103004-14-4 Usage
Explanation
Different sources of media describe the Explanation of 103004-14-4 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 6 carbon (C), 10 hydrogen (H), 3 oxygen (O), and 1 sulfur (S) atoms.
2. The compound has a ring-like structure formed by the atoms in the molecule, which is a common feature in many organic compounds.
3. The compound contains a sulfur atom, which is an important feature for its chemical properties and potential applications.
4. The carboxylic acid group (-COOH) is a functional group that gives the compound acidic properties and can participate in various chemical reactions.
5. The cis configuration indicates that the methyl group (-CH3) and the carboxylic acid group are on the same side of the cyclic structure. This arrangement can affect the compound's properties and potential applications.
6. Due to its cyclic structure and the presence of a carboxylic acid group, the compound may have potential applications in the pharmaceutical industry. However, further research and testing are required to determine its specific uses.
7. Before the compound can be used in any applications, it needs to undergo further research and testing to determine its properties, stability, and potential effects on biological systems.
Structure
Cyclic organic compound
Sulfur atom
Present
Carboxylic acid group
Present
Configuration
cis
Potential applications
Pharmaceutical industry
Research and testing
Required
Check Digit Verification of cas no
The CAS Registry Mumber 103004-14-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,0,0 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 103004-14:
(8*1)+(7*0)+(6*3)+(5*0)+(4*0)+(3*4)+(2*1)+(1*4)=44
44 % 10 = 4
So 103004-14-4 is a valid CAS Registry Number.
103004-14-4Relevant articles and documents
Resolution, Absolute Configuration, and Cholinergic Enantioselectivity of (+)- and (-)-cis-2-Methyl-5--1,3-oxathiolane Methiodide
Teodori, Elisabetta,Gualtieri, Fulvio,Angeli, Piero,Brasili, Livio,Giannella, Mario,Pigini, Maria
, p. 1610 - 1615 (2007/10/02)
The potent cholinergic agonist (+/-)-cis-2-methyl-5--1,3-oxathiolane methiodide was resolved into enantiomeric forms.Their absolute configurations were established by a synthetic pathway that also allowed the synthesis of the corresponding diastereomeric (+)- and (-)-trans-2-methyl-5--1,3-oxathiolane methiodide .Compound (+)-1, which is the most potent of the four isomers, showed the same absolute configuration as L-(+)-muscarine and (+)-cis-dioxolane.The four isomers were tested on guinea pig ileum and frog rectus abdominis, and their muscarinic and nicotinic potency (EPMR) and selectivity were determined.The relationships between stereoisomerism and potency are discussed.
