Conditions | Yield |
---|---|
With trichloroacetamide; triphenylphosphine In dichloromethane at 30℃; for 0.25h; | 99% |
Stage #1: 2-phenylethanol With N,N-dimethylthiourea In dichloromethane at 20℃; Stage #2: With N-chloro-succinimide In dichloromethane at 20℃; for 1h; Irradiation; | 98% |
With 1,3,5-trichloro-2,4,6-triazine; N,N-dimethyl-formamide In dichloromethane at 25℃; for 0.25h; | 97% |
Conditions | Yield |
---|---|
With thionyl chloride In dichloromethane for 1h; Heating; | A 99% B 97% |
2-phenylethyl mesylate
2-phenylethyl chloride
Conditions | Yield |
---|---|
With 1-butyl-3-methylimidazolium chloride at 50℃; for 1h; Inert atmosphere; Green chemistry; | 98% |
diphenethyl-1,1 trimethylene-4,4' bipiperidine
2-phenylethyl chloride
Conditions | Yield |
---|---|
With phenyl chloroformate In neat (no solvent) Heating; | 93% |
2-phenylethanol
3,3-dichloro-1,2-diphenylcyclopropene
A
2-phenylethyl chloride
B
diphenylcyclopropenone
Conditions | Yield |
---|---|
In dichloromethane at 23℃; for 0.25h; Mechanism; Solvent; Inert atmosphere; | A 89% B n/a |
In dichloromethane at 23℃; for 0.25h; |
2-phenylethanol
Benzotrichlorid
A
benzylidene dichloride
B
2-phenylethyl chloride
Conditions | Yield |
---|---|
With TOP; phenylsilane In neat (no solvent) at 100℃; for 24h; Appel Halogenation; Inert atmosphere; | A n/a B 88% |
1-chloro-4-(2-chloroethyl)benzene
2-phenylethyl chloride
Conditions | Yield |
---|---|
With palladium on activated charcoal; formic acid; N,N-dimethyl-formamide for 5h; Heating; | 85% |
Conditions | Yield |
---|---|
With dichloromethylsilane; iron(III) chloride In 1,2-dimethoxyethane for 4h; Heating; | 85% |
Conditions | Yield |
---|---|
With titanium tetrachloride In 1,2-dichloro-ethane for 3h; Reflux; | 85% |
2-phenylethanol
benzoyl chloride
A
2-Phenylethyl benzoate
B
2-phenylethyl chloride
Conditions | Yield |
---|---|
With 2,3-diethyl-2-cyclopropen-1-one In tert-butyl methyl ether at 40℃; for 15h; | A n/a B 83% |
1-methoxy-2-phenylethane
A
2-phenylethyl chloride
B
acetic acid phenethyl ester
Conditions | Yield |
---|---|
With acetyl chloride; zinc In Petroleum ether at 28℃; for 4h; | A 78% B 20% |
1-methoxy-2-phenylethane
acetyl chloride
A
2-phenylethyl chloride
B
acetic acid phenethyl ester
Conditions | Yield |
---|---|
With zinc In Petroleum ether at 28℃; for 4h; | A 78% B 20% |
Conditions | Yield |
---|---|
With potassium hydrogencarbonate; phenyl chloroformate Heating; | 74% |
With methanol; carbonochloridic acid 1-chloro-ethyl ester 1) 1,2-dichloroethane; Yield given. Multistep reaction; |
ethylbenzene
A
1-(1,2-dichloroethyl)benzene
B
2-phenylethyl chloride
C
(1-chloroethyl)benzene
Conditions | Yield |
---|---|
With N-chloro-succinimide; benzophenone In acetonitrile at 27℃; for 24h; Catalytic behavior; Reagent/catalyst; Solvent; Wavelength; Irradiation; regioselective reaction; | A 19 %Spectr. B 7 %Spectr. C 72% |
Conditions | Yield |
---|---|
With N-chloro-succinimide; N-hydroxyphthalimide; 2,3-dicyano-5,6-dichloro-p-benzoquinone In acetonitrile at 80℃; for 16h; Time; Sealed tube; Inert atmosphere; | A 22% B 71% |
With N-chloro-succinimide; acetophenone In acetonitrile at 27℃; for 24h; Irradiation; regioselective reaction; | A 13 %Spectr. B 70% |
With chlorine bei Tageslicht; |
n-butyllithium
(-)-(RS,R)-1-chloro-2-phenylethyl p-tolyl sulfoxide
