271794-66-2 Usage
Uses
Used in Organic Synthesis:
Benzyl2-chloro-2-[2-(4-methylphenyl)hydrazono]acetate is used as a reagent in organic synthesis for various chemical reactions. Its chloro and hydrazone functional groups make it a versatile building block for the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Benzyl2-chloro-2-[2-(4-methylphenyl)hydrazono]acetate is used for the synthesis of new potential drug candidates. Its unique structure and functional groups contribute to the development of innovative therapeutic agents.
Used in Medicinal Chemistry:
Due to its hydrazone functional group, Benzyl2-chloro-2-[2-(4-methylphenyl)hydrazono]acetate may have potential applications in the field of medicinal chemistry. It could be explored as an anti-inflammatory and anti-cancer agent, given the known biological activities of hydrazone-containing compounds.
Used in Research:
Benzyl2-chloro-2-[2-(4-methylphenyl)hydrazono]acetate is also used in research settings to study its chemical properties, reactivity, and potential applications in various chemical and biological processes.
It is important to handle Benzyl2-chloro-2-[2-(4-methylphenyl)hydrazono]acetate with care, as it may have toxic or hazardous properties. Proper safety measures should be taken during its synthesis, storage, and use to minimize any potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 271794-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,1,7,9 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 271794-66:
(8*2)+(7*7)+(6*1)+(5*7)+(4*9)+(3*4)+(2*6)+(1*6)=172
172 % 10 = 2
So 271794-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H15ClN2O2/c1-12-7-9-14(10-8-12)18-19-15(17)16(20)21-11-13-5-3-2-4-6-13/h2-10,18H,11H2,1H3/b19-15+
271794-66-2Relevant academic research and scientific papers
Nitrilimine cycloadditions onto partially saturated furo[3,4- c]thieno[2,3-d]pyrazoles. A problem in site selectivity
Broggini, Gianluigi,Garanti, Luisa,Molteni, Giorgio,Zecchi, Gaetano
, p. 917 - 927 (2007/10/03)
Partially saturated furo[3,4-c]thieno[2,3-d]pyrazoles (7-10) have been submitted to 1,3-dipolar cycloaddition with a variety of nitrilimines. The competitive formation of products due to the dipolar attack at different dipolarophilic sites has been observed. The experimental evidence is discussed by taking into account electronic features of the reactive species as well as their steric encumbrance.
