80656-12-8 Usage
Explanation
The compound is named based on its structure, which includes a cyclopentane ring with two carboxylic acid groups and two methyl ester groups in a trans configuration.
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), and oxygen (O) atoms in the compound, which are 9, 14, and 4, respectively.
Explanation
The compound's structure consists of a five-membered cyclopentane ring with two carboxylic acid groups (-COOH) and two methyl ester groups (-OCH3) attached to it. The methyl ester groups are positioned on opposite sides of the ring, indicating a trans configuration.
Explanation
The compound is a trans isomer, which means that the two methyl groups are on opposite sides of the cyclopentane ring, resulting in a specific arrangement of the atoms in the molecule.
Explanation
The compound contains two functional groups carboxylic acid (-COOH) and ester (-OCH3). These groups contribute to the compound's reactivity and properties.
Explanation
Due to its unique structure, the compound is used as a starting material for the synthesis of a wide range of organic compounds and pharmaceuticals.
Explanation
The compound's versatility in synthesis makes it a valuable precursor in the chemical industry for the production of various materials, including polymers, resins, and agricultural chemicals.
Explanation
As with many chemical compounds, 1,2-Cyclopentanedicarboxylic acid, dimethyl ester, trans-(+/-)can pose risks if not handled with care. It is essential to follow proper safety protocols and regulations when working with this compound to minimize potential hazards.
Explanation
The compound has a chiral center at the cyclopentane ring, which allows for the existence of different stereoisomers (enantiomers and diastereomers) with distinct spatial arrangements of atoms.
Explanation
The compound is likely to be soluble in organic solvents such as ethanol, methanol, and acetone due to its nonpolar nature and the presence of ester groups.
Structure
Cyclopentane ring with two carboxylic acid groups and two methyl ester groups in a trans configuration
Isomer
Trans isomer
Functional Groups
Carboxylic acid, ester
Applications
Building block in the synthesis of various organic compounds and pharmaceuticals
Industrial Applications
Precursor in the production of polymers, resins, and agricultural chemicals
Hazardous Nature
Potential hazards if not properly controlled and managed
Stereochemistry
Chiral center at the cyclopentane ring
Solubility
Soluble in organic solvents
Check Digit Verification of cas no
The CAS Registry Mumber 80656-12-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,5 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80656-12:
(7*8)+(6*0)+(5*6)+(4*5)+(3*6)+(2*1)+(1*2)=128
128 % 10 = 8
So 80656-12-8 is a valid CAS Registry Number.
80656-12-8Relevant articles and documents
Understanding the Structure–Polymerization Thermodynamics Relationships of Fused-Ring Cyclooctenes for Developing Chemically Recyclable Polymers
Sathe, Devavrat,Wang, Junpeng,Zhou, Junfeng
supporting information, p. 928 - 934 (2022/01/19)
Polymers that can be chemically recycled to their constituent monomers offer a promising solution to address the challenges in plastics sustainability through a circular use of materials. The design and development of monomers for next-generation chemical
Synthesis of Dimethyl 1,2-Cycloalkanedicarboxylates by Electrochemical Cyclization of Dimethyl α,α-Dibromoalkanedioates Using a Copper Anode
Tokuda, Masao,Hayashi, Atsushi,Suginome, Hiroshi
, p. 2590 - 2592 (2007/10/02)
The electrochemical cyclization of dimethyl α,α'-dibromoalkanedioates by making use of a platinum cathode and a copper anode in the presence of sodium iodide gave three- to six-membered dimethyl 1,2-cycloalkanedicarboxylates in good yields.
Preparation of Small Ring Carbocycles via Intramolecular Oxidative Coupling of Bisenolates Derived from α,ω-Diesters
Babler, James H.,Sarussi, Steven J.
, p. 3462 - 3464 (2007/10/02)
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