132589-64-1 Usage
Structure
A derivative of isoquinolinecarboxylic acid with a benzoyl group attached to the 2-position of a tetrahydroisoquinoline ring.
Potential applications
Medicinal chemistry, particularly in the development of pharmaceuticals.
Biological activities
Exhibits interesting biological activities.
Synthesis
May be utilized as a building block for the synthesis of various drug candidates.
Research applications
May have potential as a tool compound in research applications.
Versatility
Diverse potential uses in the field of chemistry and pharmaceutical science.
Check Digit Verification of cas no
The CAS Registry Mumber 132589-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,8 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132589-64:
(8*1)+(7*3)+(6*2)+(5*5)+(4*8)+(3*9)+(2*6)+(1*4)=141
141 % 10 = 1
So 132589-64-1 is a valid CAS Registry Number.
132589-64-1Relevant academic research and scientific papers
Autoxidation of intermediary mesoionic 1,3-oxazolium-5-olates generated from cyclic N-acyl α-amino acids
Kawase, Masami
, p. 1248 - 1253 (2007/10/03)
Mesoionic 1,3-oxazolium-5-olates (munchnones) react fairly rapidly with oxygen to give the autoxidation products when the C-4 substituent is aromatic. The autoxidation occurred in the munchnones generated from N-acyl tetrahydroisoquinoline-1-carboxylic ac
