163814-41-3 Usage
Uses
Used in Pharmaceutical Industry:
[S-(E)]-2-(methoxydiphenylmethyl)-1-(2-nitroethenyl)-pyrrolidine is used as a building block for the production of various pharmaceuticals due to its complex structure and potential pharmacological properties.
Used in Organic Synthesis:
In the field of organic synthesis, [S-(E)]-2-(methoxydiphenylmethyl)-1-(2-nitroethenyl)-pyrrolidine is used as a reagent, contributing to the creation of diverse chemical compounds.
Used in Antitumor Applications:
[S-(E)]-2-(methoxydiphenylmethyl)-1-(2-nitroethenyl)-pyrrolidine has been studied for its potential as an antitumor agent, making it a candidate for development in the area of cancer treatment.
Used in Antiviral Applications:
Additionally, [S-(E)]-2-(methoxydiphenylmethyl)-1-(2-nitroethenyl)-pyrrolidine has shown promise as an antiviral agent, indicating its potential use in the development of treatments for viral infections.
Used in Agrochemical Industry:
Its potential applications extend to the agrochemical industry, where it may be utilized as a component in the development of pesticides or other agricultural chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 163814-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,8,1 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 163814-41:
(8*1)+(7*6)+(6*3)+(5*8)+(4*1)+(3*4)+(2*4)+(1*1)=133
133 % 10 = 3
So 163814-41-3 is a valid CAS Registry Number.
163814-41-3Relevant academic research and scientific papers
Enantioselective creation of quaternary carbon centers through addition-elimination reaction: Asymmetric nitroolefination of 3-substituted 2-oxindoles
Fuji, Kaoru,Kawabata, Takeo,Ohmori, Toshiumi,Shang, Muhong,Node, Manabu
, p. 951 - 964 (2007/10/03)
Nitroolefination of 3-substituted 2-oxindoIes with nitroenamine (5) afforded the corresponding products having quaternary carbon centers with high ee in good yield. Application of this method to concise syntheses of (-)-esermethole (24) and (-)-pseudophrynaminol (28) is described.
An efficient asymmetric synthesis of nitroolefinic lactones with chiral nitroenamines possessing bulky chiral leaving groups
Yang, Xiaowu,Wang, Rui
, p. 3275 - 3281 (2007/10/03)
An efficient asymmetric nitroolefination of enolates 4a-c, 5 afforded multifunctional group nitroolefinic lactones 7a-e and 8a,b containing stereogenic quaternary carbon centers using bulky chiral nitroenamines 1a,b-3a,b as chiral auxiliaries. Studies on the effect of the bulkiness of leaving group showed that bulky nitroenamines la,b gave higher ees and yields than those of the less bulky 2a,b-3a,b. A possible cyclic transition model is proposed to elucidate the S selectivity.
