1093857-88-5 Usage
Uses
Used in Pharmaceutical Research and Development:
2,3-difluoro-4-methoxypropiophenone is utilized as a key intermediate in the synthesis of various pharmaceutical compounds due to its unique structure and reactivity. It aids in the creation of new drugs and agrochemicals, contributing to the advancement of medicinal chemistry.
Used in Organic Synthesis:
In the field of organic synthesis, 2,3-difluoro-4-methoxypropiophenone serves as a valuable building block for the production of a range of fine chemicals. Its specific functional groups facilitate targeted reactions, making it instrumental in the synthesis of complex organic molecules.
Used in Anticancer Research:
2,3-difluoro-4-methoxypropiophenone is recognized for its potential as an anticancer agent. It has demonstrated the ability to inhibit the growth of cancer cells in preliminary studies, positioning it as a promising candidate for further research and development in oncology.
Used in the Production of Fine Chemicals:
2,3-difluoro-4-methoxypropiophenone is also employed in the manufacturing process of various fine chemicals, where its distinct structural features and reactivity are leveraged to produce high-quality specialty chemicals for diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1093857-88-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,3,8,5 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1093857-88:
(9*1)+(8*0)+(7*9)+(6*3)+(5*8)+(4*5)+(3*7)+(2*8)+(1*8)=195
195 % 10 = 5
So 1093857-88-5 is a valid CAS Registry Number.
1093857-88-5Relevant articles and documents
PYRAZOLONE DERIVATIVE AND PDE INHIBITOR CONTAINING THE SAME AS ACTIVE INGREDIENT
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Page/Page column 148, (2010/04/25)
It is to provide a novel pyrazolone derivative represented by the following general formula (1), which is useful as a pharmaceutical and has a phosphodiesterase inhibitory action: wherein R1,R2: C1-6 alkyl; R3,R4: H, X, C1-6 alkoxy; Z:O, S; A:AA, BB, wherein AA represents wherein BB represents wherein R5: H, C1-6 alkyl ; R6,R7: C1-6 alkyl.
