77386-93-7 Usage
Molecular structure
Naphthalene-1,4-dione core with two hydroxyl groups at the 5 and 8 positions, and a tetrahydrofuran ring attached at the 2 position.
Synthetic compound
It is a human-made chemical with potential applications in pharmaceutical and material science research.
Potential applications
The compound has possible uses in drug discovery and development, as well as material science due to its unique structure and properties.
Antioxidant properties
The presence of hydroxyl groups in the molecule allows it to potentially neutralize free radicals and prevent oxidative damage.
Antibacterial properties
The compound may exhibit antibacterial activity, which could be useful in the development of new antibiotics and antimicrobial agents.
Stability
The unique structure of the tetrahydrofuran ring may provide the compound with increased stability, making it more suitable for use in various applications.
Reactivity
The specific structure of the compound may also contribute to its reactivity, which could be beneficial in chemical reactions and processes.
Further research needed
The precise chemical properties and potential applications of 2-(5,5-dimethyltetrahydrofuran-2-yl)-5,8-dihydroxynaphthalene-1,4-dione require additional investigation through research and experimentation to be fully understood and utilized.
Check Digit Verification of cas no
The CAS Registry Mumber 77386-93-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,8 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77386-93:
(7*7)+(6*7)+(5*3)+(4*8)+(3*6)+(2*9)+(1*3)=177
177 % 10 = 7
So 77386-93-7 is a valid CAS Registry Number.
77386-93-7Relevant articles and documents
SYNTHESIS OF SHIKALKIN AND CERTAIN RALATED COMPOUNDS
Novikov, V. L.,Balaneva, N. N.,Moiseenkov, A. M.,Elyakov, G. B.
, p. 1485 - 1494 (2007/10/02)
A successful total synthesis of a biologically active pigment from plants of the Boraginaceae family was carried out with naphthazarine as the starting material, and using the 1,4,5,8-tetramethoxynaphthalene, the corresponding 2-vinyl derivative and its epoxide or a cyclopropane adduct with diazoacetic ester at the key stages.In the course of developing the scheme of the synthesis of shikalkin, its three analogs were obtained, differing in the nature of the monoterpenoid side chain. Keywords: shikonin, alkannin, shikalkin, naphthazarine, tetramethoxynaphthalene, olefinization according to Wittig, cyclopropyl-carbinylic rearrangement, cerium-ammonium nitrate.
