1528-22-9 Usage
Uses
Used in Organic Synthesis:
Cyclobutane, (1-methylethylidene)is used as a key intermediate in organic synthesis for the production of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, such as Diels-Alder reactions, hydrogenation, and oxidation, enabling the synthesis of complex organic molecules.
Used in Materials Science:
In the field of materials science, Cyclobutane, (1-methylethylidene)is utilized for the development of novel materials with specific properties. Its ability to undergo polymerization and copolymerization reactions contributes to the creation of new polymeric materials with tailored characteristics, such as improved mechanical strength, thermal stability, and chemical resistance.
Used in Pharmaceutical Industry:
Cyclobutane, (1-methylethylidene)is employed as a building block in the synthesis of pharmaceutical compounds. Its reactive nature allows for the formation of diverse drug molecules with potential therapeutic applications. Researchers are exploring its use in the development of new drugs targeting various diseases and medical conditions.
Overall, Cyclobutane, (1-methylethylidene)is a versatile compound with a wide range of applications across different industries, including organic synthesis, materials science, and pharmaceuticals. Its unique structure and reactivity make it a valuable asset in the development of new compounds and materials with specific properties and functions.
Check Digit Verification of cas no
The CAS Registry Mumber 1528-22-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,2 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1528-22:
(6*1)+(5*5)+(4*2)+(3*8)+(2*2)+(1*2)=69
69 % 10 = 9
So 1528-22-9 is a valid CAS Registry Number.
1528-22-9Relevant academic research and scientific papers
Synthesis of tricyclopentanoid sesquiterpenes via rearrangement routes: (±)-modhephene, (±)-epimodhephene and (±)-isocomene
Fitjer, Lutz,Majewski, Marita,Monzo-Oltra, Honorato
, p. 8835 - 8852 (2007/10/03)
Based on model studies with dispiroundecane 10, dispiroundecane 1 has been synthesized and rearranged to (±)-modhephene 6 and (±)-isocomene 7. The epimeric dispiroundecane 9 yields (±)-epimodhephene 12. A total of thirteen rearrangement products (6, 7, 12, 37, 38, 39, 42, 44, 55, 57, 64, 67) have been isolated from 1 and/or 9, including six unnatural triquinanes. Two of these (55, 57) are formed by unusual 1,3- and 1,4-shifts, respectively. A mechanistic rationale on the basis of force field calculations is given.
