138760-34-6 Usage
Explanation
Different sources of media describe the Explanation of 138760-34-6 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 5 carbon atoms, 6 hydrogen atoms, 4 oxygen atoms, and 1 sulfur atom.
2. The compound has a cyclic structure, meaning its atoms are arranged in a closed loop or ring. It is a derivative of a sulfonic acid, which is a compound containing a sulfur atom bonded to three hydroxyl groups and one hydrogen atom.
3. The compound contains a five-membered ring composed of one sulfur atom and four other atoms (usually carbon and oxygen). In this case, the ring is an oxathiole, which is a combination of an oxide and a thiol (sulfur-hydrogen compound).
4. An oxo group (C=O) is a double-bonded oxygen atom. In this compound, the oxo group is attached to the second carbon atom in the five-membered ring.
5. A chelating agent is a compound that can form multiple bonds with a single metal ion, creating a stable complex. The presence of multiple functional groups in the compound allows it to act as a chelating agent.
6. Due to its unique chemical structure and properties, 1,3-OXATHIOLANE-2-CARBOXYLIC ACID, 5-OXOis used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals.
7. The compound's unique structure and properties make it a promising candidate for further research and development in the medical field, potentially leading to the discovery of new drugs and therapies.
8. The solubility of a compound refers to its ability to dissolve in a solvent, such as water or organic solvents. The material does not provide information on the solubility of 1,3-OXATHIOLANE-2-CARBOXYLIC ACID, 5-OXO-.
9. The stability of a compound refers to its resistance to decomposition or reaction under certain conditions. The material does not provide information on the stability of 1,3-OXATHIOLANE-2-CARBOXYLIC ACID, 5-OXO-.
Structure
Cyclic sulfonic acid derivative
Five-membered ring
1,3-oxathiole
Oxo group
Attached to the second carbon
Chelating agent
Can bind to metal ions
Applications
Pharmaceutical intermediates, agrochemicals, and specialty chemicals
Potential uses
Medical research and drug development
Solubility
Not specified in the material provided
Stability
Not specified in the material provided
Check Digit Verification of cas no
The CAS Registry Mumber 138760-34-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,7,6 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 138760-34:
(8*1)+(7*3)+(6*8)+(5*7)+(4*6)+(3*0)+(2*3)+(1*4)=146
146 % 10 = 6
So 138760-34-6 is a valid CAS Registry Number.
138760-34-6Relevant articles and documents
Processes for the diastereoselective separation of nucleoside analogue synthetic intermediates
-
, (2008/06/13)
The present invention relates to highly diastereoselective processes for production of cis-nucleosides and nucleoside analogues and derivatives in high optical purity and intermediates useful in those processes.
Synthesis of new 2,5-substituted 1,3-oxathiolanes. Intermediates in nucleoside chemistry
Kraus,Attardo
, p. 1046 - 1048 (2007/10/02)
A synthetic approach for new 2-hydroxymethyl-5-ethoxy-1,3-oxathiolane derivatives is described. These heterocyclic five membered rings are suitably substituted to be potential sugar candidates in nucleoside chemistry.
