130369-05-0 Usage
Uses
Used in Pharmaceutical Industry:
3-(Boc-amino)cyclobutanemethanol is utilized as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and the presence of the Boc protecting group make it an ideal candidate for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-(Boc-amino)cyclobutanemethanol serves as a vital component in the creation of complex molecules with pesticidal properties. Its ability to be easily modified and incorporated into larger structures allows for the design of novel agrochemicals with improved efficacy and selectivity.
Used in Drug Discovery:
3-(Boc-amino)cyclobutanemethanol is employed as a valuable tool in drug discovery, where its reactivity and structural features contribute to the development of new chemical entities with potential therapeutic benefits. The Boc protecting group enables selective reactions and the synthesis of diverse chemical libraries for screening and optimization.
Used in Material Science:
In the field of material science, 3-(Boc-amino)cyclobutanemethanol is used for the synthesis of advanced materials with unique properties. Its ability to form complex structures and participate in various chemical reactions makes it a promising candidate for the development of new materials with applications in various industries, such as electronics, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 130369-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,3,6 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 130369-05:
(8*1)+(7*3)+(6*0)+(5*3)+(4*6)+(3*9)+(2*0)+(1*5)=100
100 % 10 = 0
So 130369-05-0 is a valid CAS Registry Number.
130369-05-0Relevant academic research and scientific papers
Radical hydroxymethylation of alkyl iodides using formaldehyde as a C1 synthon
Caiger, Lewis,Constantin, Timothée,Douglas, James J.,Juliá, Fabio,Leonori, Daniele,Sheikh, Nadeem S.,Sinton, Conar
, p. 10448 - 10454 (2021/08/20)
Radical hydroxymethylation using formaldehyde as a C1 synthon is challenging due to the reversible and endothermic nature of the addition process. Here we report a strategy that couples alkyl iodide building blocks with formaldehyde through the use of photocatalysis and a phosphine additive. Halogen-atom transfer (XAT) from α-aminoalkyl radicals is leveraged to convert the iodide into the corresponding open-shell species, while its following addition to formaldehyde is rendered irreversible by trapping the transient O-radical with PPh3. This event delivers a phosphoranyl radical that re-generates the alkyl radical and provides the hydroxymethylated product.
?-LACTAMASE INHIBITOR AND USE THEREOF
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Paragraph 0217; 0218, (2020/12/10)
Provided are a β-lactamase inhibitor of formula (I), or an ester, a stereoisomer or a pharmaceutically acceptable salt thereof, and a method of preparing the same. Further provided is a pharmaceutical composition comprising the β-lactamase inhibitor of formula (I), or the ester, the stereoisomer or pharmaceutically acceptable salt thereof. In addition, the present invention relates to a method for treating diseases caused by bacterial infection, which comprises administering the β-lactamase inhibitor of formula (I), or the ester, the stereoisomer or the pharmaceutically acceptable salt thereof to a patient or a subject in need.
