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Phosphonic acid, phenyl-, di-2-propynyl ester is a chemical compound that belongs to the class of organophosphorus compounds. It is a clear, colorless liquid with a slightly fruity odor and a low water solubility. Phosphonic acid, phenyl-, di-2-propynyl ester is valued for its ability to protect metals from corrosion by forming a protective film on their surface. It is also used as a stabilizer in various chemical processes and as an intermediate in the production of other chemicals.

1779-32-4

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1779-32-4 Usage

Uses

Used in Corrosion Inhibition Applications:
Phosphonic acid, phenyl-, di-2-propynyl ester is used as a corrosion inhibitor for its ability to protect metals from corrosion by forming a protective film on their surface.
Used in Chemical Process Stabilization:
Phosphonic acid, phenyl-, di-2-propynyl ester is used as a stabilizer in various chemical processes to ensure the smooth and controlled progression of reactions.
Used in Chemical Production:
Phosphonic acid, phenyl-, di-2-propynyl ester is used as an intermediate in the production of other chemicals, contributing to the synthesis of a wide range of compounds.
It is important to handle Phosphonic acid, phenyl-, di-2-propynyl ester with care, as it is flammable and may pose a risk to human health and the environment if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 1779-32-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,7 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1779-32:
(6*1)+(5*7)+(4*7)+(3*9)+(2*3)+(1*2)=104
104 % 10 = 4
So 1779-32-4 is a valid CAS Registry Number.

1779-32-4Relevant academic research and scientific papers

CuAAC Synthesis and Anion Binding Properties of Bile Acid Derived Tripodal Ligands

Erzunov, Dmitry A.,Latyshev, Gennadij V.,Averin, Alexey D.,Beletskaya, Irina P.,Lukashev, Nikolay V.

, p. 6289 - 6297 (2015)

The copper-catalyzed azide-alkyne cycloaddition reaction was used for the preparation of a series of bis- and tris-3- and 24-5β-cholanetriazolyl derivatives of phosphorus acids, which contained anion-binding triazolium sites and hydrophobic cholane residues. The influence of the location of the triazolium moiety (in 3α-, 3β-position) on fluoride-ion complexation was investigated. The anion-binding properties of tris(triazolium) ligands were studied for a series of inorganic and organic anions and high complexation constants were observed with fluoride, hydrosulfate, and benzoate anions. A series of bile acid derived pincer and tripodal ligands that contain anion-binding triazolium and phosphoramide sites were prepared. These compounds efficiently bind inorganic and organic anions to give 1:2 ligand/anion complexes.

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