77887-88-8 Usage
Explanation
Different sources of media describe the Explanation of 77887-88-8 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. A cyclic ether is a type of organic compound that contains a ring of atoms with an oxygen atom in the ring.
3. The compound has a ring structure with 12 atoms.
4. The compound contains four oxygen atoms in its ring structure.
5. This is an alternative name for 1,4,7,10-Tetraoxacyclotridecan-12-ol, which is derived from its structure and properties.
6. The compound is used as a ligand, which is a molecule that binds to a central metal ion to form a complex.
7. The compound can form stable complexes with alkali metal cations, such as sodium and potassium.
8. The compound has a high selectivity for binding to sodium and potassium ions, meaning it preferentially forms complexes with these ions over other metal ions.
9. Due to its ability to selectively bind certain metal ions, 1,4,7,10-Tetraoxacyclotridecan-12-ol has a range of applications in various fields, including chemical synthesis, pharmaceuticals, and industrial processes.
Type of compound
Cyclic ether
Ring size
12-membered
Oxygen atoms
Four
Application
Macrocyclic ligand in coordination chemistry
Ability to complex
Alkali metal cations
Selectivity
High for sodium and potassium ions
Applications
Chemical synthesis, pharmaceutical, and industrial processes
Check Digit Verification of cas no
The CAS Registry Mumber 77887-88-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,8 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77887-88:
(7*7)+(6*7)+(5*8)+(4*8)+(3*7)+(2*8)+(1*8)=208
208 % 10 = 8
So 77887-88-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O5/c10-9-7-13-5-3-11-1-2-12-4-6-14-8-9/h9-10H,1-8H2
77887-88-8Relevant articles and documents
HIV PROTEASE INHIBITORS AND METHODS FOR USING
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Page/Page column 27, (2011/06/10)
Compounds that inhibit proteolytic enzymes of Human Immunodeficiency Virus (HIV) are described. Preparation of the inhibitors, pharmaceutical compositions containing them, and uses of the compounds or compositions for the treatment of HIV infections are also described.
MACROHETEROCYCLES. SYNTHESIS AND CYCLIZATION OF MONOGLYCIDYL ETHERS OF GLYCOLS
Shabanov, A. L.,Ismiev, I. I.,Magerramova, L. M.,Elchiev, A. B.
, p. 251 - 254 (2007/10/02)
The monoglycidyl ethers of mono-, di-, and triethylene glycols were syntesized.Their cyclization led to the formation of crown ethers containing a hydroxyl group in the polyether ring.The crown ethers are capable of dissolving the picrates of alkali metals and lithium chloride in chloroform.
