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110568-64-4

110568-64-4 Structure

110568-64-4 Structure
IdentificationBack Directory
[Name]

6-NITRO-ISOINDOLIN-1-ONE
[CAS]

110568-64-4
[Synonyms]

6-Nitro-1-isoindolinone
6-NITRO-ISOINDOLIN-1-ONE
6-Nitroisoindoline-1-one
6-Nitro-2,3-dihydro-isoindol-1-one
6-nitro-2,3-dihydro-1H-isoindol-1-one
1H-Isoindol-1-one, 2,3-dihydro-6-nitro-
[Molecular Formula]

C8H6N2O3
[MDL Number]

MFCD03093931
[MOL File]

110568-64-4.mol
[Molecular Weight]

178.14
Chemical PropertiesBack Directory
[Melting point ]

253 °C (decomp)
[Boiling point ]

487.5±45.0 °C(Predicted)
[density ]

1.449±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

12.56±0.20(Predicted)
[Appearance]

White to yellow Solid
Questions And AnswerBack Directory
[Uses]

6-Nitroisoindoline-1-one is a heterocyclic derivative that can be used as a pharmaceutical intermediate. It exists in a variety of natural products and pharmaceutical molecules and has extremely high biological activity.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933790090
Spectrum DetailBack Directory
[Spectrum Detail]

6-NITRO-ISOINDOLIN-1-ONE(110568-64-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-BROMOMETHYL-4-NITRO-BENZOIC ACID METHYL ESTER

133446-99-8

6-NITRO-ISOINDOLIN-1-ONE

110568-64-4

General procedure for the synthesis of 6-nitro-isoindolin-1-one from methyl 2-(bromomethyl)-4-nitrobenzoate: Methyl 2-(bromomethyl)-4-nitrobenzoate (250 mg, 0.92 mmol) was added to a methanolic solution of saturated ammonia (5 mL) and stirred for 2 hr at room temperature, and completion of the reaction was monitored by thin layer chromatography (TLC). The solvent was removed by distillation under reduced pressure and ethyl acetate (7 mL) was added to the residue and sonicated for 3 min, followed by placement in a refrigerator at -20 °C for 3 min to promote crystallization. After precipitating a large amount of solid, the product was collected by filtration and dried under high vacuum to give 150 mg of a pale yellow solid in 92% yield.

[References]

[1] Patent: CN103804358, 2016, B. Location in patent: Paragraph 0123
[2] Patent: WO2006/17443, 2006, A2. Location in patent: Page/Page column 155
[3] Patent: WO2012/92880, 2012, A1. Location in patent: Page/Page column 57
[4] Patent: WO2015/81891, 2015, A1. Location in patent: Page/Page column 138; 139
[5] Patent: US9138427, 2015, B2. Location in patent: Page/Page column 287
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