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2,2-Dichlor-3-phenyl-propionsaeure-methylester, also known as methyl 2,2-dichloro-3-phenylpropionate, is an organic compound with the chemical formula C10H10Cl2O2. It is a colorless to pale yellow liquid with a fruity odor. This ester is derived from propionic acid and phenol, featuring a methyl group attached to the propionic acid moiety, and two chlorine atoms on the same carbon atom. It is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and potential applications, it is important to handle 2,2-Dichlor-3-phenyl-propionsaeure-methylester with care, following proper safety protocols.

1552-80-3

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1552-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1552-80-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,5 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1552-80:
(6*1)+(5*5)+(4*5)+(3*2)+(2*8)+(1*0)=73
73 % 10 = 3
So 1552-80-3 is a valid CAS Registry Number.

1552-80-3Relevant academic research and scientific papers

Preparation of 2,2-Dihalocarboxylic Acid Methyl Esters by Oxidation-Chlorination of 2-(1-Haloalkyl)-4-methyl-1,3-dioxolanes with Trichloroisocyanuric Acid

Boni, Monica,Ghelfi, Franco,Pagnoni, Ugo Maria,Zucchi, Claudia

, p. 1622 - 1626 (1994)

Methyl 2,2-dichloro or 2-bromo-2-chloro carboxylates were obtained in excellent yields by oxidation-chlorination of 2-(1-haloalkyl)-4-methyl-1,3-dioxolanes with trichloroisocyanuric acid.

Trichloroisocyanuric Acid Oxidation of 2-Chloro Aldehyde Acetals to 2-Chloro Acids Esters

Boni, Monica,Ghelfi, Franco,Pagnoni, Ugo Maria,Pinetti, Adriano

, p. 156 - 159 (2007/10/02)

2-Chloro acid methyl esters were prepared in good yields treating 2-chloro aldehyde dimethyl acetals with trichloroisocyanuric acid in DMF.Aldehyde dimethyl acetals with the 2-halogen on a tertiary carbon atom were poorly reactive and could be oxidized efficiently only after their transformation into 1,3-dioxolanes.

ELECTROCHEMICAL CROSS-COUPLING OF ORGANIC HALIDES: TRICHLORMETHYLATION AND RELATED SYNTHESIS OF GEM-DICHLORO COMPOUNDS

Nedelec, J. Y.,Ait-Haddou-Mouloud, H.,Folest, J. C.,Perichon, J.

, p. 1699 - 1700 (2007/10/02)

The cross-coupling of activated alkyl halides with carbon tetrachloride or substituted trichloromethanes can be obtained electrochemically in good yield in an undivided cell with a sacrificial anode.

Electrochemical Cross-Coupling of Alkyl Halides in the Presence of a Sacrificial Anode

Nedelec, Jean-Yves,Mouloud, Hassan Ait Haddou,Folest, Jean-Claude,Perichon, Jacques

, p. 4720 - 4724 (2007/10/02)

The electrochemical trichloromethylation of various alkyl halides has been obtained in high yields in an undivided cell in the presence of a sacrificial anode.This cross-coupling process has been extended to the preparation of numerous gem-dichloro compounds from trichloro-substituted methanes and alkyl halides.Zinc,magnesium or aluminium were used as anodes according to the reduction potentiel of the reagents.Mixtures of polar aprotic solvents,e.g.THF-TMU or THF-NMP, were found more appropriate than pure solvents.The critical role of the metallic ions from the consumption of the anode has been clearly evidenced.

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