76669-83-5 Usage
Diol
Contains two hydroxyl (OH) groups
Derived from naphthalene
A polycyclic aromatic hydrocarbon
Hexahydro
Contains six hydrogen atoms in its structure
Physical State
Colorless solid
Building block
Used in the synthesis of various organic compounds
Industrial and research applications
Due to its chemical properties and molecular structure
Esterification
Can react with acids to form esters
Etherification
Can react with other alcohols to form ethers
Solubility
Generally soluble in organic solvents, such as ethanol, methanol, and acetone
Stability
Stable under normal conditions, but may decompose upon exposure to heat or strong acids/bases
Handling
Use proper protective equipment, such as gloves and eye protection, when handling this compound
Toxicity
Limited information available, but should be treated with caution due to its chemical reactivity and potential for decomposition products
Storage
Store in a cool, dry, and well-ventilated area, away from heat and strong acids/bases
Environmental Impact
Potentially harmful to aquatic life and should be disposed of according to local regulations and guidelines
Check Digit Verification of cas no
The CAS Registry Mumber 76669-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,6 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76669-83:
(7*7)+(6*6)+(5*6)+(4*6)+(3*9)+(2*8)+(1*3)=185
185 % 10 = 5
So 76669-83-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O2/c11-9-5-1-2-6-10(9,12)8-4-3-7-9/h1-4,11-12H,5-8H2
76669-83-5Relevant articles and documents
Conceptualization and Synthesis of the First Inosito-Inositol (Decahydroxydecalin, DHD): In silico Binding to β-Amyloid Protein
Bhat, Bilal A.,Mehta, Goverdhan,Rashid, Showkat
, p. 17005 - 17010 (2020)
Previously unknown entities in the form of 1,2,3,4,5,6,7,8,9,10-decahydroxydecalins (DHDs) have been conceptualized and the first member of this class, an inosito-inositol, has been synthesized from aromatic hydrocarbon naphthalene following a flexible strategy that is amenable to diversity creation. The DHD accessed here has been subjected to preliminary in silico evaluation with Aβ and may hold some promise in Alzheimer's disease therapeutics.
