25854-83-5 Usage
Description
1-BENZYL-3-PROPENYLOXY-1H-INDAZOLE is an organic compound with the chemical structure featuring a benzyl group at the 1st position and a propenyloxy group at the 3rd position of the indazole ring. It is known for its potential chemical reactivity and applications in various fields due to its unique structure.
Uses
Used in Chemical Synthesis:
1-BENZYL-3-PROPENYLOXY-1H-INDAZOLE is used as a chemical intermediate for the synthesis of various complex organic molecules. Its unique structure allows it to undergo specific chemical reactions, such as the Claisen rearrangement, which can lead to the formation of other valuable compounds like 1-benzyl-2-allyl-indazolin-3-one.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-BENZYL-3-PROPENYLOXY-1H-INDAZOLE may be used as a starting material or a building block for the development of new drugs. Its ability to undergo chemical transformations makes it a promising candidate for the creation of novel therapeutic agents with potential applications in various medical conditions.
Used in Material Science:
The compound may also find applications in the field of material science, where its unique structure and reactivity can be exploited to design and synthesize new materials with specific properties, such as improved stability, enhanced reactivity, or tailored physical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 25854-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,5 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25854-83:
(7*2)+(6*5)+(5*8)+(4*5)+(3*4)+(2*8)+(1*3)=135
135 % 10 = 5
So 25854-83-5 is a valid CAS Registry Number.
25854-83-5Relevant articles and documents
A MULTICORE CHEMICAL COMPOUND LIBRARY
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Page/Page column 50-61, (2010/02/15)
There is provided a method to convert O-functionalized indazolinone-derivatives to the corresponding N2-functinoalised indazolinone derivatives, by use of microwave energy or a transition metal catalyst. A preferred catalyst is palladium tetrakis. The method described allows the creation of a library of chemical compounds which can be screened for biological activity.
