98276-70-1 Usage
Description
3,5-Diacetylpyrazole is a bifunctional pyrazole building block characterized by the presence of two acetyl groups at the 3 and 5 positions of the pyrazole ring. This organic compound serves as a versatile intermediate in the synthesis of various pharmaceutical compounds due to its unique chemical properties and reactivity.
Uses
Used in Pharmaceutical Industry:
3,5-Diacetylpyrazole is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its presence in the molecular structure allows for the development of new drugs with potential therapeutic applications, such as anti-inflammatory, analgesic, and antipyretic properties.
Used in Medicinal Chemistry Research:
3,5-Diacetylpyrazole is utilized as a building block in medicinal chemistry research to explore novel drug candidates. Its unique structure and reactivity enable the design and synthesis of new molecules with improved pharmacological properties, such as enhanced potency, selectivity, and reduced side effects.
Used in Drug Development:
3,5-Diacetylpyrazole plays a crucial role in drug development, as it can be incorporated into the molecular structure of new drug candidates. This allows researchers to optimize the pharmacokinetic and pharmacodynamic properties of these compounds, leading to the development of more effective and safer medications for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 98276-70-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,2,7 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98276-70:
(7*9)+(6*8)+(5*2)+(4*7)+(3*6)+(2*7)+(1*0)=181
181 % 10 = 1
So 98276-70-1 is a valid CAS Registry Number.
98276-70-1Relevant articles and documents
Efficient syntheses of some versatile 3,5-bifunctional pyrazole building blocks
Sachse, Anna,Penkova, Larysa,Noel, Gilles,Dechert, Sebastian,Varzatskii, Oleg A.,Fritsky, Igor O.,Meyer, Franc
, p. 800 - 806 (2008/09/21)
A series of convenient synthetic procedures are reported for pyrazole derivatives with carbonyl or ester groups in the 3- and 5-positions and variable substitution pattern at C4 and at the functional side arms. All compounds have been characterized by 1H and 13C NMR spectroscopy, elemental analyses, and mass spectrometry. In addition, the structures of several pyrazole derivatives have been determined by single crystal X-ray diffraction, which provides insight into the effect of functional side arms on the hydrogen-bonded supramolecular motifs of NH-pyrazoles. Georg Thieme Verlag Stuttgart.
