CAS 22633-33-6
:Methyl 2-hydroxy-3,5-dinitrobenzoate
Description:
Methyl 2-hydroxy-3,5-dinitrobenzoate, with the CAS number 22633-33-6, is an organic compound that belongs to the class of benzoates. It features a benzoic acid derivative structure, characterized by the presence of two nitro groups and a hydroxyl group on the aromatic ring, along with a methoxy group attached to the carboxylic acid. This compound is typically a yellow crystalline solid, indicating its potential for various applications in organic synthesis and as an intermediate in the production of dyes and pharmaceuticals. The presence of nitro groups contributes to its reactivity and potential use in nitration reactions. Methyl 2-hydroxy-3,5-dinitrobenzoate is also notable for its solubility in organic solvents, which facilitates its use in various chemical processes. However, due to the presence of nitro groups, it may pose certain hazards, including toxicity and environmental concerns, necessitating careful handling and disposal. Overall, this compound exemplifies the complexity and utility of nitro-substituted aromatic compounds in chemical research and industry.
Formula:C8H6N2O7
InChI:InChI=1S/C8H6N2O7/c1-17-8(12)5-2-4(9(13)14)3-6(7(5)11)10(15)16/h2-3,11H,1H3
InChI key:InChIKey=UMELTKSLWXJXNZ-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=C(O)C(N(=O)=O)=CC(N(=O)=O)=C1
Synonyms:- 2-Hydroxy-3,5-dinitro-benzoic acid methyl ester
- 3,5-Dinitro Salicylic Acid Methyl Ester
- Benzoic acid, 2-hydroxy-3,5-dinitro-, methyl ester
- Methyl 2-Hydroxy-3,5-Dinitrobenzoate
- NSC 203306
- Salicylic acid, 3,5-dinitro-, methyl ester
- Methyl 3,5-dinitrosalicylate
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Found 5 products.
methyl 2-hydroxy-3,5-dinitrobenzoate
CAS:Formula:C8H6N2O7Color and Shape:SolidMolecular weight:242.1424Methyl 3,5-dinitro-2-hydroxybenzoate
CAS:Methyl 3,5-dinitro-2-hydroxybenzoateFormula:C8H6N2O7Purity:≥95%Color and Shape: light yellow crystalline powderMolecular weight:242.14g/molMethyl 3,5-dinitrosalicylate
CAS:<p>Methyl 3,5-dinitrosalicylate is an efficient method for glycosylation of oligosaccharides. It is a stereoselective reaction that occurs in the presence of carbon disulphide as a solvent and topoisomerase as a catalyst. The reaction proceeds by nucleophilic attack of the glycosyl donor on the electrophilic nitro group of methyl 3,5-dinitrosalicylate to form a glycosyl-enzyme intermediate. This intermediate is then hydrolyzed to release an enzyme-bound sugar product. The reaction proceeds efficiently at room temperature and can be used in solid phase synthesis.</p>Formula:C8H6N2O7Purity:Min. 95%Color and Shape:PowderMolecular weight:242.14 g/molMethyl 3,5-Dinitrosalicylate
CAS:Controlled Product<p>Applications Derivative of Salicylic acid.<br></p>Formula:C8H6N2O7Color and Shape:NeatMolecular weight:242.17




