477338-25-3 Usage
Derivative of benzoic acid
2-(2-Bromo-acetyl)-4,5-dimethoxy-benzoic acid is derived from benzoic acid, which is a simple aromatic carboxylic acid.
Methoxy groups
Contains two -OCH3 groups These are electron-donating groups that can influence the reactivity and properties of the compound.
Bromo-acetyl group
It has a -COCH2Br group This functional group imparts unique reactivity and properties to the compound, making it useful in organic synthesis and pharmaceutical research.
Organic synthesis
2-(2-Bromo-acetyl)-4,5-dimethoxy-benzoic acid is commonly used as a reagent in the preparation of other organic compounds, making it a valuable building block in organic chemistry.
Pharmaceutical research
The compound has potential biological activity, which makes it useful in the development of novel drugs and pharmaceuticals.
Varying applications
The precise uses and applications of 2-(2-Bromo-acetyl)-4,5-dimethoxy-benzoic acid may vary depending on the specific research or industrial purpose, highlighting its versatility in different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 477338-25-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,7,3,3 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 477338-25:
(8*4)+(7*7)+(6*7)+(5*3)+(4*3)+(3*8)+(2*2)+(1*5)=183
183 % 10 = 3
So 477338-25-3 is a valid CAS Registry Number.
477338-25-3Relevant academic research and scientific papers
Palladium-catalyzed synthesis of o-acetylbenzoic acids: A new, efficient general route to 2-hydroxy-3-phenyl-1,4-naphthoquinones and indolo[2,3-b]naphthalene-6,11-diones
Barcia, José C,Cruces, Jacobo,Estévez, Juan C,Estévez, Ramón J,Castedo, Luis
, p. 5141 - 5144 (2007/10/03)
We describe here a new, efficient general synthesis of o-acetylbenzoic acids by Heck palladium-catalyzed arylation of n-butyl vinyl ether with o-bromobenzoic acid esters and the use of these compounds as starting materials for the synthesis of 3-benzylideneisochroman-1,4-diones, which readily rearrange to 2-hydroxy-3-phenyl-1,4-naphthoquinones. The application of this strategy to the synthesis of indolo[2,3-b]naphthalene-6,11-diones is also described.
