3-phenyl-2-propanol
1-phenyl-2-chloropropane
Conditions | Yield |
---|---|
With oxalyl dichloride; 1-methyl-3-(2-(3-methyl-2-oxoimidazolidin-1-yl)ethyl)-1H-imidazol-3-ium hexafluorophosphate at 20 - 60℃; | 95% |
With tetrachlorosilane In tetrachloromethane at 25℃; for 0.5h; | 80% |
With gallium(III) trichloride; dimethylmonochlorosilane; diethyl (2R,3R)-tartrate In dichloromethane; pentane at 20℃; for 1h; Inert atmosphere; | 69% |
3-phenyl-2-propanol
3,3-dichloro-1,2-diphenylcyclopropene
A
1-phenyl-2-chloropropane
B
diphenylcyclopropenone
Conditions | Yield |
---|---|
In acetonitrile at 80℃; for 0.333333h; Inert atmosphere; | A 95% B n/a |
1-phenyl-2-propyl 2-(methoxyethoxyethylcarboxy)-1-benzosulfonate
1-phenyl-2-chloropropane
Conditions | Yield |
---|---|
With lithium chloride In acetone for 8h; | 94% |
With lithium chloride In acetone for 8h; Product distribution / selectivity; Heating / reflux; | 94% |
(±)-1-phenylpropanyl-2-yl methansulfonate
1-phenyl-2-chloropropane
Conditions | Yield |
---|---|
With 1-butyl-3-methylimidazolium chloride at 60℃; for 8h; Inert atmosphere; Green chemistry; | 94% |
1-phenyl-2-chloropropane
Conditions | Yield |
---|---|
With indium(III) chloride; benzil In dichloromethane at 20℃; for 7h; | 82% |
1-phenyl-2-propyl benzenesulphonate
1-phenyl-2-chloropropane
Conditions | Yield |
---|---|
With benzyltri(n-butyl)ammonium chloride In acetone for 0.5h; Reflux; | 82% |
With lithium chloride; manganese(ll) chloride In tetrahydrofuran Inert atmosphere; Reflux; | 60% |
Conditions | Yield |
---|---|
With lithium chloride; copper dichloride; lithium tetrachloropalladate(II) |
iron(III) chloride
allyl alcohol
benzene
1-phenyl-2-chloropropane
Conditions | Yield |
---|---|
at 80℃; |
iron(III) chloride
allyl alcohol
benzene
A
allylbenzene
B
1-phenyl-2-chloropropane
Conditions | Yield |
---|---|
at 25℃; |
iron(III) chloride
3-chloroprop-1-ene
benzene
A
1-phenyl-2-chloropropane
B
1,2-diphenylpropane
Conditions | Yield |
---|---|
at -10℃; | |
at -20 - -10℃; |
3-chloroprop-1-ene
benzene
A
1-phenylpropene
B
1-phenyl-2-chloropropane
aluminium trichloride
nitromethane
3-chloroprop-1-ene
benzene
A
1-phenyl-2-chloropropane
B
1,2-diphenylpropane
Conditions | Yield |
---|---|
at 5℃; |
1-phenyl-2-chloropropane
Conditions | Yield |
---|---|
With diethyl ether Einleiten von HCl; |
Propylbenzene
A
1-phenyl-2-chloropropane
B
phenylpropyl chloride
C
(1-Chloro-propyl)-benzene
Conditions | Yield |
---|---|
With chlorine In tetrachloromethane for 0.0833333h; Photolysis; |
1-phenyl-2-chloropropane
Conditions | Yield |
---|---|
With sulfuryl dichloride; sodium chloride at 60℃; Kinetics; Activation energy; Further Variations:; Temperatures; |
3-chloroprop-1-ene
benzene
A
allylbenzene
B
1-phenyl-2-chloropropane
Conditions | Yield |
---|---|
With oxygen at 110℃; |
Conditions | Yield |
---|---|
Stage #1: 1-phenyl-2-chloropropane; pentan-3-one With 4,4'-di-tert-butylbiphenyl; lithium In tetrahydrofuran at 25℃; for 1h; Schlenk technique; Inert atmosphere; Stage #2: With water In tetrahydrofuran at 0 - 25℃; Schlenk technique; Cooling with ice; | 74% |
2,3-dimethyl-2,3-butane diol
1-phenyl-2-chloropropane
2-(1-phenylpropan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Conditions | Yield |
---|---|
Stage #1: 1-phenyl-2-chloropropane; 1,3-dimethyl-2-(tributylstannyl)-2,3-dihydro-1H-benzo[d][1,3,2]diazaborole With 1,1'-azobis(1-cyanocyclohexanenitrile) In n-heptane at 100℃; for 6h; Inert atmosphere; Glovebox; Sealed tube; Stage #2: 2,3-dimethyl-2,3-butane diol With hydrogenchloride In 1,4-dioxane; n-heptane; water at 20℃; for 2h; Inert atmosphere; Glovebox; Sealed tube; | 60% |
dimethylmonochlorosilane
1-phenyl-2-chloropropane
Conditions | Yield |
---|---|
With iodine; magnesium In tetrahydrofuran for 17h; Inert atmosphere; Reflux; | 47% |
1-phenyl-2-chloropropane
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane
2-(1-phenylpropan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Conditions | Yield |
---|---|
