O-trimethylsilyl-S-phenylethylene monothioglycol
2-(phenylthio)ethanol
Conditions | Yield |
---|---|
With water; 1,1,1,3,3,3-hexamethyl-disilazane In dichloromethane at 20℃; for 0.616667h; | 96% |
2-(phenylsulfinyl)ethanol
2-(phenylthio)ethanol
Conditions | Yield |
---|---|
With 1,3,5-trichloro-2,4,6-triazine; potassium iodide In acetonitrile at 20℃; for 0.133333h; chemoselective reaction; | 95% |
With titanium(IV) iodide In acetonitrile at 0℃; for 0.166667h; Reduction; | 87% |
With sodium iodide at 20℃; for 4h; Green chemistry; | 87% |
Conditions | Yield |
---|---|
With copper(l) iodide; potassium phosphate tribasic trihydrate at 110℃; for 12h; | 95% |
With potassium phosphate In neat (no solvent) at 70℃; for 9h; | 70% |
With potassium hydroxide In dimethyl sulfoxide at 110℃; for 8h; Inert atmosphere; | 67% |
2-(phenylthio)acetaldehyde
2-(phenylthio)ethanol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at -78℃; | 95% |
2-(phenylthio)ethanol
Conditions | Yield |
---|---|
With triethylamine In dichloromethane for 14h; Irradiation; | 93% |
2-(phenylthio)ethanol
Conditions | Yield |
---|---|
With triethylamine In dichloromethane for 5.5h; Irradiation; | 93% |
Conditions | Yield |
---|---|
With potassium phosphate In neat (no solvent) at 70℃; for 10h; | 40% |
Conditions | Yield |
---|---|
With HKUST-1 metal organic framework In tetrachloromethane at 20℃; Kinetics; | 38% |
Conditions | Yield |
---|---|
With pyrographite | |
With sodium hydroxide |
Conditions | Yield |
---|---|
With sodium ethanolate | |
With sodium hydroxide | |
With sodium hydroxide |
Conditions | Yield |
---|---|
With sodium hydroxide |
oxirane
Tetrathiophosphoric acid diphenyl ester; compound with triethyl-amine
A
2-(phenylthio)ethanol
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In chloroform at -30 - 20℃; for 12h; |
Conditions | Yield |
---|---|
With n-butyllithium; N,N,N,N,-tetramethylethylenediamine Multistep reaction; |
Conditions | Yield |
---|---|
With water Kinetics; Mechanism; |
Conditions | Yield |
---|---|
With potassium hydroxide In N,N-dimethyl acetamide |
A
2-(phenylthio)ethanol
B
N-(2-hydroxyethyl)-naphthalene-2-sulfonamide
Conditions | Yield |
---|---|
With potassium hydroxide In dimethyl sulfoxide at 25℃; Rate constant; var. solvents; |
2-(phenylthio)ethyl brosylate
methylamine
A
2-(phenylthio)ethanol
B
4-bromo-N-(2-hydroxy-ethyl)-benzenesulfonamide
Conditions | Yield |
---|---|
With potassium hydroxide In dimethyl sulfoxide at 25℃; Rate constant; var. solvents; |
2-(phenylthio)ethanol
2-(phenylsulfonyl)ethanol
Conditions | Yield |
---|---|
With dihydrogen peroxide; phosphotungstate-non-cross-linked amphiphilic polymer compl at 50℃; for 4h; | 100% |
With phosphotungstic acid; poly(acrylamide) based ammonium salt; dihydrogen peroxide at 50℃; for 4h; | 100% |
With dihydrogen peroxide; titanium(IV) oxide In acetonitrile at 20℃; for 1.5h; chemoselective reaction; | 100% |
2-(phenylthio)ethanol
2-(phenylsulfinyl)ethanol
Conditions | Yield |
---|---|
With iron(III) chloride; periodic acid In acetonitrile at 0 - 25℃; for 0.416667h; | 100% |
With aluminum(III) nitrate nonahydrate; sulfuric acid; silica gel; silica gel; sodium bromide In dichloromethane; water at 20℃; for 3.5h; chemoselective reaction; | 99% |
With water; ammonium bromide In dichloromethane at 20℃; for 8h; chemoselective reaction; | 99% |
2-(phenylthio)ethanol
2-(phenylthio)acetaldehyde
Conditions | Yield |
---|---|
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In ethyl acetate for 8h; Heating; | 100% |
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In dimethyl sulfoxide at 20℃; for 4h; | 90% |
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In dimethyl sulfoxide at 10 - 30℃; for 8h; | 42% |
2-(phenylthio)ethanol
tert-butyldimethylsilane
1-(t-BuMe2Si)-2-(t-BuMe2Si-S)ethyl ether
Conditions | Yield |
---|---|
With palladium dichloride In N,N-dimethyl acetamide at 24.85℃; for 3h; | 100% |
Conditions | Yield |
---|---|
With carbon tetrabromide; Cu(tmp)(BINAP)BF4; sodium bromide In N,N-dimethyl-formamide for 24h; Appel Halogenation; UV-irradiation; Inert atmosphere; | 99% |
With sulfurous dibromide; N,N-dimethyl-formamide In cyclohexane at 20℃; for 3h; Bromination; | 98% |
With phosphorus tribromide at 20℃; for 0.5h; | 98% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 9h; | 99% |
Conditions | Yield |
---|---|
With 1,3,5-trichloro-2,4,6-triazine; N,N-dimethyl-formamide In dichloromethane at 25℃; for 48h; | 98% |
With thionyl chloride | 96% |
With hydrogenchloride; tetrafluoroboric acid In hydrogenchloride | 72.4% |
