116235-62-2 Usage
Chemical structure
The compound has a complex structure with a dioxolo group, isoquinoline ring, and a 4-methoxyphenylmethyl group attached to the 5-position.
Potential biological activity
The presence of the dioxolo group and isoquinoline ring in its structure suggests that the compound may have biological activity.
Pharmacological properties
The 4-methoxyphenylmethyl group can contribute to the compound's pharmacological properties.
Tetrahydro structure
The compound has a ring system that includes four saturated carbon atoms, which may affect its chemical and physical properties.
Interest in medicinal chemistry and drug discovery
The compound's specific structure and potential biological activity make it a subject of interest for researchers in the field of medicinal chemistry and drug discovery.
Molecular weight
The molecular weight of the compound is approximately 323.37 g/mol.
Appearance
The compound is likely to be a solid at room temperature, although its exact appearance (e.g., color, crystal structure) is not specified in the provided material.
Solubility
The solubility of the compound in various solvents is not specified in the provided material, but it may be influenced by its chemical structure and functional groups.
Stability
The stability of the compound under different conditions (e.g., temperature, pH, light exposure) is not specified in the provided material, but it may be affected by its chemical structure and functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 116235-62-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,2,3 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 116235-62:
(8*1)+(7*1)+(6*6)+(5*2)+(4*3)+(3*5)+(2*6)+(1*2)=102
102 % 10 = 2
So 116235-62-2 is a valid CAS Registry Number.
116235-62-2Relevant academic research and scientific papers
Gandomkar, Somayyeh,Fischereder, Eva-Maria,Schrittwieser, Joerg H.,Wallner, Silvia,Habibi, Zohreh,Macheroux, Peter,Kroutil, Wolfgang
, p. 15051 - 15054 (2015)
N-Dealkylation methods are well described for organic chemistry and the reaction is known in nature and drug metabolism; however, to our knowledge, enantioselective N-dealkylation has not been yet reported. In this study, exclusively the (S)-enantiomers o
