285-61-0 Usage
Uses
Used in Organic Synthesis:
2-Oxabicyclo[3.1.0]hexane is used as a key intermediate in organic synthesis for the production of various compounds due to its reactive functional groups and stable bicyclic structure.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-Oxabicyclo[3.1.0]hexane serves as a building block for the synthesis of diverse medicinal compounds, leveraging its unique molecular framework to create new drug candidates.
Used in Agrochemical Development:
2-Oxabicyclo[3.1.0]hexane is utilized in the development of agrochemicals, contributing to the creation of novel pesticides and other agricultural chemicals that can improve crop protection and yield.
Used in Material Science:
2-Oxabicyclo[3.1.0]hexane is studied for its potential applications in material science, particularly in the development of new polymers and materials that can benefit from its structural properties, such as rigidity and chemical stability.
Used in Industrial Applications:
Due to its solubility and physical properties, 2-Oxabicyclo[3.1.0]hexane finds use in various industrial applications where its chemical stability and reactivity are advantageous.
Check Digit Verification of cas no
The CAS Registry Mumber 285-61-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,8 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 285-61:
(5*2)+(4*8)+(3*5)+(2*6)+(1*1)=70
70 % 10 = 0
So 285-61-0 is a valid CAS Registry Number.
285-61-0Relevant academic research and scientific papers
Photochemistry of 3-Oxacycloalkenes
Inoue, Yoshihisa,Matsumoto, Naofumi,Hakushi, Tadao,Srinivasan, R.
, p. 2267 - 2272 (2007/10/02)
Direct and sensitized photolyses of 3-oxacycloalkenes 1a-c has been studied in n-pentane and in alkohols.In contrast to the photochemistry of cycloalkenes, the direct photolyses of 1a and 1b in pentane gave the products 2, 3, and 4, 5, respectively, which are derived from an allylic O-C bond cleavage.In addition, in the case of 1b, a small amount of the carbene-derived product 6 was also obtained.The seven-membered oxacycloalkene 1c gave no volatile product upon direct irradiation in pentane.Upon direct or sensitized photolyses in methanol, oxacycloalkenes 1b or 1cgave the adducts 7b,c as major products.Irrespective of the method of excitation, the yield of the adduct in the photolyses in a series of alcohols decreased with decreasing pK(a) value of the alcohol which can be explained in terms of the formation and subsequent trapping of the intermediate trans isomer 14 by the alcohol.These results can be rationalized in terms of the reactivities of the ?,?* and ?,?* states and the increased stability of the Rydberg state.
