301222-77-5 Usage
Uses
Used in Organic Synthesis:
4-(2-(1-ethoxy-1-oxopropan-2-ylidene)hydrazinyl)benzoic acid is used as a building block in organic synthesis for the formation of complex organic molecules, leveraging its unique structure and reactivity.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 4-(2-(1-ethoxy-1-oxopropan-2-ylidene)hydrazinyl)benzoic acid is used as a key intermediate in the development of new drugs, owing to its potential to be incorporated into medicinal compounds with therapeutic properties.
Used in Agrochemical Production:
4-(2-(1-ethoxy-1-oxopropan-2-ylidene)hydrazinyl)benzoic acid is utilized as a chemical component in the production of agrochemicals, where it may contribute to the creation of novel pesticides or other agricultural chemicals.
Used in Specialty Chemicals:
4-(2-(1-ethoxy-1-oxopropan-2-ylidene)hydrazinyl)benzoic acid is also used in the development of specialty chemicals, where its specific chemical properties can be harnessed for unique applications in various industries.
Used in Material Research and Development:
4-(2-(1-ethoxy-1-oxopropan-2-ylidene)hydrazinyl)benzoic acid may have potential applications in the research and development of new materials, where its chemical structure could be explored for innovative uses.
It is crucial to handle 4-(2-(1-ethoxy-1-oxopropan-2-ylidene)hydrazinyl)benzoic acid with care and adhere to safety protocols due to its potential hazardous properties if mishandled.
Check Digit Verification of cas no
The CAS Registry Mumber 301222-77-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,1,2,2 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 301222-77:
(8*3)+(7*0)+(6*1)+(5*2)+(4*2)+(3*2)+(2*7)+(1*7)=75
75 % 10 = 5
So 301222-77-5 is a valid CAS Registry Number.
301222-77-5Relevant academic research and scientific papers
Novel, selective indole-based ECE inhibitors: Lead optimization via solid-phase and classical synthesis
Brands, Michael,Ergueden, Jens-Kerim,Hashimoto, Kentaro,Heimbach, Dirk,Schroeder, Christian,Siegel, Stephan,Stasch, Johannes-Peter,Weigand, Stefan
, p. 4201 - 4205 (2007/10/03)
A novel class of indole-based endothelin-converting enzyme (ECE) inhibitors was identified by high throughput screening. We report systematic optimization of this compound class by means of classical and solid-phase chemistry. Optimized compounds with a bisarylamide side chain at the 2-position of the indole skeleton exhibit low-nanomolar activity on ECE.
Synthesis of Novel DNA Binding Agents: Indole-Containing Analogues of Bis-Netropsin
Khalaf, Abedawn I.,Pitt, Andrew R.,Suckling, Colin J.,Scobie, Martin,Urwin, John,Waigh, Roger D.,Fishleigh, Robert V.,Young, Stephen C.
, p. 751 - 770 (2007/10/03)
Molecular modelling studies showed that indole dicarboxylic acids are potential linkers for the synthesis of bis-netropsin analogues with a good fit to the minor groove of DNA. To test this hypothesis, 2-carboxyindole-6-acetic acid, indole-2,6-dicarboxyli
