CAS 18087-10-0

4,5-dimethyl-2-nitrophenol

Description:

4,5-Dimethyl-2-nitrophenol is an organic compound characterized by its aromatic structure, which includes a phenolic group substituted with two methyl groups and a nitro group. The presence of the nitro group introduces significant polarity and reactivity, making this compound a potential candidate for various chemical reactions, including electrophilic substitution. It typically appears as a solid at room temperature and is soluble in organic solvents, but its solubility in water is limited due to the hydrophobic methyl groups. The compound exhibits acidic properties due to the hydroxyl (-OH) group, which can donate a proton in solution. Its molecular structure contributes to its potential applications in the synthesis of dyes, pharmaceuticals, and agrochemicals. Additionally, 4,5-dimethyl-2-nitrophenol may pose environmental and health risks, necessitating careful handling and disposal. As with many nitrophenolic compounds, it may also exhibit toxicological effects, emphasizing the importance of safety measures in its use and study.

Formula: C₈H₉NO₃

InChI: InChI=1/C8H9NO3/c1-5-3-7(9(11)12)8(10)4-6(5)2/h3-4,10H,1-2H3

SMILES: Cc1cc(c(cc1C)O)N(=O)=O

Synonyms:

• Phenol, 4,5-dimethyl-2-nitro-
• 4,5-Dimethyl-2-nitrophenol
• 4,5-Dimethyl-2-hydroxynitrobenzene, 4-Hydroxy-5-nitro-o-xylene

4,5-Dimethyl-2-nitrophenol

CAS: 18087-10-0

Formula: C₈H₉NO₃

Purity: 97%

Molecular weight: 167.1620

Ref: IN-DA00KKAV

4,5-Dimethyl-2-nitrophenol

CAS: 18087-10-0

4,5-Dimethyl-2-nitrophenol

Purity: ≥95%

Color and Shape: Solid

Molecular weight: 167.16g/mol

Ref: 54-OR43630

4,5-Dimethyl-2-nitrophenol

CAS: 18087-10-0

Formula: C₈H₉NO₃

Purity: 97.0%

Color and Shape: Solid

Molecular weight: 167.164

Ref: 10-F068278

4,5-Dimethyl-2-nitrophenol

CAS: 18087-10-0

4,5-Dimethyl-2-nitrophenol is a phenolic compound that can be synthesized from a variety of precursors. It has been shown to react with hydrogen peroxide and chloride to produce nitrobenzene. Nitrobenzene has been used as an intermediate in the synthesis of other organic compounds. 4,5-Dimethyl-2-nitrophenol also reacts with hydrogen peroxide to form the fluorescent product 2,6-dichloro-4-(p-hydroxyphenyl)phenol. This reaction is used for detection of hydrogen peroxide in environmental chemistry. 4,5-Dimethyl-2-nitrophenol can undergo tautomeric shifts between its dienone and enedione forms. The ligand interactions of these two forms are different, which may lead to different reactions with other molecules.

Formula: C₈H₉NO₃

Purity: Min. 95%

Molecular weight: 167.16 g/mol

Ref: 3D-TAA08710