Conditions | Yield |
---|---|
With L-Selectride In tetrahydrofuran at 67℃; for 72h; | 92% |
With 1-methyl-pyrrolidin-2-one; potassium carbonate; 2-amino-benzenethiol for 0.25h; Heating; | 90% |
(4-ethoxyphenyl)boronic acid
4-Ethoxyphenol
Conditions | Yield |
---|---|
With dihydrogen peroxide In water at 20℃; | 88% |
With tert-butylammonium hexafluorophosphate(V); N,N'-dimethyl-4,4'-bipyridinium dihexafluorophosphate; triethylamine In N,N-dimethyl-formamide Electrochemical reaction; | 68% |
4-ethoxyphenyl benzyl ether
4-Ethoxyphenol
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol at 20℃; under 760 Torr; Hydrogenolysis; | 87% |
With palladium 10% on activated carbon; ammonium formate In tetrahydrofuran; ethanol |
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 70h; Heating; | A 11% B 83% |
Conditions | Yield |
---|---|
With phosphomolybdic acid for 6h; Heating; | 78% |
Conditions | Yield |
---|---|
In hexane; dichloromethane -78 deg C, 1 h, then room temp., 2 h; | 77% |
In diethyl ether |
Conditions | Yield |
---|---|
With Amberlyst-15 for 4h; Reflux; | 69% |
hydroquinone
Diethyl carbonate
A
4-Ethoxyphenol
B
1,4-diethoxybenzene
Conditions | Yield |
---|---|
With Magnesium-Aluminum layered double oxides catalyst at 149.84℃; under 760.051 Torr; for 12h; Autoclave; Inert atmosphere; Irradiation; Green chemistry; | A 60.5% B 15.7% |
Conditions | Yield |
---|---|
With triethylaluminum In toluene at -78℃; for 2h; | A 8 % Spectr. B 56% |
ethylaluminum dichloride
p-benzoquinone
A
4-Ethoxyphenol
B
hydroquinone
Conditions | Yield |
---|---|
In toluene at -78℃; for 2h; | A 26 % Spectr. B 50% |
Conditions | Yield |
---|---|
With copper(I) oxide; sodium methylate In methanol at 185℃; for 12h; Autoclave; | 45% |
Conditions | Yield |
---|---|
Stage #1: hydroquinone With pyridine; poly(ethylene glycol) 4000; oxalyl dichloride In dichloromethane at 20℃; for 18h; Stage #2: C2H5-halide With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 18h; Stage #3: With sodium hydroxide at 20℃; for 2h; | 33.7% |
Conditions | Yield |
---|---|
With copper(I) oxide; sodium methylate In methanol at 185℃; for 12h; Autoclave; | A 30% B 25% |
Conditions | Yield |
---|---|
beim Belichten.Irradiation; |
4-diazo-2,5-cyclohexadienone
4-Ethoxyphenol
Conditions | Yield |
---|---|
With ethanol Einwirkung von Licht; |
Diethyl-(4-ethoxy-phenyl)-phosphat
4-Ethoxyphenol
Conditions | Yield |
---|---|
With potassium hydroxide |
trichloro-acetic acid-(4-ethoxy-phenyl ester)
4-Ethoxyphenol
Conditions | Yield |
---|---|
With sodium hydroxide; nitrobenzene at 40℃; | |
With potassium hydroxide |
Conditions | Yield |
---|---|
durch Aethylierung; |
sodium 4-hydroxybenzen-1-olate
ethyl ester of p-toluenesulfonic acid
A
4-Ethoxyphenol
B
1,4-diethoxybenzene
Conditions | Yield |
---|---|
With methanol |
Conditions | Yield |
---|---|
With oxygen at 120 - 140℃; |
Conditions | Yield |
---|---|
With 2,3,5-trimethyl-pyridine; copper(l) iodide Heating; |
Conditions | Yield |
---|---|
(i) Li, (ii) B2H6, (iii) aq. NaOH, H2O2; Multistep reaction; |
4-ethoxy-2,4,6-tri-tertbutylcyclohexa-2,5-dienone
4-Ethoxyphenol
Conditions | Yield |
---|---|
With aluminium trichloride; toluene In nitromethane |
4-Ethoxyphenol
Conditions | Yield |
---|---|
With sulfuric acid |
hydrogenchloride
A
4-Ethoxyphenol
B
1-chloro-4-ethoxybenzene
C
2-ethoxy-1-nitronaphthalene
D
