64954-45-6 Usage
General Description
1,3-Naphthalenediol,6,8-dimethoxy- is a chemical compound that belongs to the class of naphthalenediol derivatives. It is also known as dimethoxy naphthalene-diol. This chemical contains two methoxy groups and two hydroxy groups on the naphthalene ring. It is commonly used in organic synthesis and as a building block for the preparation of various pharmaceuticals and natural products. 1,3-Naphthalenediol,6,8-dimethoxy- has also shown potential antioxidant and anti-inflammatory activities, making it an interesting target for further research and development in the medical and pharmaceutical fields.
Check Digit Verification of cas no
The CAS Registry Mumber 64954-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,5 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64954-45:
(7*6)+(6*4)+(5*9)+(4*5)+(3*4)+(2*4)+(1*5)=156
156 % 10 = 6
So 64954-45-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O4/c1-15-9-4-7-3-8(13)5-10(14)12(7)11(6-9)16-2/h3-6,13-14H,1-2H3
64954-45-6Relevant articles and documents
Biosynthetically Guided Structure–Activity Relationship Studies of Merochlorin A, an Antibiotic Marine Natural Product
López-Pérez, Borja,Pepper, Henry P.,Ma, Rong,Fawcett, Benjamin J.,Pehere, Ashok D.,Wei, Qi,Ji, Zengchun,Polyak, Steven W.,Dai, Huanqin,Song, Fuhang,Abell, Andrew D.,Zhang, Lixin,George, Jonathan H.
, p. 1969 - 1976 (2017)
The onset of new multidrug-resistant strains of bacteria demands continuous development of antibacterial agents with new chemical scaffolds and mechanisms of action. We present the first structure–activity relationship (SAR) study of 16 derivatives of a s
Biomimetic total synthesis of (±)-merochlorina
Pepper, Henry P.,George, Jonathan H.
, p. 12170 - 12173 (2013)
Inspired: The proposed biosynthetic pathway toward the potent antibiotic meroterpenoid (±)-merochlorinA inspired its concise total synthesis. The key steps in the synthesis are a one-pot aromatization-alkylation reaction, followed by a biomimetic oxidativ
