187528-21-8 Usage
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), and oxygen (O) atoms in a molecule of 1,2-Cyclopentanedimethanol,4,4-dimethoxy-,trans-(9CI), which is 9 carbon atoms, 18 hydrogen atoms, and 4 oxygen atoms.
Explanation
A diol is a type of alcohol that contains two hydroxyl (OH) groups. In this compound, the two hydroxyl groups are attached to the cyclopentane ring.
Explanation
The compound has two hydroxyl (OH) groups and two methoxy (CH3O) groups, which contribute to its chemical reactivity and properties.
Explanation
The core structure of the compound is a cyclopentane ring, which is a closed loop of five carbon atoms connected by bonds.
Explanation
The transdesignation in the compound's name indicates that the two methoxy groups are positioned on opposite sides of the cyclopentane ring, which affects its stereochemistry and potential applications.
Explanation
The compound may be used in various industrial and research applications, such as the synthesis of other organic compounds or as a building block for the production of polymers or resins.
Explanation
The purity of the compound can influence its specific properties and potential uses, as impurities may alter its reactivity, stability, or other characteristics.
Explanation
The compound is likely to be soluble in organic solvents, such as alcohols, ethers, and hydrocarbons, due to its nonpolar nature.
Explanation
The compound is generally stable under normal conditions, such as room temperature and pressure, but may decompose or react under extreme conditions, such as high temperatures or exposure to strong acids or bases.
Explanation
As with any chemical compound, it is essential to handle 1,2-Cyclopentanedimethanol,4,4-dimethoxy-,trans-(9CI) with care and follow appropriate safety guidelines to minimize risks to health and the environment.
Chemical Class
Diol
Functional Groups
Two hydroxyl groups and two methoxy groups
Cyclopentane Ring
Five-membered carbon ring
Trans-Configuration
Opposite sides of the cyclopentane ring
Industrial Applications
Synthesis of other organic compounds, building block for polymers or resins
Purity
Affects specific properties and potential uses
Solubility
Soluble in organic solvents
Stability
Stable under normal conditions
Safety
Handle with care, follow safety guidelines
Check Digit Verification of cas no
The CAS Registry Mumber 187528-21-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,5,2 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 187528-21:
(8*1)+(7*8)+(6*7)+(5*5)+(4*2)+(3*8)+(2*2)+(1*1)=168
168 % 10 = 8
So 187528-21-8 is a valid CAS Registry Number.
187528-21-8Relevant articles and documents
The Synthesis of Novel Trans-Oxabicyclo[3,3,0]octane Systems as Potential Inhibitors of HIV Protease
Mahler, Mikael E.,Palmer, Michael J.
, p. 193 - 194 (2007/10/03)
The novel trans-3-oxabicyclo[3,3.0]octan-7-one system has been prepared by intramolecular ring closure of the corresponding cyclopentane diol. Peralkylation and benzylidene substitution of the octanone has allowed the preparation of tetra-alkylated potential inhibitors of HIV protease. Weak activity against HIV protease (IC50's 70-100μM) was observed.
