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6,7-Dimethoxy-1,2-dimethyl-3,4-dihydroisoquinoline

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Identification
Molecular formula
C13H17NO2
CAS number
64877-65-6
IUPAC name
6,7-dimethoxy-1,2-dimethyl-3,4-dihydro-1H-isoquinoline
State
State

At room temperature, 6,7-Dimethoxy-1,2-dimethyl-3,4-dihydroisoquinoline is generally in a solid state, which is common for many organic compounds of this type. However, depending on the specific environmental conditions, it may also be observed as an oily liquid.

Melting point (Celsius)
94.00
Melting point (Kelvin)
367.15
Boiling point (Celsius)
314.00
Boiling point (Kelvin)
587.15
General information
Molecular weight
205.27g/mol
Molar mass
205.2690g/mol
Density
1.1300g/cm3
Appearence

6,7-Dimethoxy-1,2-dimethyl-3,4-dihydroisoquinoline typically appears as a colorless to pale yellow crystalline solid. It may sometimes be encountered as an oily liquid depending on purity and specific conditions.

Comment on solubility

Solubility of 6,7-dimethoxy-1,2-dimethyl-3,4-dihydro-1H-isoquinoline

The solubility of a compound plays a crucial role in its reactivity, bioavailability, and overall applications. For 6,7-dimethoxy-1,2-dimethyl-3,4-dihydro-1H-isoquinoline, the solubility characteristics can be outlined as follows:

  • Polarity: Given its structure, this compound possesses a non-polar moiety due to the isoquinoline framework, which typically leads to lower solubility in polar solvents.
  • Solvent Interactions: It is more likely to exhibit solubility in non-polar solvents such as chloroform or ethyl acetate, while solubility in water may be limited.
  • Temperature Dependency: Like many organic compounds, solubility may increase with temperature. Heating a solution can often enhance the solubility of 6,7-dimethoxy-1,2-dimethyl-3,4-dihydro-1H-isoquinoline in suitable organic solvents.

It is vital to recognize that, as with most compounds, solubility can vary significantly based on environmental conditions such as pH, temperature, and the presence of other solutes. Therefore, understanding these aspects is key for effective applications in pharmaceuticals and organic synthesis.

Interesting facts

Interesting Facts about 6,7-Dimethoxy-1,2-dimethyl-3,4-dihydro-1H-isoquinoline

This intriguing compound, known as 6,7-dimethoxy-1,2-dimethyl-3,4-dihydro-1H-isoquinoline, represents a fascinating class of organic molecules called isoquinolines. These compounds are characterized by their unique bicyclic structure which makes them of keen interest in medicinal chemistry and organic synthesis.

Key Features

  • Structural Diversity: Isoquinolines can be synthesized in various forms which allows them to exhibit a wide range of biological activities.
  • Potential Pharmacological Activities: Many isoquinoline derivatives have been studied for their potential medicinal properties, including anti-inflammatory, anticancer, and antimicrobial effects.
  • Natural Occurrence: Some naturally occurring isoquinolines, such as those found in plants, are utilized in traditional medicine, showcasing the compound's linkage to both biology and chemistry.

As a scientist, one cannot overlook the intriguing complexity of the dimethoxy and dimethyl substitutions present in this compound. These modifications can significantly influence the compound's chemical behavior and biological effects. The methoxy groups, in particular, can enhance solubility and modulate the compound’s reactivity, while the dimethyl substitution can impact sterics and electronic properties.

Applications in Research

Research into compounds like 6,7-dimethoxy-1,2-dimethyl-3,4-dihydro-1H-isoquinoline can also provide insights into:

  • Drug design and discovery, as chemists seek to create derivatives with enhanced efficacy and reduced side effects.
  • Investigating the mechanism of action of isoquinoline-related compounds in various biological pathways.
  • Developing analytical chemistry techniques to study these complex molecules further.

Overall, this compound is just one example of how the world of organic chemistry provides endless opportunities for discovery and innovation in both scientific research and practical applications.

Synonyms
Carnegine
Pectenine
Carnegin
Pectenin
490-53-9
EOW70A27WK
CARNEGINE [MI]
(.+/-.)-Pectenine
UNII-EOW70A27WK
Isoquinoline, 1,2,3,4-tetrahydro-6,7-dimethoxy-1,2-dimethyl-, (.+/-.)-
Isoquinoline, 1,2,3,4-tetrahydro-6,7-dimethoxy-1,2-dimethyl-
(+-)-1,2,3,4-Tetrahydro-6,7-dimethoxy-1,2-dimethylisoquinoline
Isoquinoline, 1,2,3,4-tetrahydro-6,7-dimethoxy-1,2-dimethyl-, (+-)-
(+-)-PECTENINE
(+-)-CARNEGIN
(+-)-PECTENIN
hrsipkssevrspg-uhfffaoysa-n
(+/-)-CARNEGINE
6,7-dimethoxy-1,2-dimethyl-3,4-dihydro-1H-isoquinoline
(+/-)-PECTENINE
(+/-)-CARNEGIN
(+/-)-PECTENIN
SCHEMBL1760713
CHEMBL5272718
DTXSID30871689
6,7-Dimethoxy-1,2-dimethyl-1,2,3,4-tetrahydroisoquinoline
AKOS038481513
RTE3_000038
BCB03_000701
Q27277280
6,7-Dimethoxy-1,2-dimethyl-1,2,3,4-tetrahydroisoquinoline #