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2-((E)-2-Methoxy-2-phenyl-vinyl)-malonic acid diethyl ester is a complex organic compound with the molecular formula C18H20O6. It is a derivative of malonic acid, featuring a diethyl ester group and a vinyl moiety with a methoxy and phenyl substitution. 2-((E)-2-Methoxy-2-phenyl-vinyl)-malonic acid diethyl ester is characterized by its E-configuration, indicating the geometric arrangement of the double bond in the vinyl group. It is a colorless to pale yellow solid and is soluble in organic solvents. The compound is synthesized through a series of chemical reactions and is used in the preparation of various pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is important to handle 2-((E)-2-Methoxy-2-phenyl-vinyl)-malonic acid diethyl ester with care, as it may have potential health risks and should be used in accordance with proper safety protocols.

84199-19-9

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84199-19-9 Usage

Diethyl ester derivative

Malonic acid The compound is derived from malonic acid by attaching diethyl ester groups to the molecule.

Contains a vinyl group

(E)-2-Methoxy-2-phenyl-vinyl The compound has a vinyl group (C=C) attached to a methoxy and phenyl group, contributing to its reactivity and versatility in organic chemistry.

Contains a phenyl group

2-Phenyl The compound also has a phenyl group (a six-membered aromatic ring) attached to the vinyl group, which influences its chemical properties and reactivity.

Used in organic synthesis

As a reagent The compound is utilized as a reagent in the preparation and synthesis of various organic molecules.

Chemical reactions

Esterification, hydrolysis, and addition reactions The presence of the vinyl group allows the compound to undergo a range of chemical reactions, such as forming esters, breaking down into acids and alcohols, or undergoing addition reactions with other molecules.

Versatile compound

Organic chemistry Due to its ability to participate in various chemical reactions, the compound is considered versatile and valuable in the field of organic chemistry.

Specific properties and applications

Vary depending on the reaction or transformation The properties and applications of the compound can differ based on the particular reaction or transformation being studied, making it adaptable for various purposes in chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 84199-19-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,1,9 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84199-19:
(7*8)+(6*4)+(5*1)+(4*9)+(3*9)+(2*1)+(1*9)=159
159 % 10 = 9
So 84199-19-9 is a valid CAS Registry Number.

84199-19-9Downstream Products

84199-19-9Relevant academic research and scientific papers

REACTION OF ARYL CHROMIUM CARBENE COMPLEXES WITH ETHYL PROPIOLATE. A VERSATILE VINYL ETHER FORMATION

Yamashita, Ayako,Scahill, Terrence A.

, p. 3765 - 3768 (2007/10/02)

Arylmethoxychromium-carbene complexes reacted with ethyl propiolate in the presence of alcohol to form good yields of aryl vinyl ether derivatives of malonate.

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