ChemicalBook--->CAS DataBase List--->25369-33-9

25369-33-9

25369-33-9 Structure

25369-33-9 Structure
IdentificationBack Directory
[Name]

7-Chlorooxindole
[CAS]

25369-33-9
[Synonyms]

7-Chloro-2-Oxindole
7-Chloro-2-oxyindole
7-Chloro-2-oxindole98%
7-Chloro-2-oxindole 97%
7-Chloro-2-oxoindole >98%
7023 7-CHLOROINDOLIN-2-ONE
Indol-2-one, 5-chloro-1,3-dihydro-
7-Chloro-2-oxindole in stock Factory
2H-Indol-2-one, 7-chloro-1,3-dihydro-
7-Chloro-2-oxindole/7-chloro-1,3-dihydro-2H-indol-2-one
7-Chloro-1,3-dihydro-2H-indol-2-one, 7-Chloroindolin-2-one
[EINECS(EC#)]

625-279-1
[Molecular Formula]

C8H6ClNO
[MDL Number]

MFCD06656001
[MOL File]

25369-33-9.mol
[Molecular Weight]

167.59
Chemical PropertiesBack Directory
[Melting point ]

221-225 °C
[Boiling point ]

341.0±42.0 °C(Predicted)
[density ]

1.362±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[pka]

13.08±0.20(Predicted)
[InChI]

1S/C8H6ClNO/c9-6-3-1-2-5-4-7(11)10-8(5)6/h1-3H,4H2,(H,10,11)
[InChIKey]

FPDLUAACCNVSQA-UHFFFAOYSA-N
[SMILES]

Clc1cccc2CC(=O)Nc12
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-52/53
[Safety Statements ]

61
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

2933790090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Aquatic Chronic 3
Hazard InformationBack Directory
[Synthesis]

7-CHLOROISATIN

7477-63-6

7-chloroindolin-2-one

25369-33-9

General procedure for the synthesis of 7-chloroindolin-2-one from 7-chloroindigo: Indigo derivatives (1a-j, 3.0 g), 80% hydrazine hydrate (13 mL) and water (13 mL) were added to a three-necked flask equipped with a thermometer under vigorous stirring. The reaction mixture was placed in an oil bath at 140 °C for 6 h and subsequently cooled to room temperature. The pH of the reaction mixture was adjusted to 2 with 2.0 mol/L hydrochloric acid and stirring was continued for 12 hours at room temperature. Upon completion of the reaction, the products were collected by vacuum filtration and recrystallized with anhydrous ethanol to finally obtain the target compounds 2a-j.

[References]

[1] Journal of Chemical Research, 2017, vol. 41, # 9, p. 537 - 540
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