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5-Fluoroisatin

Names

[ CAS No. ]:
443-69-6

[ Name ]:
5-Fluoroisatin

[Synonym ]:
5-Fluoroisatin
5-Fluoro-2,3-indolinedione
5-fluoroindoline-2,3-dione
1H-Indole-2,3-dione, 5-fluoro-
5-Fluoroindole-2,3-dione
5-Fluoro-1H-indole-2,3-dione
5-Fluoro-2,3-indoledione
MFCD00022795

Biological Activity

[Description]:

5-Fluoroisatin is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
417.9ºC at 760mmHg

[ Melting Point ]:
224-227 °C(lit.)

[ Molecular Formula ]:
C8H4FNO2

[ Molecular Weight ]:
165.12

[ Flash Point ]:
206.5ºC

[ Exact Mass ]:
165.022614

[ PSA ]:
46.17000

[ LogP ]:
0.61

[ Index of Refraction ]:
1.584

[ Storage condition ]:
Refrigerator

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-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933990090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Counter-Current chromatography separation of isatin derivatives using the sandmeyer methodology. Almeida MR, et al.

J. Braz. Chem. Soc. 21(4) , 764-9, (2010)

A Novel Preparation of a-Substituted Tryptamines from Isatins. Franklin CS and White AC.

J. Chem. Soc. 2 , 1335-37, (1963)

¹⁹F magnetic resonance probes for live-cell detection of peroxynitrite using an oxidative decarbonylation reaction.

Chem. Commun. (Camb.) 50(82) , 12311-4, (2014)

We report a newly discovered oxidative decarbonylation reaction of isatins that is selectively mediated by peroxynitrite (ONOO(-)) to provide anthranilic acid derivatives. We have harnessed this rapid...


More Articles


Related Compounds