112009-28-6 Usage
Uses
Used in Pharmaceutical Synthesis:
1,5-DIPHENYL-1H-PYRAZOLE-3-CARBALDEHYDE is used as a key intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs due to its unique chemical properties and reactivity.
Used in Agrochemical Production:
In the agrochemical industry, 1,5-DIPHENYL-1H-PYRAZOLE-3-CARBALDEHYDE is utilized as a building block in the creation of agrochemicals, playing a crucial role in the formulation of effective and targeted pest control solutions.
Used in Organic Synthesis:
1,5-DIPHENYL-1H-PYRAZOLE-3-CARBALDEHYDE is employed as a reagent in organic chemistry for the preparation of pyrazole-based heterocyclic compounds, which are valuable for their diverse applications in chemical research and industry.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1,5-DIPHENYL-1H-PYRAZOLE-3-CARBALDEHYDE is used for the design and development of innovative drugs, leveraging its potential to form biologically active molecules with therapeutic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 112009-28-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,0,0 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112009-28:
(8*1)+(7*1)+(6*2)+(5*0)+(4*0)+(3*9)+(2*2)+(1*8)=66
66 % 10 = 6
So 112009-28-6 is a valid CAS Registry Number.
112009-28-6Relevant academic research and scientific papers
La(OTf)3-catalysed one-pot synthesis of pyrazole tethered imidazo[1,2-: A] azine derivatives and evaluation of their light emitting properties
Sharma, Shubham,Paul, Avijit Kumar,Singh, Virender
supporting information, p. 684 - 694 (2020/01/31)
A facile and efficient protocol has been unfolded towards the diversity-oriented synthesis of highly fluorescent pyrazole C-3(5) tethered imidazo[1,2-a]azines via an La(OTf)3 catalysed one-pot multicomponent assembly of pyrazole carbaldehydes, 2-aminoazines and isonitriles. This present protocol offers several advantages such as multiple bond formation in a single step, low catalyst loading, short reaction time, appreciable atom economy, good functional group tolerance, scalability and easy to perform reaction conditions. The optical properties of pyrazolyl imidazo[1,2-a]azines were also studied, and they exhibited an excellent fluorescence quantum yield (ΦF up to 83%).
