502495-70-7 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 9 carbon (C) atoms, 14 hydrogen (H) atoms, and 2 oxygen (O) atoms.
2. Cycloalkanediol Compound
Explanation
This term refers to a type of organic compound that contains a cyclic structure (a ring) with two hydroxyl (OH) groups attached to the ring.
3. Two Double Bonds on the Cyclopentane Ring
Explanation
The cyclopentane ring in 1,3-Cyclopentanediol,2,4-diethenyl-,(1R,2S,3S,4S)-rel-(9CI) has two carbon-carbon double bonds (C=C), which are represented by the term "diethenyl."
Explanation
The stereo-specific configuration refers to the arrangement of atoms in three-dimensional space. In 1,3-Cyclopentanediol,2,4-diethenyl-,(1R,2S,3S,4S)-rel-(9CI), the (1R,2S,3S,4S)-rel configuration is the most stable, indicating the specific arrangement of the atoms at the numbered positions on the cyclopentane ring.
5. Used in Synthesis of Organic Compounds
Explanation
1,3-Cyclopentanediol,2,4-diethenyl-,(1R,2S,3S,4S)-rel-(9CI) serves as a starting material or intermediate in the synthesis of various organic compounds, which can be further modified or transformed into different molecules.
6. Building Block in Pharmaceutical Manufacturing
Stereo-specific Configuration
(1R,2S,3S,4S)-rel
Check Digit Verification of cas no
The CAS Registry Mumber 502495-70-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,2,4,9 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 502495-70:
(8*5)+(7*0)+(6*2)+(5*4)+(4*9)+(3*5)+(2*7)+(1*0)=137
137 % 10 = 7
So 502495-70-7 is a valid CAS Registry Number.
502495-70-7Relevant academic research and scientific papers
Synthesis of (polyfluoroalkyl)cyclopentenes as model compounds for fluorophilic cyclopentadienes
Kvicala, Jaroslav,Briza, Tomas,Paleta, Oldrich,Cermak, Jan
, p. 1345 - 1358 (2007/10/03)
Nucleophilic opening of the epoxide ring in 6-oxabicyclo[3.1.0]hexane (1) with ethenyl-magnesium bromide was employed for the preparation of 2-ethenylcyclopentan-1-ol (2). Radical addition of perfluoroalkyl iodides 3 to alcohol 2 afforded (polyfluoroiodoalkyl)cyclopentanols 4, which were deiodinated with tributylstannane to (polyfluoroalkyl)-cyclopentanols 5, followed by dehydration with Nafion-H to the target (polyfluoroalkyl)-cyclopentenes 6, which are potential intermediates for fluorous chemistry. Attempts to synthesize (polyfluoroalkyl)cyclopentadienes or bis(polyfluoroalkyl)cyclopentadienes failed due to the exclusive formation of unexpected side product, polyfluoroiodoalkanol 7, in the course of radical addition of perfluoroalkyl iodides 3 to ethenylcyclopentenol (8) or diethenylcyclopentanediol (9), respectively.
