ChemicalBook--->CAS DataBase List--->15149-10-7

15149-10-7

15149-10-7 Structure

15149-10-7 Structure
IdentificationBack Directory
[Name]

ETHYLENE GLYCOL MONO-P-TOLYL ETHER
[CAS]

15149-10-7
[Synonyms]

YLOTHANE
AI3-09181
p-Cresoxyethanol
Einecs 239-209-9
2-(P-TOLYLOXY)ETHANOL
Ethanol, 2-(p-tolyloxy)-
p-Methylphenyloxyethanol
2-(4-methylphenoxy)-ethano
4-(2-HYDROXYETHOXY)TOLUENE
2-(4-METHYLPHENOXY)ETHANOL
Ethanol,2-(4-methylphenoxy)-
ethyleneglycolmonotolylether
p-Cresol 2-hydroxyethyl ether
Ethanol, 2-(p-tolyloxy)- (8ci)
2-(p-Methylphenoxy)ethylalcohol
ETHYLENE GLYCOL MONO-P-TOLYL ETHER
beta-Hydroxyethyl p-methylphenyl ether
4-(2-Hydroxyethoxy)toluene 2-(4-Methylphenoxy)ethanol
[EINECS(EC#)]

239-209-9
[Molecular Formula]

C9H12O2
[MDL Number]

MFCD00020600
[MOL File]

15149-10-7.mol
[Molecular Weight]

152.19
Chemical PropertiesBack Directory
[Melting point ]

45°C
[Boiling point ]

123°C 8mm
[density ]

1.058±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[pka]

14.30±0.10(Predicted)
[color ]

White to Almost white
[Odor]

at 100.00 %. floral jasmin animal
[Odor Type]

floral
[Cosmetics Ingredients Functions]

PERFUMING
[LogP]

1.686 (est)
[EPA Substance Registry System]

2-(4-Methylphenoxy)ethanol (15149-10-7)
Safety DataBack Directory
[Risk Statements ]

36/37/38-41
[Safety Statements ]

26-36-39
[TSCA ]

TSCA listed
[HS Code ]

2909498090
Spectrum DetailBack Directory
[Spectrum Detail]

ETHYLENE GLYCOL MONO-P-TOLYL ETHER(15149-10-7)MS
ETHYLENE GLYCOL MONO-P-TOLYL ETHER(15149-10-7)1HNMR
ETHYLENE GLYCOL MONO-P-TOLYL ETHER(15149-10-7)13CNMR
ETHYLENE GLYCOL MONO-P-TOLYL ETHER(15149-10-7)IR1
ETHYLENE GLYCOL MONO-P-TOLYL ETHER(15149-10-7)IR2
ETHYLENE GLYCOL MONO-P-TOLYL ETHER(15149-10-7)IR3
ETHYLENE GLYCOL MONO-P-TOLYL ETHER(15149-10-7)Raman
Hazard InformationBack Directory
[Synthesis]

p-Cresol

106-44-5

2-Chloroethanol

107-07-3

ETHYLENE GLYCOL MONO-P-TOLYL ETHER

15149-10-7

The general procedure for synthesizing 2-(4-methylphenoxy)ethanol from p-toluol and 2-chloroethanol was as follows: referring to Example 2 step a; the experimental operation of Example 1a was repeated using 108 g (1 mol) of p-toluol in place of p-(α,α,γ,γ-tetramethylbutyl)phenol, and mixing with 345 g (2.5 mol) of potassium carbonate powder. All other components, dosages and reaction conditions were kept unchanged, and only the addition rate of 2-chloroethanol was adjusted to 1-2 hours. Upon completion of the reaction, 2-(4-methylphenoxy)ethanol was isolated and the product was a yellow to light brown oily residue. The yield of the crude product was 88-92% and the GC purity was 90-95%.

[References]

[1] Patent: EP1892235, 2008, A1. Location in patent: Page/Page column 4
[2] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 6, p. 1557 - 1561
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