5379-19-1

Basic information

• Product Name: 1-(2,4-DIMETHYLPHENYL)ETHANOL
• Synonyms: 1-(2,4-DIMETHYLBENZENE)-1-ETHANOL;1-(2,4-DIMETHYLPHENYL)ETHAN-1-OL;1-(2,4-DIMETHYLPHENYL)ETHANOL;Nsc78938
• CAS NO: 5379-19-1
• Molecular Formula: C₁₀H₁₄O
• Molecular Weight: 150.22
• Product Categories: Miscellaneous
• Mol File: 5379-19-1.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 225.8°Cat760mmHg
• Flash Point: 100°C
• Appearance: /
• Density: 0.981g/cm³
• Vapor Pressure: 0.048mmHg at 25°C
• Refractive Index: 1.526
• PKA: 14.57±0.20(Predicted)
• CAS DataBase Reference: 1-(2,4-DIMETHYLPHENYL)ETHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,4-DIMETHYLPHENYL)ETHANOL(5379-19-1)
• EPA Substance Registry System: 1-(2,4-DIMETHYLPHENYL)ETHANOL(5379-19-1)

Safety Data

• Hazardous Substances Data: 5379-19-1(Hazardous Substances Data)

Usage

General Description

1-(2,4-dimethylphenyl)ethanol, also known as nebracetam, is an organic chemical compound with the molecular formula C10H14O. This colorless liquid is commonly used in the pharmaceutical industry as an intermediate in the synthesis of various medications, and it is also used in the production of fragrances and flavors. It is a member of the phenethyl alcohol class of compounds and has a slightly floral odor. It is a versatile compound with a wide range of applications, making it a valuable chemical in various industries.

InChI:InChI=1/C10H14O/c1-7-4-5-10(9(3)11)8(2)6-7/h4-6,9,11H,1-3H3

Upstream product

• 102877-07-6 1-(2,4-dimethylphenyl)ethanamine 
• 7446-70-0 aluminium trichloride 
• 107-06-2 1,2-dichloro-ethane 
• 75-36-5 acetyl chloride 
• 108-38-3 m-xylene 
• 64-19-7 acetic acid 
• 89-74-7 2,4-dimethylacetophenone. 
• 64-17-5 ethanol 

Relevant articles and documents

AZAINDOLE COMPOUNDS, SYNTHESIS THEREOF, AND METHODS OF USING THE SAME

The invention provides compounds of formula (I) and methods of treating a Mycobacterium infection or tuberculosis, or inhibiting DprE1 with the same.

NBu4NI-catalyzed direct synthesis of α-ketoamides from aryl methyl ketones with dialkylformamides in water using TBHP as oxidant

A novel and easy practical direct synthesis of α-ketoamides has been developed without metals in water. This procedure was catalyzed by nBu 4NI using TBHP as oxidant from simple substrates, aryl methyl ketones and dialkylformamides. The Royal Society of Chemistry 2012.

Dimethylbenzene derivatives

Compounds of the formula (I): wherein X is a —(C═CH2)— group or a —CH(CH3)— group, with the proviso that when X is a —(C═CH2)— group, R1 is a C1-10 alkyl group or a C2-10 alkenyl group and