41153-96-2 Usage
Description
1-(1,3-Dioxobutyl)pyrrolidine, also known as 4-(1,3-Dioxobutyl)pyrrolidine, is a synthetic chemical compound characterized by the molecular formula C8H13NO2. It features a cyclic amide structure with a butyrovalerone backbone and a pyrrolidine ring. 1-(1,3-Dioxobutyl)pyrrolidine is recognized for its potential applications in the pharmaceutical industry, particularly in drug development and the production of specific organic compounds. Its unique chemical structure and properties also suggest possible uses in medicine and biotechnology, although the specific applications may differ based on the context and industry.
Uses
Used in Pharmaceutical Industry:
1-(1,3-Dioxobutyl)pyrrolidine is used as a key intermediate in the synthesis of various pharmaceutical compounds due to its unique chemical structure. Its ability to form cyclic amides makes it a valuable building block for creating new drugs with potential therapeutic benefits.
Used in Organic Chemistry:
In the field of organic chemistry, 1-(1,3-Dioxobutyl)pyrrolidine serves as a versatile reagent and synthetic precursor for the production of specific organic compounds. Its butyrovalerone backbone and pyrrolidine ring contribute to its utility in creating a range of chemical products.
Used in Drug Development:
1-(1,3-Dioxobutyl)pyrrolidine is utilized as a research tool in the development of new drugs, where its unique properties can be harnessed to design and synthesize novel pharmaceutical agents. Its potential applications in this area are still being explored, and it may contribute to the discovery of innovative treatments for various medical conditions.
Used in Biotechnology:
Due to its distinctive chemical structure, 1-(1,3-Dioxobutyl)pyrrolidine may also find applications in the biotechnology sector. It could potentially be employed in the design of bioactive molecules, drug delivery systems, or as a component in the development of new biotechnological processes and products.
Check Digit Verification of cas no
The CAS Registry Mumber 41153-96-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,5 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41153-96:
(7*4)+(6*1)+(5*1)+(4*5)+(3*3)+(2*9)+(1*6)=92
92 % 10 = 2
So 41153-96-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO2/c1-7(10)6-8(11)9-4-2-3-5-9/h2-6H2,1H3
41153-96-2Relevant articles and documents
Improved synthesis of 3-aryl isoxazoles containing fused aromatic rings
Mirzaei, Yousef R.,Weaver, Matthew J.,Steiger, Scott A.,Kearns, Alison K.,Gajewski, Mariusz P.,Rider, Kevin C.,Beall, Howard D.,Natale
, p. 10360 - 10364 (2012)
A critical comparison of methods to prepare sterically hindered 3-aryl isoxazoles containing fused aromatic rings using the nitrile oxide cycloaddition (NOC) reveal that modification of the method of Bode, Hachisu, Matsuura, and Suzuki (BHMS), utilizing either triethylamine as base or sodium enolates of the diketone, ketoester, and ketoamide dipolarophiles, respectively, was the method of choice for this transformation.
Addition of Diazo Compounds ipso -C-H Bond to Carbon Disulfide: Synthesis of 1,2,3-Thiadiazoles under Mild Conditions
Zhang, Lei,Sun, Beiqi,Liu, Qianyi,Mo, Fanyang
supporting information, p. 4275 - 4278 (2018/04/14)
We describe here an operationally simple and straightforward synthesis method for a series of diverse 4,5-disubstituted 1,2,3-thiadiazoles via the nucleophilic addition of α-diazo carbonyl compounds to carbon disulfide. This method features using abundant and inexpensive carbon disulfide under mild reaction conditions.
Alpha-oxidation of amine derivatives by bis(2,2,2-tri-chloroethyl) azodicarboxylate and application of its products as iminium ion equivalents
Honzawa, Shinobu,Uchida, Mitsuaki,Tashiro, Takuya,Sugihara, Takumichi
, p. 994 - 1029 (2017/07/27)
Alpha-oxidation of amine derivatives by azodicarboxylate was examined. Among several azodicarboxylate esters and amides tested, bis(2,2,2-trichloroethyl) azodicarboxylate, that has highly electrophilic 2,2,2-trichloroethoxycarbonyl functional groups, was found to have excellent oxidation reactivity. Acylated or carbamoylated amines were suitable substrates for this reaction condition. Tertially amines could react in the same manner, but spontaneous elimination of hydrazinyl group occurred to give dimerized products. The reaction products were found to react with nucleophiles in the presence of Lewis or Br?nsted acid catalyst. This strongly suggests that the reaction products, alpha-hydrazinated amine derivatives, might serve as carbonyl group equivalents, very useful intermediates in synthetic organic chemistry.
