- Isoindoline
- Isoindoline hydrochloride
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Cas Database |
| Name |
Isoindoline |
EINECS | N/A |
| CAS No. | 496-12-8 | Density | 1.04 g/cm3 |
| PSA | 12.03000 | LogP | 1.61860 |
| Solubility | N/A | Melting Point |
17 °C(lit.) |
| Formula | C8H9N | Boiling Point | 199.6 °C at 760 mmHg |
| Molecular Weight | 119.166 | Flash Point | 75.8 °C |
| Transport Information | N/A | Appearance | COLORLESS TO ORANGE TO BROWN LIQUID |
| Safety | 26-36 | Risk Codes | 36/37/38 |
| Molecular Structure |
|
Hazard Symbols |
 Xi
|
| Synonyms |
Isoindoline(6CI,7CI,8CI);1,3-Dihydro-2H-isoindole;1,3-Dihydroisoindole;2,3-Dihydro-1H-isoindole; |
Article Data | 65 |
Isoindoline Synthetic route
- 32372-83-1
2(toluene-p-sulphonyl)isoindoline
- 496-12-8
isoindoline
| Conditions | Yield |
|---|---|
| With hydrogen bromide; propionic acid; phenol for 2h; Inert atmosphere; Reflux; | 93% |
| With hydrogen bromide; phenol In propionic acid for 2h; Heating; | 61% |
| With hydrogen bromide; propionic acid; phenol |
- 53175-33-0
N-(2-furylmethyl)-N-(prop-2-en-1-yl)amine
- 496-12-8
isoindoline
| Conditions | Yield |
|---|---|
| With hydrogenchloride; sodium hydrogencarbonate 1.) ether, 90 deg C, 32 h, 2.) H2O; | 85% |
- 35180-14-4
2-benzylisoindoline
- 496-12-8
isoindoline
| Conditions | Yield |
|---|---|
| With palladium on activated charcoal; hydrogen In methanol | 84% |
| With iodine; hypophosphorous acid; acetic acid for 12h; Heating; | 75% |
| With ethanol; palladium | |
| With hydrogen; palladium on activated charcoal In methanol at 20℃; for 8h; | |
| With palladium 10% on activated carbon; hydrogen In methanol at 20℃; for 8h; |
| Conditions | Yield |
|---|---|
| With sodium cyanoborohydride In methanol at 25℃; for 3h; | 80% |
- 136918-14-4
phthalimide
- 496-12-8
isoindoline
| Conditions | Yield |
|---|---|
| With borane-THF In tetrahydrofuran for 14h; Inert atmosphere; Reflux; | 78% |
| With borane-THF In tetrahydrofuran for 14h; Heating; | 50% |
| With sulfuric acid at 60℃; bei der elektrolytischen Reduktion; |
| Conditions | Yield |
|---|---|
| platinum In tetrahydrofuran | 75% |
| With cobalt catalyst; ammonia at 100℃; under 73550.8 Torr; Hydrogenation.Reagens 4: Dioxan; | |
| With ammonia; nickel at 100℃; under 73550.8 Torr; Hydrogenation.Reagens 4: Dioxan; |
| Conditions | Yield |
|---|---|
| With ammonia; potassium carbonate In water at 120℃; for 0.333333h; microwave irradiation; | 62% |
| With hydrogenchloride; hexamethylenetetramine; triethylamine 1.) CHCl3, reflux, 4 h; 2.) EtOH, 12 h; 3.) reflux, 8 h; | 44% |
| Conditions | Yield |
|---|---|
| With sulfuric acid at 50℃; Electrolysis.Verwendung einer Cadmium-Kathode; | |
| With dimethylsulfide borane complex In tetrahydrofuran at 0 - 45℃; for 3h; Inert atmosphere; |
| Conditions | Yield |
|---|---|
| With sulfuric acid at 40℃; Bei der elektrochemischen Reduktion an einer Zink-Amalgam-Kathode unter Normaldruck,bei 5.3 at und bei 8.5 at; |
| Conditions | Yield |
|---|---|
| bei der elektrochemischen Reduktion an einer Blei-Kathode in wss. H2SO4; |
Isoindoline Chemical Properties
IUPAC Name: 2,3-dihydro-1H-isoindole
Synonyms of 1H-Isoindole,2,3-dihydro- (CAS NO.496-12-8): dihydroisoindole ; isoindoline ; 2,3-dihydro-1h-isoindole ; 1,3-Dihydroisoindole ; 1,3-Dihydro-2H-isoindole ; o-Xyleneimine
CAS NO: 496-12-8
Molecular Formula of 1H-Isoindole,2,3-dihydro- (CAS NO.496-12-8): C8H9N
Molecular Weight: 119.1638
Molecular Structure:
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H bond acceptors: 1
H bond donors: 1
Polar Surface Area: 3.24 Å2
Index of Refraction: 1.562
Molar Refractivity: 37.16 cm3
Molar Volume: 114.5 cm3
Surface Tension: 38.9 dyne/cm
Density of 1H-Isoindole,2,3-dihydro- (CAS NO.496-12-8): 1.04 g/cm3
Flash Point: 75.8 °C
Enthalpy of Vaporization: 43.58 kJ/mol
Boiling Point: 199.6 °C at 760 mmHg
Vapour Pressure: 0.338 mmHg at 25°C
Isoindoline Safety Profile
Hazard Codes: 
Xi
Risk Statements: 36/37/38
R36/37/38: Irritating to eyes, respiratory system and skin.
Safety Statements: 26-36
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36: Wear suitable protective clothing.
WGK Germany: 3
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