161644-16-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
A derivative is a compound that is structurally related to another compound, in this case, quinoline.
Explanation
A heterocyclic compound is a ring-shaped molecule containing atoms of at least two different elements, with quinoline being an aromatic compound.
Explanation
This is another way to refer to the same chemical compound, emphasizing the presence of a methyl group at the 6th position.
Explanation
The compound is mainly used for scientific research and in laboratory settings to study its properties and potential applications.
Explanation
The compound has been found to possess properties that may have an effect on living organisms, making it of interest for drug development.
Explanation
Due to its pharmacological properties, the compound has been studied for its potential use in the development of new drugs.
Explanation
The compound may have potential applications in the field of medicinal chemistry, particularly in the development of novel therapeutic agents.
Explanation
More research is required to fully understand the potential uses and effects of this chemical compound, including its safety, efficacy, and optimal applications.
Derivative of Quinoline
Yes
Heterocyclic Aromatic Compound
Yes
Primary Use
Research and Laboratory Applications
Pharmacological Properties
Yes
Potential Drug Development
Yes
Applications in Medicinal Chemistry
Yes
Further Research Needed
Yes
Check Digit Verification of cas no
The CAS Registry Mumber 161644-16-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,6,4 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 161644-16:
(8*1)+(7*6)+(6*1)+(5*6)+(4*4)+(3*4)+(2*1)+(1*6)=122
122 % 10 = 2
So 161644-16-2 is a valid CAS Registry Number.
161644-16-2Relevant articles and documents
Transformation of oximes of phenetyl ketone derivatives to quinolines and azaspirotrienones catalyzed by tetrabutylammonium perrhenate and trifluoromethanesulfonic acid
Kusama,Yamashita,Uchiyama,Narasaka
, p. 965 - 975 (2007/10/03)
Phenethyl ketone oximes are converted to quinolines by the treatment with tetrabutylammonium perrhenate, trifluoromethanesulfonic acid, and chloranil in refluxing 1,2-dichloroethane. Azaspirotrienones can be synthesized from p-hydroxyphenethyl or 3-(p-hydroxyphenyl)propyl ketone oximes by applying the above method. Thus prepared azaspirotrienones are converted to quinolines by acid treatment.
