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Phloroglucinol, 2,2-methylenebis(4,6-diacetyl-), also known as 2,2'-methylenebis(4,6-diacetylphloroglucinol) or 2,2'-Methylenebis(4,6-diacetyl-phloroglucinol), is a complex organic compound with the chemical formula C16H14O8. It is a derivative of phloroglucinol, a trihydroxybenzene compound, with two acetyl groups attached to each of the hydroxyl groups and a methylene bridge connecting the two phloroglucinol units. Phloroglucinol, 2,2-methylenebis(4,6-diacetyl- is known for its antioxidant properties and is used in various applications, including as a stabilizer for polymers and as a flame retardant. It is also found in some natural products and has been studied for its potential biological activities. The compound is characterized by its ability to form chelate complexes with metal ions, which contributes to its utility in various industrial and chemical processes.

726-28-3

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726-28-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 726-28-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 726-28:
(5*7)+(4*2)+(3*6)+(2*2)+(1*8)=73
73 % 10 = 3
So 726-28-3 is a valid CAS Registry Number.

726-28-3Relevant academic research and scientific papers

Pushing back the limits of hydrosilylation: Unprecedented catalytic reduction of organic ureas to formamidines

Pouessel, Jacky,Jacquet, Olivier,Cantat, Thibault

, p. 3552 - 3556 (2014/01/06)

Pushing back the limits: A novel catalytic transformation has been designed to prepare formamidine derivatives by reduction of substituted ureas with hydrosilanes. Simple iron catalysts based on commercially available iron salts and phosphine ligands prov

O-Iodoxybenzoic acid mediated oxidative desulfurization of 1,3-disubstituted thioureas to carbodiimides

Chaudhari, Pramod S.,Dangate, Prasad S.,Akamanchi, Krishnacharya G.

supporting information; experimental part, p. 3065 - 3067 (2011/02/25)

An efficient and mild oxidative desulfurization procedure using o-iodoxybenzoic acid has been developed for the synthesis of carbodiimides starting from easily synthesizable 1,3-disubstituted thioureas.

Copper(II) acetate/oxygen-mediated nucleophilic addition and intramolecular C-H activation/C-N or C-C bond formation: One-pot synthesis of benzimidazoles or quinazolines

He, Hua-Feng,Wang, Zhi-Jing,Bao, Weiliang

supporting information; experimental part, p. 2905 - 2912 (2010/12/29)

Diarylcarbodiimides or benzylphenylcarbodiimides are converted to 1,2-disubstituted benzimidazoles or 1,2-disustituted quinazolines via addition/intramolecular C-H bond activation/C-N or C-C bond forming reaction using copper(II) acetate/oxygen [Cu(OAc)2/O2] as the oxidant at 100°C in one-pot cascade procedure. Copyright

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