2529-39-7 Usage
Derivative of benzoic acid
2,3,4,5-tetramethylbenzoic acid is derived from benzoic acid, which is a simple aromatic carboxylic acid.
Four methyl groups
This compound is characterized by the presence of four methyl groups attached to the benzene ring, which gives it a tetramethyl-substituted structure.
Use as an intermediate
2,3,4,5-tetramethylbenzoic acid is primarily used as an intermediate in the synthesis of various organic compounds.
Applications in dyes, pharmaceuticals, and fragrances
The compound is used in the production of dyes, pharmaceuticals, and fragrances due to its chemical properties and reactivity.
Reagent in organic synthesis reactions
2,3,4,5-tetramethylbenzoic acid is suitable for use as a reagent in organic synthesis reactions, helping to create more complex molecules.
Building block for complex molecules
The compound serves as a building block for the creation of more complex molecules, making it a valuable component in organic chemistry.
Potential applications in polymer and resin materials
Due to its unique structure and reactivity, 2,3,4,5-tetramethylbenzoic acid has potential applications in the production of polymer and resin materials.
Check Digit Verification of cas no
The CAS Registry Mumber 2529-39-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,2 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2529-39:
(6*2)+(5*5)+(4*2)+(3*9)+(2*3)+(1*9)=87
87 % 10 = 7
So 2529-39-7 is a valid CAS Registry Number.
2529-39-7Relevant articles and documents
Twist does a twist to the reactivity: Stoichiometric and catalytic oxidations with twisted tetramethyl-IBX
Moorthy, Jarugu Narasimha,Senapati, Kalyan,Parida, Keshaba Nanda,Jhulki, Samik,Sooraj, Kunnikuruvan,Nair, Nisanth N.
, p. 9593 - 9601 (2012/01/03)
The methyl groups in TetMe-IBX lower the activation energy corresponding to the rate-determining hypervalent twisting (theoretical calculations), and the steric relay between successive methyl groups twists the structure, which manifests in significant solubility in common organic solvents. Consequently, oxidations of alcohols and sulfides occur at room temperature in common organic solvents. In situ generation of the reactive TetMe-IBX from its precursor iodo-acid, i.e., 3,4,5,6-tetramethyl-2-iodobenzoic acid, in the presence of oxone as a co-oxidant facilitates the oxidation of diverse alcohols at room temperature.
