CAS 7287-82-3
:1-(2-Methylphenyl)ethanol
Description:
1-(2-Methylphenyl)ethanol, also known as o-cresol phenethyl alcohol, is an organic compound characterized by its aromatic structure and alcohol functional group. It features a phenyl ring substituted with a methyl group at the ortho position and a hydroxyl group (-OH) attached to an ethyl side chain. This compound is typically a colorless to pale yellow liquid with a sweet, floral odor, making it of interest in the fragrance and flavor industries. It is moderately soluble in water and more soluble in organic solvents, reflecting its amphiphilic nature. The presence of the hydroxyl group contributes to its reactivity, allowing it to participate in various chemical reactions, such as esterification and oxidation. Additionally, 1-(2-Methylphenyl)ethanol can exhibit biological activity, which may include antimicrobial properties. Safety data indicates that, like many organic solvents, it should be handled with care to avoid skin and eye irritation. Overall, its unique structure and properties make it a valuable compound in both industrial and research applications.
Formula:C9H12O
InChI:InChI=1S/C9H12O/c1-7-5-3-4-6-9(7)8(2)10/h3-6,8,10H,1-2H3
InChI key:InChIKey=SDCBYRLJYGORNK-UHFFFAOYSA-N
SMILES:C(C)(O)C1=C(C)C=CC=C1
Synonyms:- AI3-21992
- alpha-2-Dimethylbenzyl alcohol
- α,2-Dimethylbenzyl alcohol
- Benzyl alcohol, o,α-dimethyl-
- Benzenemethanol, alpha,2-dimethyl-
- 1-(2-Methylphenyl)ethanol
- Benzenemethanol, α,2-dimethyl-
- α,2-Dimethylbenzenemethanol
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Found 4 products.
1-(2-Methylphenyl)ethanol
CAS:Formula:C9H12OPurity:98%Color and Shape:LiquidMolecular weight:136.19101-(2-Methylphenyl)ethanol
CAS:<p>1-(2-Methylphenyl)ethanol is a colorless liquid with a pleasant odor. It can be used as an intermediate in the synthesis of various pharmaceuticals, such as diazepam and lorazepam. 1-(2-Methylphenyl)ethanol is oxidized to produce toxic metabolites that have been shown to have cytotoxic effects on mitochondria. In addition, 1-(2-Methylphenyl)ethanol has been shown to inhibit the formation of cyclic amides from carboxylic acids and amines by competing for the same enzyme binding site. The toxicity of this compound was studied in rats using acute toxicity tests, and it induced hematological parameters indicative of renal toxicity.</p>Formula:C9H12OPurity:Min. 95%Molecular weight:136.19 g/mol



