| Identification | More | [Name]
1-INDANOL | [CAS]
6351-10-6 | [Synonyms]
1H-INDEN-1-OL, 2,3-DIHYDRO-
1-HYDROXYHYDRINDENE
(+/-)-1-HYDROXYINDAN
1-HYDROXYINDAN
1-HYDROXYINDANE
1-INDANAOL
(+/-)-1-INDANOL
1-INDANOL
AURORA KA-6964
INDAN-1-OL
(±)-2,3-dihydro-1H-inden-1-ol
1-Indanole
2,3-Dihydro-1H-inden-1-ol
Indan-1-ol 97%
(±)-1-Hydroxyindan, (±)-1-Indanol
1-Hydroxy-2,3-dihydro-1H-indene | [EINECS(EC#)]
228-755-3 | [Molecular Formula]
C9H10O | [MDL Number]
MFCD00003797 | [Molecular Weight]
134.18 | [MOL File]
6351-10-6.mol |
| Chemical Properties | Back Directory | [Appearance]
white to slightly yellow crystalline solid | [Melting point ]
50-53 °C | [Boiling point ]
128 °C12 mm Hg(lit.) | [density ]
0.8540 (rough estimate) | [refractive index ]
1.5630 (estimate) | [Fp ]
145 °C
| [storage temp. ]
Store at RT. | [solubility ]
Chloroform (Sparingly), Methanol (Slightly) | [form ]
Crystalline Solid | [pka]
14.23±0.20(Predicted) | [color ]
White to slightly yellow | [Water Solubility ]
Soluble in water 10 g/L at 20°C, ethanol, benzene. | [BRN ]
2042960 | [InChIKey]
YIAPLDFPUUJILH-UHFFFAOYSA-N | [CAS DataBase Reference]
6351-10-6(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [RIDADR ]
UN 2811 6.1/PG 3
| [WGK Germany ]
3
| [RTECS ]
NK7300000 | [Hazard Note ]
Irritant | [HazardClass ]
6.1(b) | [PackingGroup ]
III | [HS Code ]
29062990 |
| Hazard Information | Back Directory | [Chemical Properties]
white to slightly yellow crystalline solid | [Uses]
1-Indanol derivative was found to be an efficient ligand for the palladium-catalyzed asymmetric Heck reaction. It is used as pharmaceutical intermediate. | [Definition]
ChEBI: Indan-1-ol is a member of indanes, an aromatic alcohol and a secondary alcohol. It has a role as a xenobiotic. It derives from a hydride of an indane. | [General Description]
Chiral-sensitive aggregation of 1-indanol has been studied by FTIR spectroscopy. Transfer dehydrogenation of 1-indanol has been investigated over heterogeneous palladium catalyst using cyclohexene as hydrogen acceptor. |
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