188525-84-0 Usage
Explanation
The IUPAC name is a systematic method of naming chemical compounds. It provides a unique name for each chemical structure.
Explanation
The common name is a more informal and widely recognized name for a chemical compound, often used in place of the IUPAC name.
Explanation
The compound has a ring structure with five members (atoms), and two of these members are oxygen atoms, making it a heterocyclic structure.
Explanation
The compound is derived from dioxole, which is a five-membered heterocyclic structure containing two oxygen atoms.
Explanation
The compound is used as a building block for the synthesis of various compounds in organic synthesis and pharmaceutical research. It may also have potential applications in the fields of medicine and agriculture.
Explanation
Due to its chemical properties and potential uses, 1,3-dioxole-4-carboxylic acid, 5-(1-methylethyl)-2-oxo is considered an important compound for further research and development in various fields.
Structure
Five-membered heterocyclic structure containing two oxygen atoms
Derivative of Dioxole
Yes
Applications
Organic synthesis, pharmaceutical research, medicine, and agriculture
Importance
Important compound for further research and development
Check Digit Verification of cas no
The CAS Registry Mumber 188525-84-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,5,2 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 188525-84:
(8*1)+(7*8)+(6*8)+(5*5)+(4*2)+(3*5)+(2*8)+(1*4)=180
180 % 10 = 0
So 188525-84-0 is a valid CAS Registry Number.
188525-84-0Relevant academic research and scientific papers
A general synthesis of dioxolenone prodrug moieties
Sun, Chong-Qing,Cheng, Peter T.W.,Stevenson, Jay,Dejneka, Tamara,Brown, Baerbel,Wang, Tammy C.,Robl, Jeffrey A.,Poss, Michael A.
, p. 1161 - 1164 (2007/10/03)
A general method for the synthesis of dioxolenone prodrug moieties from appropriately substituted β-ketoesters is described. This novel and versatile sequence allows for the synthesis of alkyl- or aryl-substituted dioxolenone alcohols 8 or bromides 9. Coupling of the bromides 9 to prepare bis-dioxolenone phosphonate prodrug esters is also presented.