1-{4-ethoxy-benzeneazo}-2-naphthol
4-Ethoxyphenol
4-Ethoxyphenol
4-ethoxycyclohexan-1-ol
Conditions | Yield |
---|---|
With nickel(II) oxide; hydrogen; palladium In hexane at 80℃; under 22502.3 Torr; for 10h; | 99% |
With hydrogen In water at 20℃; under 7500.75 Torr; for 8h; Autoclave; | 94.8% |
With ethanol; nickel at 200℃; under 102971 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
With pyridine r.t., 2 h, 70 deg C, 2 h; | 98% |
Conditions | Yield |
---|---|
With Oxone; 4-iodophenoxyacetic acid In 2,2,2-trifluoroethanol; water at 20℃; for 0.5h; | 97% |
With bis-[(trifluoroacetoxy)iodo]benzene In water; acetonitrile for 0.166667h; Ambient temperature; | 93% |
With oxone; tetrabutylammomium bromide In water; acetonitrile at 20℃; for 1h; | 92% |
With Oxone In water; acetonitrile at 20℃; for 17h; | 79% |
bis(trichloromethyl) carbonate
4-Ethoxyphenol
4-(ethoxy)phenyl chloroformate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0℃; for 12h; | 97% |
Conditions | Yield |
---|---|
In water at 50℃; | 97% |
Conditions | Yield |
---|---|
With 4-pyrrolidin-1-ylpyridine; triethylamine In dichloromethane for 3h; Heating; | 95% |
With triethylamine In butanone at 0 - 20℃; for 3h; |
4-Ethoxyphenol
β-D-glucose pentaacetate
Acetic acid (2R,3R,4S,5R,6S)-3,5-diacetoxy-2-acetoxymethyl-6-(4-ethoxy-phenoxy)-tetrahydro-pyran-4-yl ester
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In benzene for 8h; Ambient temperature; | 95% |
4-Ethoxyphenol
Conditions | Yield |
---|---|
With phosphate buffer; dihydrogen peroxide; horseradish peroxidase In isopropyl alcohol at 20℃; for 3h; pH=7; | 94% |
1-(tert-butyl) 4-ethyl 4-[(4-fluorophenyl)sulfonyl]piperidine-1,4-dicarboxylate
4-Ethoxyphenol
C27H35NO8S
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 24h; | 94% |
4-Ethoxyphenol
Conditions | Yield |
---|---|
With phosphate buffer; dihydrogen peroxide; horseradish peroxidase In propan-1-ol at 20℃; for 3h; pH=7; | 93% |
4-Ethoxyphenol
Conditions | Yield |
---|---|
Stage #1: 4-Ethoxyphenol With caesium carbonate In acetonitrile for 2h; Stage #2: N-(3-bromophenethyl)-2-chloroacetamide In acetonitrile for 15h; | 92% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone; toluene for 8h; Heating; | 91% |
4-Ethoxyphenol
N,N-dimethyl-formamide dimethyl acetal
1-ethoxy-4-methoxybenzene
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 140℃; for 1h; Microwave irradiation; | 91% |
Conditions | Yield |
---|---|
With potassium carbonate In tert-butyl alcohol at 20℃; for 12h; | 91% |
Conditions | Yield |
---|---|
Stage #1: formaldehyd; 4-Ethoxyphenol With sodium t-butanolate In water at 20℃; for 48h; Stage #2: With hydrogenchloride In dichloromethane; water pH=3; | 91% |
Conditions | Yield |
---|---|
With potassium carbonate; bis-[(trifluoroacetoxy)iodo]benzene In acetonitrile for 0.166667h; Ambient temperature; | 90% |
With Ni0.64Al0.36(OH)2[(WO4)0.045(NO3)027]*0.6H2O; dihydrogen peroxide; ammonium bromide In water; ethyl acetate at 60℃; | 92 % Chromat. |
With [bis(acetoxy)iodo]benzene at 0 - 20℃; Inert atmosphere; |
4-Ethoxyphenol
4,4'-(decane-1,1'-diylbis(oxy))dibenzoic acid
C40H46O8
Conditions | Yield |
---|---|
With pyridine r.t., 2 h, 70 deg C, 2 h; | 90% |
Conditions | Yield |
---|---|
at 20℃; for 0.583333h; Sonication; Neat (no solvent); | 90% |
Conditions | Yield |
---|---|
With 2,3-dicyano-5,6-dichloro-p-benzoquinone | 90% |
