84312-87-8 Usage
Description
3-(4-OXO-3-P-TOLYL-3,4-DIHYDRO-QUINAZOLIN-2-YL)-PROPIONIC ACID is a synthetic organic compound characterized by a quinazoline core structure with a propionic acid group attached to the quinazoline ring. With a molecular formula of C19H18N2O3, this compound is recognized for its potential pharmacological activity, particularly in the realms of neurological disorders and cancer treatment. The presence of p-tolyl and propionic acid groups suggests that it may exhibit specific binding or functional characteristics within biological systems, warranting further research to elucidate its full spectrum of applications and effects.
Uses
Used in Pharmaceutical Research:
3-(4-OXO-3-P-TOLYL-3,4-DIHYDRO-QUINAZOLIN-2-YL)-PROPIONIC ACID is utilized as a research molecule for its potential pharmacological properties, specifically in the development of treatments for neurological disorders and cancer. Its unique structure and functional groups contribute to its potential as a therapeutic agent, warranting in-depth investigation into its interactions with biological targets and mechanisms of action.
Used in Drug Development:
In the pharmaceutical industry, 3-(4-OXO-3-P-TOLYL-3,4-DIHYDRO-QUINAZOLIN-2-YL)-PROPIONIC ACID is employed as a candidate compound in drug development pipelines. Its quinazoline core and attached functional groups may offer advantages in terms of binding affinity, selectivity, and pharmacokinetics, making it a promising starting point for the design of novel therapeutic agents.
Used in Cancer Treatment Research:
3-(4-OXO-3-P-TOLYL-3,4-DIHYDRO-QUINAZOLIN-2-YL)-PROPIONIC ACID is explored as a potential anticancer agent, given its structural features that may allow it to target specific pathways or cellular mechanisms involved in cancer progression. Its application in this field is driven by the need for new and effective treatments, particularly for cancers that are resistant to existing therapies.
Used in Neurological Disorder Treatment Research:
3-(4-OXO-3-P-TOLYL-3,4-DIHYDRO-QUINAZOLIN-2-YL)-PROPIONIC ACID is also considered for its potential role in the treatment of neurological disorders. Its quinazoline structure may confer neuroprotective or neuroregenerative properties, making it a valuable compound for research into conditions such as Alzheimer's disease, Parkinson's disease, and other neurodegenerative disorders.
Further research is essential to fully understand the potential uses and effects of 3-(4-OXO-3-P-TOLYL-3,4-DIHYDRO-QUINAZOLIN-2-YL)-PROPIONIC ACID, as its current applications are based on its chemical structure and the hypothesized biological activities associated with similar compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 84312-87-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,1 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84312-87:
(7*8)+(6*4)+(5*3)+(4*1)+(3*2)+(2*8)+(1*7)=128
128 % 10 = 8
So 84312-87-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H16N2O3/c1-12-6-8-13(9-7-12)20-16(10-11-17(21)22)19-15-5-3-2-4-14(15)18(20)23/h2-9H,10-11H2,1H3,(H,21,22)/p-1
84312-87-8Relevant articles and documents
Some Reactions of 2-(n-Propyl/β-carboxyethyl)-3,1-benzoxazin-4(H)-ones and 2-(n-Propyl/β-carboxyethyl)-4(3H)-quinazolinones
Essawy, A.,El-Hashash, M. A.,El-Gendy, A. M.,Hamad, M. M. M.
, p. 593 - 595 (2007/10/02)
Reaction of 2-(n-propyl/β-carboxyethyl)-3,1-benzoxazin-4-ones (1a,b) with aromatic amines gives 3-aryl-2-(n-propyl/β-carboxyethyl)-4(3H)-quinazolinones (2a-e).Compound 1a reacts with hydrazine hydrate and phenylhydrazine to give 3-amino-2-n-propyl-4(3H)-q