5,5-dimethyl-2-(2-phenylethyl)benzo-1,3,2-dioxaborinate
B
butyl(p-tolyl)sulfoxide
C
2-phenylethyl chloride
Conditions | Yield |
---|---|
Stage #1: n-butyllithium; (-)-(RS,R)-1-chloro-2-phenylethyl p-tolyl sulfoxide; 5,5-dimethyl-2-(2-phenylethyl)benzo-1,3,2-dioxaborinate In tetrahydrofuran; hexane at -78 - 0℃; for 2.5h; Stage #2: With sodium hydroxide; dihydrogen peroxide In tetrahydrofuran; hexane; water at 20℃; for 2.5h; | A n/a B 53% C 10% D 70% |
Conditions | Yield |
---|---|
With phenyl chloroformate In neat (no solvent) Heating; | 62% |
2-phenylethanol
p-toluenesulfonyl chloride
A
2-phenylethyl tosylate
B
2-phenylethyl chloride
Conditions | Yield |
---|---|
Stage #1: 2-phenylethanol; p-toluenesulfonyl chloride With dmap; triethylamine In dichloromethane at 0 - 5℃; Stage #2: In methanol; dichloromethane at 40 - 42℃; for 7h; | A 58% B 32% |
1-p-Toluolsulfonyl-1-phenethyl-hydrazin
A
2-phenylethyl chloride
B
p-toluenesulfonyl chloride
Conditions | Yield |
---|---|
With N-chloro-succinimide In tetrahydrofuran for 16h; Ambient temperature; Irradiation; | A 57% B n/a |
2-phenylethanol
dimethyl sulfoxide
A
bis(2-phenylethyloxy)methane
B
2-phenylethyl chloride
Conditions | Yield |
---|---|
With 2,4-Dichloro-6-methoxy-1,3,5-triazine In toluene at 80℃; for 4h; | A 50% B 32% |
styrene
2-phenylethyl chloride
Conditions | Yield |
---|---|
With 4-Methoxybenzenethiol; 10-methyl-9-(2,4,6-trimethylphenyl) acridinium tetrafluoroborate; 2,6-lutidine hydrochloride In chloroform; 2,2,2-trifluoroethanol for 24h; Irradiation; Inert atmosphere; | 49% |
2-phenylethanol
hexanoic acid
A
2-phenylethyl ester of hexanoic acid
B
formic acid phenethyl ester
C
2-phenylethyl chloride
Conditions | Yield |
---|---|
With pyridine; N,N-dimethylchloromethyleniminium chloride Ambient temperature; | A 26% B 29% C 39% |
With pyridine; N,N-dimethylchloromethyleniminium chloride Ambient temperature; | A 26% B 39% C 39% |
2-phenethyl iodide
n-octylmagnesium chloride
A
styrene
B
Hexadecane
C
1,4-diphenylbutane
D
decylbenzene
E
2-phenylethyl chloride
Conditions | Yield |
---|---|
With C32H30ClN2NiP In tetrahydrofuran; N,N-dimethyl acetamide at -20℃; for 0.5h; Kumada coupling reaction; Inert atmosphere; | A 20 %Chromat. B 13 %Chromat. C 16% D 29 %Chromat. E 23 %Chromat. |
4,4,5,5-tetramethyl-2-phenethyl-1,3,2-dioxaborolane
(-)-(RS,R)-1-chloro-2-phenylethyl p-tolyl sulfoxide
A
(S)-2-(1,4-diphenyl-2-butyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
B
(Z)-1,4-diphenylbut-2-ene
C
(E)-1,4-diphenylbut-2-ene
D
2-phenylethyl chloride
Conditions | Yield |
---|---|
With tert.-butyl lithium In toluene; pentane at -78 - 20℃; for 15h; Title compound not separated from byproducts.; | A n/a B n/a C n/a D 13% |
Conditions | Yield |
---|---|
at 43℃; |
Conditions | Yield |
---|---|
reagiert analog mit weiteren Aryl-magneisumhalogeniden; |
Conditions | Yield |
---|---|
With phosphorus pentachloride |
Conditions | Yield |
---|---|
durch Chlorierung im diffusen Tageslicht; | |
With chlorine |
Conditions | Yield |
---|---|
With diethyl ether |
2-phenethyl iodide
2-phenylethyl chloride
Conditions | Yield |
---|---|
With Iodine monochloride |
propionyl chloride
2-phenylethyl chloride
4-(2-chloroethyl)propiophenone
Conditions | Yield |
---|---|
With aluminium trichloride In 1,2-dichloro-ethane for 0.416667h; Ambient temperature; | 100% |
aluminium trichloride In 1,2-dichloro-ethane | |
