39707-55-6 Usage
Structure
Benzenediol derivative with a naphthalenyl group
The compound is derived from benzenediol (hydroquinone) and contains a naphthalenyl group attached to it.
Chiral Center
Present
The compound has a chiral center, which means it can exist in different stereoisomers.
Stereochemistry
[1R-(1-alpha,-4]
The specific stereochemistry of the compound is designated as [1R-(1-alpha,-4], which describes the arrangement of atoms around the chiral center.
Synthesis
Through a series of chemical reactions
The compound is synthesized by undergoing a series of chemical reactions, which involve the formation and modification of its complex structure.
Industrial Applications
Pharmaceuticals, dyes, antioxidants, and other organic compounds
The compound is used in various industrial applications due to its unique structure and properties.
Properties
Depend on unique structure and composition
The specific properties of the compound, such as solubility, reactivity, and stability, depend on its complex structure and composition.
Molecular Weight
254.32 g/mol
The molecular weight is the sum of the atomic weights of all the atoms in the molecule.
Appearance
Solid or crystalline form
The compound is typically found in a solid or crystalline form, depending on the conditions.
Melting Point
Variable, depending on the specific stereoisomer
The melting point of the compound can vary depending on the stereochemistry of the molecule.
Boiling Point
Variable, depending on the specific stereoisomer
The boiling point of the compound can also vary depending on the stereochemistry of the molecule.
Density
Not readily available
The density of the compound is not readily available, as it may depend on the specific stereoisomer and conditions.
Solubility
Soluble in organic solvents
The compound is generally soluble in organic solvents, such as ethanol, methanol, and acetone, due to its nonpolar nature.
Reactivity
Reacts with various reagents to form different compounds
The compound can undergo various chemical reactions with different reagents, leading to the formation of new compounds with different properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 39707-55-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,0 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 39707-55:
(7*3)+(6*9)+(5*7)+(4*0)+(3*7)+(2*5)+(1*5)=146
146 % 10 = 6
So 39707-55-6 is a valid CAS Registry Number.
39707-55-6Relevant articles and documents
Total synthesis of yahazunol, zonarone and isozonarone
Laube, Thorsten,Schr?der, J?rg,Stehle, Ralf,Seifert, Karlheinz
, p. 4299 - 4309 (2007/10/03)
The synthesis of the marine natural products zonarone and isozonarone was achieved via (+)-albicanic acid, a sesquiterpene of the drimane type. Coupling of the appropiate drimane-synthon with lithiated hydroquinone ethers led to sesquiterpene arenes, which were further modified to the target molecules. Stereoselective epoxidation followed by regioselective opening of the oxirane ring yielded yahazunol.
