CAS 7417-20-1

3,5-Dimethoxybenzeneethanol

Description:

3,5-Dimethoxybenzeneethanol, also known as 3,5-dimethoxyphenethyl alcohol, is an organic compound characterized by its aromatic structure and the presence of two methoxy groups (-OCH3) attached to a benzene ring at the 3 and 5 positions, along with an ethanol side chain. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic aromatic structure. The presence of methoxy groups enhances its electron-donating properties, which can influence its reactivity and interactions in various chemical environments. 3,5-Dimethoxybenzeneethanol may be utilized in organic synthesis, as a building block for pharmaceuticals, or in the development of fragrances and flavoring agents. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₁₀H₁₄O₃

InChI: InChI=1S/C10H14O3/c1-12-9-5-8(3-4-11)6-10(7-9)13-2/h5-7,11H,3-4H2,1-2H3

InChI key: InChIKey=UGODKVFPYBAMPX-UHFFFAOYSA-N

SMILES: C(CO)C1=CC(OC)=CC(OC)=C1

Synonyms:

• 2-(3,5-Dimethoxyphenyl)ethan-1-ol
• 3,5-Dimethoxybenzeneethanol
• 3,5-Dimethoxyphenethyl alcohol
• Benzeneethanol, 3,5-Dimethoxy-
• NSC 101853
• Phenethyl alcohol, 3,5-dimethoxy-
• 2-(3,5-Dimethoxyphenyl)ethanol

2-(3,5-Dimethoxyphenyl)ethanol

CAS: 7417-20-1

Formula: C₁₀H₁₄O₃

Purity: 95%

Color and Shape: Liquid

Molecular weight: 182.2164

Ref: IN-DA00FFH6

2-(3,5-Dimethoxyphenyl)ethanol

CAS: 7417-20-1

2-(3,5-Dimethoxyphenyl)ethanol

Purity: 95%

Molecular weight: 182.22g/mol

Ref: 54-OR1044653

3,5-Dimethoxyphenethyl alcohol

CAS: 7417-20-1

Formula: C₁₀H₁₄O₃

Purity: 95%

Molecular weight: 182.219

Ref: 10-F242536

2-(3,5-Dimethoxymethyl)ethanol

CAS: 7417-20-1

2-(3,5-Dimethoxymethyl)ethanol is a chemical compound that has been shown to have antiproliferative effects. It inhibits the growth of cells by binding to and inhibiting the activation of growth factor receptors. 2-(3,5-Dimethoxymethyl)ethanol is also a nitro derivative that can be reduced with sodium borohydride to form 3,5-dimethoxyacetophenone. This conversion is facilitated by the presence of an acid catalyst such as hydrochloric acid or acetic acid. The synthesis of 2-(3,5-dimethoxymethyl)ethanol has been shown to follow a functional theory whereby the reactant is converted into the product in one step with no intermediate compounds formed.

Formula: C₁₀H₁₄O₃

Purity: Min. 95%

Molecular weight: 182.22 g/mol

Ref: 3D-HAA41720