aluminium trichloride In 1,2-dichloro-ethane |
Conditions | Yield |
---|---|
18-crown-6 ether In tert-butyl alcohol at 40℃; Rate constant; Mechanism; secondary α-deuterium isotope effects investigated; also in absence of catalyst; | 100% |
2-phenylethyl chloride
methyl 5-hydroxy-2-nitro-benzoate
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 18h; | 100% |
2-phenylethyl chloride
bis(2-phenylethyl)sulfide
Conditions | Yield |
---|---|
Stage #1: 2-phenylethyl chloride With thiourea Stage #2: With sodium hydroxide Stage #3: 2-phenylethyl chloride | 98% |
With potassium sulfide; ethanol | |
With sodium sulfide; ethanol | |
With sodium sulfide In dimethyl sulfoxide |
2-phenylethyl chloride
2-hydroxy-2-methylpropanenitrile
dihydrocinnamonitrile
Conditions | Yield |
---|---|
Stage #1: 2-hydroxy-2-methylpropanenitrile With lithium hydroxide monohydrate In tetrahydrofuran at 50℃; for 1h; Stage #2: 2-phenylethyl chloride In tetrahydrofuran | 97.9% |
Conditions | Yield |
---|---|
With iron(III) sulfate; water In toluene at 110℃; for 1h; Ionic liquid; | 97% |
With sodium carbonate at 160 - 165℃; | |
With sodium carbonate at 175℃; |
4-n-chlorophenylacetylene
2-phenylethyl chloride
1-chloro-4-(4-phenylbut-1-yn-1-yl)benzene
Conditions | Yield |
---|---|
With copper(l) iodide; C21H23ClNiP2S; caesium carbonate; sodium iodide In dimethyl sulfoxide at 50℃; for 12h; Sonogashira Cross-Coupling; Schlenk technique; Inert atmosphere; | 97% |
2-phenylethyl chloride
1-chloro-2-pentachlorophenylethane
Conditions | Yield |
---|---|
With disulfur dichloride; aluminium trichloride; sulfuryl dichloride at 80℃; for 3h; | 96% |
With disulfur dichloride; aluminium trichloride; sulfuryl dichloride at 70 - 85℃; |
Product Name: 1-Chloro-2-phenylethane
CAS Registry Number: 622-24-2
IUPAC Name: 1-chloro-2-ethylbenzene
Molecular Weight: 140.61006 [g/mol]
Molecular Formula: C8H9Cl
XLogP3: 3.5
Surface Tension: 33.8 dyne/cm
EINECS: 210-725-6
Density: 1.052 g/cm3
Flash Point: 66.7 °C
Melting Point: -60 °C
Refractive index: n20/D 1.53(lit.)
Water Solubility: 0.1 g/L (20 ºC)
Enthalpy of Vaporization: 41.67 kJ/mol
Boiling Point: 198.2 °C at 760 mmHg
Vapour Pressure: 0.512 mmHg at 25°C
Product Categories: Benzene derivates
Following is the molecular structure of 1-Chloro-2-phenylethane (CAS NO.622-24-2) is:
Safty information about 1-Chloro-2-phenylethane (CAS NO.622-24-2) is:
Hazard Codes:
Xi
Risk Statements:
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements:
S23:Do not breathe vapour.
S24/25:Avoid contact with skin and eyes.
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.
WGK Germany: 3
HS Code: 29036990
1-Chloro-2-phenylethane (CAS NO.622-24-2) is a clear, colorless liquid.
First Aid Measures about it:
Eyes: Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid.
Skin: Get medical aid. Flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes.
Ingestion: Get medical aid. Wash mouth out with water.
Inhalation: Remove from exposure and move to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get medical aid.
Handling and Storage about it:
Handling: Avoid breathing dust, vapor, mist, or gas. Avoid contact with skin and eyes.
Storage: Keep away from sources of ignition. Store in a cool, dry place. Store in a tightly closed container.
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