477199-85-2 Usage
Chemical class
Naphthalenes
It belongs to the class of naphthalenes, which are a group of organic compounds consisting of two fused benzene rings.
Dihydroxy derivative
Naphthalene
The compound is a dihydroxy derivative of naphthalene, meaning it has two hydroxyl (-OH) groups attached to the naphthalene structure.
Methoxy and methyl substituents
6-methoxy and 4,7-dimethyl
The compound has a methoxy (-OCH3) group at the 6th position and two methyl (-CH3) groups at the 4th and 7th positions.
Chiral molecule
(1R,2S,4R) designation
The compound is a chiral molecule, which means it has a specific stereochemical arrangement. The (1R,2S,4R) designation indicates the configuration of the chiral centers in the molecule.
Potential applications
Pharmaceuticals and organic synthesis
The compound has potential applications in various industries, including pharmaceuticals and organic synthesis, due to its unique structure and properties.
Research and development
Subject of interest
The unique structure and properties of 1,2-Naphthalenediol, 1,2,3,4-tetrahydro-6-methoxy-4,7-dimethyl-, (1R,2S,4R)(9CI) make it a subject of interest for further research and development in the fields of chemistry and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 477199-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,7,1,9 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 477199-85:
(8*4)+(7*7)+(6*7)+(5*1)+(4*9)+(3*9)+(2*8)+(1*5)=212
212 % 10 = 2
So 477199-85-2 is a valid CAS Registry Number.
477199-85-2Relevant academic research and scientific papers
Chemoenzymatic collective synthesis of optically active hydroxyl(methyl)tetrahydronaphthalene-based bioactive terpenoids
Batwal, Ramesh U.,Argade, Narshinha P.
, p. 11331 - 11340 (2015/11/27)
Starting from succinic anhydride and 2-methylanisole, a chemoenzymatic collective formal/total synthesis of several optically active tetrahydronaphthalene based bioactive natural products has been presented via advanced level common precursors; the natural product and antipode (-)/(+)-aristelegone B. Regioselective benzylic oxidations, stereoselective introduction of hydroxyl groups at the α-position of ketone moiety in syn-orientation, efficient enzymatic resolutions with high enantiomeric purity, stereoselective reductions, samarium iodide induced deoxygenations and tandem acylation-Wittig reactions without racemization and/or eliminative aromatization were the key features. An attempted diastereoselective synthesis of (±)-vallapin has also been described.
