Trends: Compounds with multiple methoxy groups, like this one, often exhibit better solubility in organic solvents such as ethanol or dimethyl sulfoxide (DMSO).
  • Temperature Effects: Increasing the temperature may enhance its solubility, as is common with many organic compounds.
  • pH Influence: The solubility may vary with changes in pH, so it is crucial to test in various conditions.

In conclusion, while the solubility of 2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline can be challenging to predict, understanding its behavior in different solvents and conditions allows for better handling and application of this intriguing compound.

Interesting facts

Interesting Facts about 2,3,9,10-Tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline

2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline is a fascinating compound that presents a unique combination of structural features, making it a topic of interest in various fields of research. Here are some intriguing facts about this compound:

  • Complex Structure: The compound contains a highly complex framework, including multiple methoxy groups and a tetrahydroisoquinoline core, which suggests potential for diverse biological activities.
  • Potential Applications: Due to its structural attributes, it may show promise as a lead compound in drug development, particularly in the exploration of novel pharmacological properties.
  • Natural Occurrence: Similar isoquinoline derivatives have been found in various natural sources, hinting at their roles in plant defense mechanisms and medicinal properties.
  • Symmetry and Chirality: The presence of multiple substituents on a cyclic structure contributes to chirality, allowing for isomer variation, which can significantly affect biological interactions.
  • Research Interest: Its intricate architecture makes it a compound of interest for synthetic organic chemistry, as chemists explore methods to construct such complex molecules.

As chemists delve into the research of compounds like this one, the exploration of their chemical reactivity, stability, and potential therapeutic effects continues to contribute to the expanding horizon of medicinal chemistry. The interplay between structural attributes and biological activity remains a captivating area of study.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This applies beautifully to the study of complex compounds, where each structural variation may lead to groundbreaking discoveries in health and science.

Synonyms
tetrahydropalmatine
2934-97-6
DL-Tetrahydropalmatine
10097-84-4
6H-Dibenzo[a,g]quinolizine, 5,8,13,13a-tetrahydro-2,3,9,10-tetramethoxy-
MFCD03265591
Hyndarin
2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline
Tetrahydropalmatine, (+/-)-
CHEMBL187892
78F8583LNQ
ROTUNDINUM
2,3,9,10-Tetramethoxy-5,8,13,13a-tetrahydro-6H-isoquino[3,2-a]isoquinoline
2,3,9,10-Tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[3,2-a]isoquinoline
Palmatine, Tetrahydro derivative of
GNF-Pf-3943
Tetrahydropalmatine, dl-
Tetrahydropalmatine [MI]
(+-)-Corydalis B
DTXSID20864207
6H-Dibenzo[a,g]quinolizine,5,8,13,13a-tetrahydro-2,3,9,10-tetramethoxy-
UNII-78F8583LNQ
(-)-Tetrahydropalmatine;L-Tetrahydropalmatine
Spectrum_001554
SpecPlus_000956
Spectrum2_000736
Spectrum3_001650
Spectrum4_001749
Spectrum5_000578
Tetrahydropalmatine ,(S)
Oprea1_616043
Oprea1_801288
BSPBio_003379
KBioGR_002198
KBioSS_002034
MLS006011812
DivK1c_007052
SCHEMBL230849
SPECTRUM1504178
Tetrahydropalmatine (Standard)
SPBio_000692
MEGxp0_000623
ACon1_002069
CHEBI:91709
HY-N0300R
KBio1_001996
KBio2_002034
KBio2_004602
KBio2_007170
KBio3_002599
HMS3428E01
HMS3886C12
BCP13567
HY-N0300
BBL028394
BDBM50170666
CCG-40142
MFCD00214191
s5559
STK395032
AKOS000276804
AKOS016186982
FD10012
FT66540
SDCCGMLS-0015237.P002
6H-Dibenzo(a,g)quinolizine, 5,8,13,13a-tetrahydro-2,3,9,10-tetramethoxy-, (+-)-
NCGC00073008-02
NCGC00073008-03
NCGC00073008-04
NCGC00095840-01
NCGC00095840-02
NCGC00095840-03
1ST10243
AS-12924
SMR004703491
SY108222
DB-047567
T3650
A19519
AB00053100-09
AA-504/21003028
AE-508/21133034
AE-508/21133037
AN-706/21186100
BRD-A43940795-001-02-8
BRD-A43940795-001-03-6
Q27163527
3,4,10,11-tetramethoxy-7,8,12b,13-tetrahydro-5H-6-azatetraphene
5,8,13,13a-Tetrahydro-2,3,9,10-tetramethoxy-6H- dibenzo[a,g]quinolizine
2,3,9,10-Tetramethoxy-5,8,13,13a-tetrahydro-6H-isoquinolino[3,2-a]isoquinoline
6H-Dibenzo[a,g]quinolizine, 5,8,13,13a-tetrahydro-2,3,9,10-tetramethoxy-, (.+/-.)-