60329-10-4 Usage
Uses
Used in Organic Synthesis:
2,2,2-triphenyl-3-oxa-2lambda~5~-phosphabicyclo[3.1.0]hexane is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules.
Used in Catalysis:
In the field of catalysis, 2,2,2-triphenyl-3-oxa-2lambda~5~-phosphabicyclo[3.1.0]hexane is used as a catalyst or a catalyst precursor. Its phosphorus atom and the attached phenyl groups can interact with reactants, facilitating chemical reactions and improving reaction efficiency.
Used in Pharmaceutical Research:
2,2,2-triphenyl-3-oxa-2lambda~5~-phosphabicyclo[3.1.0]hexane is utilized in pharmaceutical research as a potential candidate for the development of new drugs. Its unique structure may offer novel pharmacological properties, contributing to the discovery of innovative therapeutic agents.
Used in Material Science Research:
In material science, 2,2,2-triphenyl-3-oxa-2lambda~5~-phosphabicyclo[3.1.0]hexane is employed in the study and development of new materials. Its unique structural features may contribute to the creation of advanced materials with specific properties for various applications.
Overall, 2,2,2-triphenyl-3-oxa-2lambda~5~-phosphabicyclo[3.1.0]hexane is a versatile compound with diverse potential applications across different industries, making it a valuable asset in the realm of scientific research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 60329-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,2 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 60329-10:
(7*6)+(6*0)+(5*3)+(4*2)+(3*9)+(2*1)+(1*0)=94
94 % 10 = 4
So 60329-10-4 is a valid CAS Registry Number.
60329-10-4Relevant academic research and scientific papers
Design of spiro[2.3]hex-1-ene, a genetically encodable double-strained alkene for superfast photoclick chemistry
Yu, Zhipeng,Lin, Qing
supporting information, p. 4153 - 4156 (2014/04/03)
Reactive yet stable alkene reporters offer a facile route to studying fast biological processes via the cycloaddition-based bioorthogonal reactions. Here, we report the design and synthesis of a strained spirocyclic alkene, spiro[2.3]hex-1-ene (Sph), for an accelerated photoclick chemistry, and its site-specific introduction into proteins via amber codon suppression using the wild-type pyrrolysyl-tRNA synthetase/tRNACUA pair. Because of its high ring strain and reduced steric hindrance, Sph exhibited fast reaction kinetics (k2 up to 34 000 M-1 s-1) in the photoclick chemistry and afforded rapid (10 s) bioorthogonal protein labeling.
Tertiary amine-triggered cascade SN2/cycloaddition: An efficient construction of complex azaheterocycles under mild conditions
Hu, Jian,Tian, Bing,Wu, Xinyan,Tong, Xiaofeng
supporting information, p. 5074 - 5077 (2013/01/15)
In this paper, an amine-triggered cascade SN2/cycloaddtion sequence between 2-(acetoxymethyl)buta-2,3-dienoate 1 and various π-system functionalized tosylamides 3 has been reported, which provides a facile method for stereoselective construction of structurally diverse azaheterocycles.
Bu2SnIH-promoted proximal bond cleavage of methylenecyclopropanes and successive radical cyclization and/or Pd-catalyzed coupling reaction
Hayashi, Naoki,Hirokawa, Yusuke,Shibata, Ikuya,Yasuda, Makoto,Baba, Akio
, p. 2912 - 2913 (2008/09/20)
The unprecedented regioselective hydrostannation of methylenecyclopropanes to give vinyltins was achieved using dibutyliodotin hydride (Bu2SnIH), which could be applied to intramolecular radical cyclization. Copyright
