CymitQuimica logo

CAS 10166-08-2

:

2-Methylbenzeneacetaldehyde

Description:
2-Methylbenzeneacetaldehyde, also known as o-tolualdehyde, is an aromatic aldehyde characterized by its structure, which features a methyl group and an aldehyde functional group attached to a benzene ring. This compound typically appears as a colorless to pale yellow liquid with a distinctive aromatic odor. It is soluble in organic solvents and has limited solubility in water. The presence of the aldehyde functional group makes it reactive, particularly in condensation reactions and as a potential electrophile in various organic syntheses. 2-Methylbenzeneacetaldehyde is used in the production of fragrances, flavoring agents, and as an intermediate in the synthesis of other organic compounds. Its chemical properties include a relatively low boiling point and a moderate vapor pressure, which can lead to volatility. Safety considerations include potential irritant effects on the skin and respiratory system, necessitating appropriate handling measures in laboratory and industrial settings. Overall, 2-Methylbenzeneacetaldehyde is an important compound in organic chemistry with various applications in the chemical industry.
Formula:C9H10O
InChI:InChI=1S/C9H10O/c1-8-4-2-3-5-9(8)6-7-10/h2-5,7H,6H2,1H3
InChI key:InChIKey=ACHWKVVBZRANAV-UHFFFAOYSA-N
SMILES:C(C=O)C1=C(C)C=CC=C1
Synonyms:
  • Acetaldehyde, o-tolyl-
  • 2-Methylbenzeneacetaldehyde
  • o-Tolylacetaldehyde
  • 2-TOLYLACETALDEHYDE
  • Benzeneacetaldehyde, 2-methyl-
  • (2-Methylphenyl)acetaldehyde
  • (2-Methylphenyl)acetaldehyde
Sort by

Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 1 products.
  • (2-Methylphenyl)acetaldehyde

    CAS:
    <p>(2-Methylphenyl)acetaldehyde is an enamine with a dimer. It can be used to synthesize amines and n-substituted amines. This compound has been shown to catalyze the dimerization of pinacolborane in the presence of protonation and deuterium activation. The regioselectivity of this reaction is dependent on the substituents on the 2-methylphenyl group. The reactivity of this compound is due to its ability to act as a nucleophile, which allows for reactions with electrophiles.</p>
    Formula:C9H10O
    Purity:Min. 95%
    Molecular weight:134.18 g/mol

    Ref: 3D-KAA16608

    1g
    967.00€
    100mg
    439.00€