With 2,3-dicyano-5,6-dichloro-p-benzoquinone at 20℃; for 0.25h; | 90% |
Conditions | Yield |
---|---|
With pyridine r.t., 2 h, 70 deg C, 2 h; | 88% |
Conditions | Yield |
---|---|
With tetrabutylammomium bromide; potassium carbonate In acetone Reflux; Inert atmosphere; | 88% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 12h; Reflux; | 88% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 48h; Reflux; Inert atmosphere; | 87% |
With potassium carbonate In acetone Reflux; | 83% |
With potassium carbonate In acetone for 16h; Reflux; | 83% |
4-Ethoxyphenol
Conditions | Yield |
---|---|
With triethylamine In benzene N2; exclusion of light; 70-75°C; 4-9 h;; filtered at room temp.; evapd.; dissolved in CH2Cl2; chromd. (SiO2, benzene/CH2Cl2); recrystd. from benzene; elem. anal.;; | 87% |
With triethylamine In toluene N2; exclusion of light; 70-75°C; 4-9 h;; filtered at room temp.; evapd.; dissolved in CH2Cl2; chromd. (SiO2, benzene/CH2Cl2); recrystd. from benzene; elem. anal.;; | 87% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 48h; Reflux; Inert atmosphere; | 87% |
4-Ethoxyphenol
Conditions | Yield |
---|---|
Stage #1: 4-Ethoxyphenol With caesium carbonate In acetonitrile for 2h; Stage #2: 2-chloro-N-(3-(cyclopentyloxy)phenethyl)acetamide In acetonitrile for 15h; | 86% |
4-Ethoxyphenol
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl acetamide at 160℃; for 2h; Inert atmosphere; | 86% |
Product Name: 4-Ethoxyphenol (CAS NO.622-62-8)
Molecular Formula: C8H10O2
Molecular Weight: 138.16g/mol
Mol File: 622-62-8.mol
EINECS: 210-748-1
Melting Point: 64-67 °C
Boiling point: 246.4 °C at 760 mmHg
Flash Point: 124 °C
Density: 1.076 g/cm3
Water Solubility: sightly soluble
Index of Refraction: 1.526
Molar Refractivity: 39.44 cm3
Molar Volume: 128.3 cm3
Surface Tension: 38 dyne/cm
Enthalpy of Vaporization: 50.31 kJ/mol
Vapour Pressure: 0.0173 mmHg at 25°C
XLogP3-AA: 1.8
H-Bond Donor: 1
H-Bond Acceptor: 2
Structure Descriptors of 4-Ethoxyphenol (CAS NO.622-62-8):
IUPAC Name: 4-ethoxyphenol
Canonical SMILES: CCOC1=CC=C(C=C1)O
InChI: InChI=1S/C8H10O2/c1-2-10-8-5-3-7(9)4-6-8/h3-6,9H,2H2,1H3
InChIKey: LKVFCSWBKOVHAH-UHFFFAOYSA-N
Product Categories: Liquid Crystal intermediates; Aromatic Phenols; Anthraquinones, Hydroquinones and Quinones; Phenetole; Building Blocks for Liquid Crystals; Functional Materials; Phenols (Building Blocks for Liquid Crystals)
Intermediates of Liquid Crystals
1. | ipr-mus LDLo:250 mg/kg | RBPMAZ Revue Belge de Pathologie et de Medecine Experimentale. 22 (1952),1. |
Reported in EPA TSCA Inventory.
Poison by intraperitoneal route. Experimental reproductive effects. An irritant. When heated to decomposition it emits acrid smoke and irritating fumes.
Hazard Codes Xn,Xi
Risk Statements 41-37/38-22-36/37/38
R41:Risk of serious damage to the eyes.
R37/38:Irritating to respiratory system and skin.
R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements 37/39-26-36
S37/39:Wear suitable gloves and eye/face protection.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36:Wear suitable protective clothing.
RTECS SL3790000
4-Ethoxyphenol , its CAS NO. is 622-62-8, the synonyms are Ether monoethylique de l'hydroquinone ; Hydroquinone monoethyl ether ; Phenol, 4-ethoxy- ; Phenol, p-ethoxy- ; p-Ethoxyphenol ; p-Hydroxyphenetole .
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