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680219-93-6

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680219-93-6 Usage

Chemical structure

A derivative of glycerol with two ethoxy tetrahydro-2H-pyran groups and one benzyl group attached to the glycerol backbone.

Functional groups

Contains ether, alcohol, and benzyl functional groups.

Molecular weight

Approximately 430.59 g/mol

Appearance

Likely a colorless to pale yellow liquid or solid, depending on the purity and concentration.

Solubility

Soluble in organic solvents such as ethanol, methanol, and dichloromethane.

Stability

Stable under normal temperature and pressure conditions, but sensitive to heat, light, and moisture.

Reactivity

Can undergo various chemical reactions, such as substitution, elimination, and oxidation reactions, due to the presence of multiple functional groups.

Applications

Commonly used as a reagent for organic synthesis, particularly in the field of organic chemistry and pharmaceuticals.

Potential uses

Has potential applications in the production of medications and other biologically active molecules, as well as in the development of new chemical compounds with potential therapeutic benefits.

Safety precautions

Should be handled with care, as it may be harmful if swallowed, inhaled, or comes into contact with the skin. Proper protective equipment, such as gloves and eye protection, should be used when handling this compound.

Storage

Should be stored in a cool, dry place, away from heat, light, and moisture, and in a sealed container to maintain its stability and purity.

Check Digit Verification of cas no

The CAS Registry Mumber 680219-93-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,0,2,1 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 680219-93:
(8*6)+(7*8)+(6*0)+(5*2)+(4*1)+(3*9)+(2*9)+(1*3)=166
166 % 10 = 6
So 680219-93-6 is a valid CAS Registry Number.

680219-93-6Relevant articles and documents

Synthesis of cationic cardiolipin analogues

Kasireddy, Krishnudu,Ali, Shoukath M.,Ahmad, Moghis U.,Choudhury, Sreeti,Chien, Pei-Yu,Sheikh, Saifuddin,Ahmad, Imran

, p. 345 - 362 (2008/02/01)

An approach was developed to synthesize a new class of cationic cardiolipin analogues containing two quaternary ammonium groups with tetra alkyl groups retaining "glycerol" moiety, the central core of the molecule. Cationic cardiolipin analogues were modified via introduction of either two or four oxyethylene groups to enhance the solubility in polar solvents. These newly synthesized cationic cardiolipin analogues can be applied to a broad range of drug delivery systems such as transfection reagents.

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