Stage #1: 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane With bis(cyclopentadienyl)titanium dichloride; lithium methanolate In tert-butyl methyl ether for 0.5h; Stage #2: 1-phenyl-2-chloropropane In tert-butyl methyl ether at 100℃; under 760.051 Torr; for 24h; Inert atmosphere; | 41% |
Stage #1: 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane With bis(cyclopentadienyl)titanium dichloride; lithium methanolate In tert-butyl methyl ether for 0.5h; Inert atmosphere; Glovebox; Stage #2: 1-phenyl-2-chloropropane In tert-butyl methyl ether at 100℃; for 24h; Sealed tube; | 41% |
C-(1-methyl-4-phenyl-piperidin-4-yl)-methylamine
1-phenyl-2-chloropropane
(1-methyl-2-phenyl-ethyl)-(1-methyl-4-phenyl-[4]piperidylmethyl)-amine
Conditions | Yield |
---|---|
at 110℃; |
1-phenyl-2-chloropropane
2-amino-1-phenylpropane
Conditions | Yield |
---|---|
With ethanol; ammonia at 160℃; |
Conditions | Yield |
---|---|
With ethanol at 160℃; |
carbon dioxide
1-phenyl-2-chloropropane
2-methyl-3-phenylpropanoic acid
Conditions | Yield |
---|---|
With magnesium In diethyl ether |
1-phenyl-2-chloropropane
orthoformic acid triethyl ester
2-benzylpropionaldehyde
Conditions | Yield |
---|---|
(i) Mg, Et2O, (ii) aq. HCl; Multistep reaction; |
carbon monoxide
1-phenyl-2-chloropropane
benzene
(±)-2-methyl-2-phenyl-2,3-dihydro-1H-inden-1-one
Conditions | Yield |
---|---|
With aluminium trichloride at 23 - 25℃; |
methanol
1-phenyl-2-chloropropane
A
allylbenzene
B
1-propenylbenzene
C
(1-methoxypropyl)benzene
D
methyl 1-phenyl-2-propyl ether
E
benzaldehyde
Conditions | Yield |
---|---|
With Methyl fluoride; oxygen at 37.5℃; Product distribution; Irradiation; 0.6 Torr substrate, 700 Torr bulk gas, 4 Torr O2 and 1.9 Torr methanol partial pressures; |
methanol
1-phenyl-2-chloropropane
A
allylbenzene
B
cis-1-phenyl-1-propylene
C
(1-methoxypropyl)benzene
D
methyl 1-phenyl-2-propyl ether
E
benzaldehyde
Conditions | Yield |
---|---|
With C3H8 bulk gas; oxygen at 37.5℃; Product distribution; Irradiation; 0.5 Torr substrate, 700 Torr bulk gas, 4 Torr O2 and 2.0 Torr methanol partial pressures; |
methanol
1-phenyl-2-chloropropane
A
1-propenylbenzene
B
cis-1-phenyl-1-propylene
C
(1-methoxypropyl)benzene
D
methyl 1-phenyl-2-propyl ether
E
benzaldehyde
Conditions | Yield |
---|---|
With oxygen; deuterium at 37.5℃; Product distribution; Irradiation; 0.5 Torr substrate, 750 Torr bulk gas, 4 Torr O2 and 2.5 Torr methanol partial pressures; | |
With methane; oxygen at 37.5℃; Product distribution; Irradiation; different partial pressures of components and in the given case: in the presence of 4 Torr NMe3 partial pressure; |
para-xylene
1-phenyl-2-chloropropane
A
1-phenyl-11-(2,5-dimethylphenyl)propane
Conditions | Yield |
---|---|
With iron(III) chloride In carbon disulfide at 40℃; for 0.2h; Yield given. Yields of byproduct given; | |
With iron(III) chloride In carbon disulfide at 0℃; for 3h; Yield given. Yields of byproduct given; |
1-phenyl-2-chloropropane
Spiro(piperidine-4,6'-dibenz-1,4-oxathiepin)
C26H27NOS*ClH
Conditions | Yield |
---|---|
With sodium hydroxide In dimethyl sulfoxide at 120℃; for 3.5h; | 0.2 g |
The Benzene,(2-chloropropyl)- is an organic compound with the formula C9H11Cl. The IUPAC name of this chemical is 2-chloropropylbenzene. With the CAS registry number 10304-81-1, it is also named as 1-Phenyl-2-chloropropane.
Physical properties about Benzene,(2-chloropropyl)- are: (1)ACD/LogP: 3.22; (2)#Freely Rotating Bonds: 2; (3)Index of Refraction: 1.513; (4)Molar Refractivity: 45.24 cm3; (5)Molar Volume: 150.5 cm3; (6)Polarizability: 17.93×10-24cm3; (7)Surface Tension: 32.5 dyne/cm; (8)Density: 1.027 g/cm3; (9)Flash Point: 79.7 °C; (10)Enthalpy of Vaporization: 42.91 kJ/mol; (11)Boiling Point: 211.1 °C at 760 mmHg; (12)Vapour Pressure: 0.27 mmHg at 25°C.
You can still convert the following datas into molecular structure:
(1)SMILES: ClC(Cc1ccccc1)C
(2)InChI: InChI=1/C9H11Cl/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8H,7H2,1H3
(3)InChIKey: CKWAHIDVXZGPES-UHFFFAOYAH
(4)Std. InChI: InChI=1S/C9H11Cl/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8H,7H2,1H3
(5)Std. InChIKey: CKWAHIDVXZGPES-UHFFFAOYSA-N
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