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran at 0℃; for 0.0833333h; | 98% |
2-(phenylthio)ethanol
C26H19NO3
C28H23NO3S
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran at 0℃; for 0.0833333h; | 96% |
With 18-crown-6 ether; caesium carbonate In acetonitrile at 25℃; for 12h; |
2-(phenylthio)ethanol
A
2-(phenylsulfinyl)ethanol
B
2-(phenylsulfonyl)ethanol
Conditions | Yield |
---|---|
With dihydrogen peroxide In water at 30℃; for 1h; | A 94% B 6% |
With dihydrogen peroxide at 50℃; for 4h; | A 80% B 13% |
With (Bu4N)2[{MoO(O2)2}2(μ-O)]; dihydrogen peroxide In acetonitrile for 2h; Time; | A 66% B 30% |
(2-hydroxyethyl)(methyl)amine
bis(trichloromethyl) carbonate
2-(phenylthio)ethanol
Conditions | Yield |
---|---|
Stage #1: bis(trichloromethyl) carbonate; 2-(phenylthio)ethanol With pyridine In tetrahydrofuran at 20℃; for 0.75h; Cooling with ice; Stage #2: With pyridine; 1-hydroxy-pyrrolidine-2,5-dione In tetrahydrofuran at 20℃; for 0.5h; Stage #3: (2-hydroxyethyl)(methyl)amine In tetrahydrofuran at 20℃; for 2h; Cooling with ice; | 93% |
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran at 25℃; for 0.166667h; | 92% |
2-(phenylthio)ethanol
D-glucal triacetate
Acetic acid (2R,3S)-2-acetoxymethyl-6-(2-phenylsulfanyl-ethoxy)-3,6-dihydro-2H-pyran-3-yl ester
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In benzene for 0.133333h; Ambient temperature; | 92% |
Conditions | Yield |
---|---|
With ruthenium(III) acetate at 20℃; for 24h; | 92% |
Conditions | Yield |
---|---|
With 18-crown-6 ether; caesium carbonate In acetonitrile at 25℃; for 45h; | 91% |
2-(phenylthio)ethanol
trifluoroacetic anhydride
2-(phenylthio)ethyl trifluoroacetate
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 0℃; for 2h; | 91% |
2-amino-benzthiazole
2-(phenylthio)ethanol
N-(2-(phenylthio)ethyl)benzo[d]thiazol-2-amine
Conditions | Yield |
---|---|
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; sodium hydroxide at 150℃; for 12h; Inert atmosphere; regioselective reaction; | 91% |
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran at 0℃; for 0.0833333h; | 90% |
With 18-crown-6 ether; caesium carbonate In acetonitrile at 25℃; for 12h; |
2-(phenylthio)ethanol
5'-O-tert-butyldimethylsilyl-3'-O-(4,4'-dimethoxytriphenylmethyl)thymidine
1-[4-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-5-methyl-3-(2-phenylsulfanyl-ethyl)-1H-pyrimidine-2,4-dione
Conditions | Yield |
---|---|
With tributylphosphine; 1,1'-azodicarbonyl-dipiperidine In benzene at 20℃; for 18h; Mitsunobu reaction; | 90% |
1-(4-nitrophenyl)-5-tetrazolone
2-(phenylthio)ethanol
diethylazodicarboxylate
Conditions | Yield |
---|---|
With triphenylphosphine In tetrahydrofuran | 90% |
1-(4-nitrophenyl)-5-tetrazolone
2-(phenylthio)ethanol
Conditions | Yield |
---|---|
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran for 12h; | 90% |
2-(phenylthio)ethanol
methacrylic acid methyl ester
2-phenylthioethyl methacrylate
Conditions | Yield |
---|---|
With titanium(IV) isopropylate; 2,4-dimethyl-6-tert-butylphenol; pyrographite In cyclohexane at 90 - 92℃; | 90% |
2-(phenylthio)ethanol
1,1,1,3,3,3-hexamethyl-disilazane
O-trimethylsilyl-S-phenylethylene monothioglycol
Conditions | Yield |
---|---|
With asymmetric salen type di-Schiff base-based zinc complex supported on Fe3O4 nanoparticles at 20℃; for 0.416667h; | 89% |
With cross-linked poly((30percent)4-vinylpyridine/(70percent)styrene) copolymer-supported bismuth(III) triflate In dichloromethane at 20℃; for 0.166667h; | 86% |
With chloro-trimethyl-silane |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene for 3h; Heating; | 89% |
IUPAC Name: 2-Phenylsulfanylethanol
Synonyms of Ethanol,2-(phenylthio)- (CAS NO.699-12-7): 2-Phenylmercaptoethanol ; AI3-17423 ; EINECS 211-828-9 ; NSC 57851 ; Phenylthioethanol ; 2-(Phenylthio)ethanol
CAS NO: 699-12-7
Molecular Formula of Ethanol,2-(phenylthio)- (CAS NO.699-12-7): C8H10OS
Molecular Weight: 154.2294
Molecular Structure:
ProductCategories: Alkohols
Polar Surface Area: 34.53 Å2
Index of Refraction: 1.592
Molar Refractivity: 45.55 cm3
Molar Volume: 134.5 cm3
Surface Tension: 47.5 dyne/cm
Density of Ethanol,2-(phenylthio)- (CAS NO.699-12-7): 1.14 g/cm3
Flash Point: 131.5 °C
Enthalpy of Vaporization: 54.61 kJ/mol
Boiling Point: 278.4 °C at 760 mmHg
Vapour Pressure: 0.00205 mmHg at 25°C
Hazard Codes: Xi
Risk Statements: 36
R36: Irritating to eyes.
Safety Statements: 23-24/25
S23: Do not breathe vapour.
S24/25: Avoid contact with skin and eyes.
WGK Germany: 3
TSCA: T
HazardClass: STENCH
HS Code: 29309070
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