883278-65-7 Usage
Main properties
1. Chemical compound belonging to the class of naphthalenes
2. Molecular structure consisting of an allyl group, a benzyl ether group, and a methoxy group
3. Potential applications in organic synthesis and pharmaceuticals
4. Possible biological activities
5. Requires proper handling and storage protocols for safety
Specific content
1. Molecular formula: C19H18O2
2. Molecular weight: 278.34 g/mol
3. Structure: Allyl group and benzyl ether group attached to naphthalene ring with methoxy group at 5th position
4. Potential uses: Organic synthesis, pharmaceuticals
5. Safety precautions: Proper handling and storage protocols to prevent adverse effects
6. Further research needed to fully understand biological activities
Check Digit Verification of cas no
The CAS Registry Mumber 883278-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,2,7 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 883278-65:
(8*8)+(7*8)+(6*3)+(5*2)+(4*7)+(3*8)+(2*6)+(1*5)=217
217 % 10 = 7
So 883278-65-7 is a valid CAS Registry Number.
883278-65-7Relevant academic research and scientific papers
The enantioselective synthesis of elecanacin through an intramolecular naphthoquinone-vinyl ether photochemical cycloaddition
Nielsen, Linda B.,Wege, Dieter
, p. 868 - 876 (2007/10/03)
Elecanacin, an unusual cyclobuta-fused naphthalene-1,4-dione derivative isolated from the bulbs of Eleutherine Americana Merr. et Heyne (Iridaceae) has been obtained, together with its epimer isoelecanacin, by a 2 + 2 cycloaddition resulting from irradiation of 5-methoxy-2-(2-vinyloxypropyl)naphthalene-1,4- dione. The synthesis of enantiopure elecanacin starting with (R)-propylene oxide has established the absolute configuration of the natural product and has revealed that the sample isolated from the bulbs possessed an enantiomeric excess of only 14%. The Royal Society of Chemistry 2006.
