119103-97-8 Usage
Description
(2E)-3-(4-isobutoxyphenyl)acrylic acid is a chemical compound with the molecular formula C13H16O3. It is classified as an acrylic acid derivative and belongs to the family of phenylacrylic acids. (2E)-3-(4-isobutoxyphenyl)acrylic acid is a white powder with a molecular weight of 220.26 g/mol. The presence of an isobutoxy group in its structure imparts certain properties and reactivity to the compound, making it useful in various chemical processes and applications.
Uses
Used in Pharmaceutical Industry:
(2E)-3-(4-isobutoxyphenyl)acrylic acid is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its unique structure and reactivity make it a valuable building block in the development of new pharmaceutical compounds.
Used in Organic Chemicals Industry:
(2E)-3-(4-isobutoxyphenyl)acrylic acid is used in the synthesis of organic chemicals, where its specific properties and reactivity contribute to the creation of a wide range of chemical products.
Used in Polymer Production:
(2E)-3-(4-isobutoxyphenyl)acrylic acid is used in the production of polymers, where it serves as a monomer or a building block for the development of specialized polymer materials with unique properties.
Used in Material Science:
(2E)-3-(4-isobutoxyphenyl)acrylic acid is used as a building block in the creation of specialized materials, where its isobutoxy group and reactivity contribute to the development of advanced materials with specific characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 119103-97-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,1,0 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 119103-97:
(8*1)+(7*1)+(6*9)+(5*1)+(4*0)+(3*3)+(2*9)+(1*7)=108
108 % 10 = 8
So 119103-97-8 is a valid CAS Registry Number.
119103-97-8Relevant articles and documents
Competitive formation of β-amino acids, propenoic, and ylidenemalonic acids by the Rodionov reaction from malonic acid, aldehydes, and ammonium acetate in alcoholic medium
Lebedev,Lebedeva,Sheludyakov,Kovaleva,Ustinova,Kozhevnikov
, p. 1113 - 1124 (2007/10/03)
The Rodionov reaction of 49 available aliphatic and aromatic aldehydes with malonic acid and ammonium acetate in alcoholic medium, resulting in formation of β-amino acids, propenoic, and ylidenemalonic acids, was studied. Certain regioselectivity regularities of the reaction were revealed. Among the variety of ketones studied, cyclohexanone is the only whose reaction yields a β-amino acid. Unusual dehydrofluorination of 6-chloro-2-fluorocinnamic acid under the Rodionov reaction was discovered. 2005 Pleiades Publishing, Inc.
