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2-(2,6-dichlorophenyl)-4-methacryloyloxymethyl-1,3-dioxolane is a complex organic compound with the molecular formula C12H12Cl2O4. It is characterized by a 1,3-dioxolane ring, which is a five-membered cyclic ether, and a methacryloyloxymethyl group attached to the 4-position. The 2,6-dichlorophenyl group is attached to the 2-position of the dioxolane ring, providing the molecule with two chlorine atoms at the 2 and 6 positions of the phenyl ring. This chemical is known for its use as a monomer in the production of polymers, particularly in the field of coatings and adhesives, due to its ability to form strong, durable materials. The presence of the dichlorophenyl group contributes to the chemical's stability and resistance to degradation, while the methacryloyloxymethyl group allows for polymerization with other monomers to create versatile polymeric materials.

78830-77-0

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78830-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78830-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,3 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78830-77:
(7*7)+(6*8)+(5*8)+(4*3)+(3*0)+(2*7)+(1*7)=170
170 % 10 = 0
So 78830-77-0 is a valid CAS Registry Number.

78830-77-0Downstream Products

78830-77-0Relevant academic research and scientific papers

1,3-Dioxolane Bearing Perfume and Herbicide Aldehyde Residues

Kamogawa, Hiroyoshi,Haramoto, Yuichiro,Nakazawa, Terumi,Sugiura, Harumitsu,Nanasawa, Masato

, p. 1577 - 1578 (2007/10/02)

4-Methacryloyloxymethyl-1,3-dioxolanes substituted at the 2 position with perfume and herbicide aldehyde residues were synthesized either by acetalization or by transacetalization involving 2,3-dihydroxypropyl methacrylate.The effect of the 2-substituent of the dioxolane ring on the rate of hydrolysis was remarkable.

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