54503-93-4 Usage
Uses
Used in Pharmaceutical Research:
4-CHLORO-6-PIPERIDINO-5-PYRIMIDINECARBALDEHYDE is used as a research compound for its potential therapeutic applications, particularly in the development of new drugs targeting various diseases. Its antitumor and antifungal properties make it a valuable asset in the discovery of novel treatments.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-CHLORO-6-PIPERIDINO-5-PYRIMIDINECARBALDEHYDE is utilized as a key intermediate in the synthesis of pharmaceutical compounds. Its unique structure allows for the creation of new molecules with potential therapeutic benefits.
Used in Drug Synthesis:
4-CHLORO-6-PIPERIDINO-5-PYRIMIDINECARBALDEHYDE is used as a building block in the synthesis of novel pharmaceutical compounds, contributing to the development of innovative drugs with improved efficacy and reduced side effects.
Used in Anticancer Applications:
In oncology, 4-CHLORO-6-PIPERIDINO-5-PYRIMIDINECARBALDEHYDE is employed as an anticancer agent, leveraging its antitumor properties to target and inhibit the growth of cancer cells, offering a potential new avenue for cancer treatment.
Used in Antifungal Applications:
In the realm of antifungal therapy, 4-CHLORO-6-PIPERIDINO-5-PYRIMIDINECARBALDEHYDE is used to combat fungal infections, providing a new approach to treating various fungal diseases and contributing to the development of more effective antifungal medications.
Check Digit Verification of cas no
The CAS Registry Mumber 54503-93-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,0 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54503-93:
(7*5)+(6*4)+(5*5)+(4*0)+(3*3)+(2*9)+(1*3)=114
114 % 10 = 4
So 54503-93-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H12ClN3O/c11-9-8(6-15)10(13-7-12-9)14-4-2-1-3-5-14/h6-7H,1-5H2
54503-93-4Relevant academic research and scientific papers
Nikpour, Mohsen,Hasanzadeh, Neda
, p. 4380 - 4384 (2020)
Reaction of 4,6-dichloropyrimidine-5-carbaldehyde with amines in chloroform gave 4-(substitutedamino)-6-chloro-pyrimidine-5-carbaldehydes derivatives at low temperature. Treatment of the latter products with 2-aminobenzenethiol in alkaline benzene and the
New method for the synthesis of thieno[2,3-d]pyrimidines
Ryabova,Evstratova,Makarov,Tafeenko,Granik
, p. 1352 - 1358 (2007/10/03)
The reaction of 5-formyl-4-thiocyanatopyrimidines with nitromethane was studied under various conditions. The reaction was found unexpectedly to proceed with closure of a thiophene ring to give thieno[2,3-d]pyrimidines. The use of ammonium acetate as the catalyst leads to a side reaction involving closure of an isothiazole ring to give isothiazolo[5,4-d]pyrimidines. X-ray diffraction crystallographic analysis was used to confirm the structure of thieno[2,3-d]pyrimidine.
