5-Hydroxy-1-indanone

Names

[ Name ]:
5-Hydroxy-1-indanone

[Synonym ]:
5-Hydroxy-2,3-dihydro-1H-inden-1-on
5-hydroxy-2,3-dihydro-1H-inden-1-one
1H-Inden-1-one, 2,3-dihydro-4-hydroxy-
4-Hydroxy-1-indanone
5-Hydroxy-1-indanone
MFCD00857527
5-hydroxy-2,3-dihydro-1H-indene-1-one
5-hydroxy-indan-1-one
4-hydroxyindan-1-one
5-hydroxy-1-oxo-2,3-dihydro-1H-indene
5-hydroxyindan-1-one
5-Hydroxyindanone
4-hydroxy-2,3-dihydro-1H-inden-1-one
1-oxo-5-indanol
1H-Inden-1-one, 2,3-dihydro-5-hydroxy-
4-Hydroxy-2,3-dihydro-1H-inden-1-on

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
343.8±31.0 °C at 760 mmHg

[ Melting Point ]:
175 °C (dec.)(lit.)

[ Molecular Formula ]:
C₉H₈O₂

[ Molecular Weight ]:
148.159

[ Flash Point ]:
146.4±17.4 °C

[ Exact Mass ]:
148.052429

[ PSA ]:
37.30000

[ LogP ]:
1.86

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.631

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2914400090

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2914400090

[ Summary ]:
2914400090 other ketone-alcohols and ketone-aldehydes。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

Articles

Synthesis and inhibition study of monoamine oxidase, indoleamine 2,3-dioxygenase and tryptophan 2,3-dioxygenase by 3,8-substituted 5H-indeno[1,2-c]pyridazin-5-one derivatives.

Eur. J. Med. Chem. 46(12) , 6104-11, (2011)

Previous studies on 5H-indeno[1,2-c]pyridazin-5-one derivatives as inhibitors of MAO-B revealed that it was possible to increase the MAO-B inhibitory potency of 5H-indeno[1,2-c]pyridazin-5-ones by sub...

On the involvement of single-bond rotation in the primary photochemistry of photoactive yellow protein. Stahl AD, et al.

Biophys. J. 101(5) , 1184-1192, (2011)

Geometric and solvent effects on intramolecular phenolic hydrogen abstraction by carbonyl n,p* and p,p* triplets. Lathioor EC and Leigh WJ.

Can. J. Chem. 79(12) , 1851-1863, (2001)

Related Compounds

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