CAS 5858-28-6

5-methyl-2-nitrobenzaldehyde

Description:

5-Methyl-2-nitrobenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with both a methyl group and a nitro group, as well as an aldehyde functional group. The presence of the nitro group introduces significant polarity and reactivity, making this compound a useful intermediate in various organic synthesis processes. It typically appears as a yellow to brown crystalline solid and has a distinct aromatic odor. The compound is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic aromatic structure. Its reactivity is influenced by the electron-withdrawing nature of the nitro group, which can participate in electrophilic aromatic substitution reactions. Additionally, 5-methyl-2-nitrobenzaldehyde can undergo reduction to yield corresponding amines or alcohols, and it may also participate in condensation reactions. Safety precautions should be taken when handling this compound, as nitro compounds can be hazardous and may pose environmental risks.

Formula: C₈H₇NO₃

InChI: InChI=1/C8H7NO3/c1-6-2-3-8(9(11)12)7(4-6)5-10/h2-5H,1H3

SMILES: Cc1ccc(c(c1)C=O)N(=O)=O

Synonyms:

• 5-Methyl-2-nitro-benzaldehyde
• Benzaldehyde, 5-methyl-2-nitro-

5-Methyl-2-nitrobenzaldehyde

CAS: 5858-28-6

Formula: C₈H₇NO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 165.1461

Ref: IN-DA00EBCT

5-Methyl-2-nitrobenzaldehyde

CAS: 5858-28-6

5-Methyl-2-nitrobenzaldehyde

Purity: 98%

Molecular weight: 165.15g/mol

Ref: 54-OR450028

5-Methyl-2-nitrobenzaldehyde

CAS: 5858-28-6

Formula: C₈H₇NO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 165.148

Ref: 10-F047928

5-Methyl-2-nitrobenzaldehyde

CAS: 5858-28-6

5-Methyl-2-nitrobenzaldehyde is an aldehyde that is used in the synthesis of other organic compounds. It can be prepared by reacting cinnamyl alcohol with pyridinium chlorochromate. 5-Methyl-2-nitrobenzaldehyde has been used as a natural antioxidant and in organic reactions. The yields are typically low, but the reaction can be improved by using inorganic reagents.

Formula: C₈H₇NO₃

Purity: Min. 95%

Molecular weight: 165.15 g/mol

Ref: 3D-FAA85828