480-73-9 Usage
Chemical class
Heterocyclic chemical compound
THPQ is a heterocyclic compound, which means it contains one or more rings of atoms with at least one atom being different from carbon.
Derivative class
Pyrroloquinoline derivatives
THPQ belongs to a specific class of heterocyclic compounds known as pyrroloquinoline derivatives.
Molecular structure
Fused tetracyclic ring system
The compound has a complex molecular structure, featuring a fused tetracyclic ring system, which means four rings are interconnected.
Potential applications
Medicinal chemistry and drug development
THPQ has potential applications in the fields of medicinal chemistry and drug development due to its unique structure and properties.
Biological activities
Antitumor agent
The compound has been studied for its biological activities, with a focus on its potential as an antitumor agent.
Research interest
Synthetic and medicinal chemistry
THPQ's unique structure and properties make it an interesting target for research in synthetic and medicinal chemistry.
Development potential
Novel pharmaceutical agent
The compound has the potential to be developed as a novel pharmaceutical agent, pending further studies.
Further studies needed
Therapeutic uses and mechanisms of action
Additional research is required to explore THPQ's potential therapeutic uses and to understand its mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 480-73-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 480-73:
(5*4)+(4*8)+(3*0)+(2*7)+(1*3)=69
69 % 10 = 9
So 480-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H13N/c1-3-9-5-2-7-12-8-6-10(4-1)11(9)12/h1,3-4H,2,5-8H2
480-73-9Relevant articles and documents
Synthesis, Structure, and Properties of Amino-Substituted Benzhydrylium Ions – A Link between Ordinary Carbocations and Neutral Electrophiles
Mayer, Robert J.,Hampel, Nathalie,Mayer, Peter,Ofial, Armin R.,Mayr, Herbert
, p. 412 - 421 (2018/09/14)
Optimized synthetic procedures for the straightforward access to eleven amino-substituted diarylmethylium tetrafluoroborates are described. These benzhydrylium ions cover a range of seven orders of magnitude in electrophilicity and provide a link between ordinary carbocations and neutral electrophiles. Five of these highly stabilized benzhydrylium tetrafluoroborates were characterized by single-crystal X-ray crystallography. While the experimentally determined bond lengths and angles in the solid state perfectly agree with those calculated by DFT methods for the gas phase and aqueous solution, crystal packing accounts for large differences in the twist angles of the aryl groups found in the solid state as compared to calculated structures.
1H and 13C studies of para-substituted benzaldoximes for evaluation of the electron donor properties of substituted amino groups
Gawinecki, Ryszard,Kolehmainen, Erkki,Kauppinen, Reijo
, p. 25 - 30 (2007/10/03)
1H and 13C NMR spectra of seventeen (E)-benzaldoximes and three acetophenone oximes, both carrying substituted p-amino groups, have been recorded and discussed from the point of view of substituent effect.The resonance effect of these substituents is not transmitted strongly to CH=NOH group.However, it is found that the chemical shift of Cpara depends linearly on ?R0 values.This dependence has been used to calculate the resonance substituent constants for the less common amino groups and the 1-pyrrolidine group is found to be the most powerful electron donor among the substituents studied.
