70452-32-3 Usage
Description
5-nitro-3-(2-oxo-2-phenylethylidene)-1,3-dihydro-2H-indol-2-one is a complex chemical compound that belongs to the class of nitro compounds. It features a nitro group and a 2-oxo-2-phenylethylidene group attached to a 1,3-dihydro-2H-indol-2-one ring system. This unique structure and the presence of various functional groups may endow it with potential applications in fields such as organic synthesis, medicinal chemistry, and material science.
Uses
Used in Organic Synthesis:
5-nitro-3-(2-oxo-2-phenylethylidene)-1,3-dihydro-2H-indol-2-one is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure and functional groups make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 5-nitro-3-(2-oxo-2-phenylethylidene)-1,3-dihydro-2H-indol-2-one is used as a potential lead compound for the development of new drugs. Its structural features and functional groups can be exploited to design and optimize molecules with specific biological activities, such as antimicrobial, antiviral, or anticancer properties.
Used in Material Science:
5-nitro-3-(2-oxo-2-phenylethylidene)-1,3-dihydro-2H-indol-2-one may also find applications in material science, where its unique structure and functional groups can be utilized to develop new materials with specific properties. These materials could have potential uses in various industries, such as electronics, coatings, or advanced materials for energy storage and conversion.
Further studies and research are needed to fully explore the potential uses and properties of 5-nitro-3-(2-oxo-2-phenylethylidene)-1,3-dihydro-2H-indol-2-one, as its complex structure and functional groups offer a wide range of possibilities in different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 70452-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,5 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70452-32:
(7*7)+(6*0)+(5*4)+(4*5)+(3*2)+(2*3)+(1*2)=103
103 % 10 = 3
So 70452-32-3 is a valid CAS Registry Number.
70452-32-3Relevant articles and documents
Phosphine-Catalyzed Interrupted Morita–Baylis–Hillman Reaction and Switchable Domino Reactions of α-Substituted Activated Olefins with Formaldehyde and Mechanism Elucidation
Gu, Jing,Xiao, Ben-Xian,Ouyang, Qin,Du, Wei,Chen, Ying-Chun
, p. 155 - 160 (2019/01/21)
3-Olefinic oxindoles can undergo interrupted Morita-Baylis-Hillman reaction with formaldehyde. Apart from the previous reported dephosphoration to access reductive aldol-type products, here we uncovered that completely different pathways were followed by tuning the substitutions of 3-olefinic oxindoles. In combination with formalin, an unexpected domino phosphorus-ylide formation, aldol-type addition, hemeacetal formation and O-substitution process was observed to produce 1,3-dioxolane derivatives. Moreover, a switchable sequence to produce formate derivatives via a key hydride transfer process was furnished by simply replacing formalin with paraformaldehyde. Density functional theory calculations were conducted to well elucidate the catalytic reaction mechanism.
Synthesis of 3-hydroxy-3-phenacyloxindole analogs
Popp,Donigan
, p. 519 - 520 (2007/10/08)
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