ChemicalBook--->CAS DataBase List--->7223-50-9

7223-50-9

7223-50-9 Structure

7223-50-9 Structure
IdentificationBack Directory
[Name]

N-PROPARGYLPHTHALIMIDE
[CAS]

7223-50-9
[Synonyms]

AKOS BBS-00002599
TIMTEC-BB SBB008979
PropargylphthalaMide
N-PROPARGYLPHTHALIMIDE
N-2-PROPYNYLPHTHALIMIDE
N-prop-2-ynylphthalimide
N-Propargylphthalimide 97%
N-Propargylphthalimide,97%
N-Propargylphthalimide
2-Propargylisoindoline-1,3-dione
2-(2-Propynyl)isoindoline-1,3-dione
2-Propargyl-1H-isoindole-1,3(2H)-dione
2-(Prop-2-yn-1-yl)isoindoline-1,3-dione
2-(2-PROPYNYL)-1H-ISOINDOLE-1,3(2H)-DIONE
[EINECS(EC#)]

230-621-4
[Molecular Formula]

C11H7NO2
[MDL Number]

MFCD00065028
[MOL File]

7223-50-9.mol
[Molecular Weight]

185.18
Chemical PropertiesBack Directory
[Appearance]

Beige to orange powder
[Melting point ]

145-153 °C
[Boiling point ]

304.1±25.0 °C(Predicted)
[density ]

1.318±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

powder to crystal
[pka]

-2.54±0.20(Predicted)
[color ]

White to Light yellow to Light orange
[InChI]

1S/C11H7NO2/c1-2-7-12-10(13)8-5-3-4-6-9(8)11(12)14/h1,3-6H,7H2
[InChIKey]

PAZCLCHJOWLTGA-UHFFFAOYSA-N
[SMILES]

O=C1N(CC#C)C(=O)c2ccccc12
Hazard InformationBack Directory
[Chemical Properties]

Beige to orange powder
[Synthesis]

Potassium phthalimide

1074-82-4

Propargyl bromide

106-96-7

N-PROPARGYLPHTHALIMIDE

7223-50-9

General procedure for the synthesis of N-propargyl phthalimide from phthalimide potassium salt and 3-bromopropargyl: 8.4 mmol of 3-bromopropargyl and 8.4 mmol of phthalimide potassium salt were dissolved in 10 mL of N,N-dimethylformamide. Subsequently, 0.2 g of manganese dioxide solid was added as a catalyst. The reaction mixture was stirred at 28°C for 2 hours. Upon completion of the reaction, the mixture was diluted by adding 100 mL of ethyl acetate to the mixture, followed by washing with water to collect the organic layer. The organic layer was further washed with saturated aqueous sodium chloride solution and dried with anhydrous sodium sulfate. The dried organic phase was separated and purified by column chromatography with the eluent being a solvent mixture of petroleum ether and ethyl acetate (5:1, v/v) to obtain pure N-propargyl phthalimide.

[References]

[1] Patent: CN105669525, 2016, A. Location in patent: Paragraph 0062; 0063; 0082
[2] Molecular Crystals and Liquid Crystals Science and Technology Section A: Molecular Crystals and Liquid Crystals, 2002, vol. 377, p. 13 - 18
[3] Phosphorus, Sulfur and Silicon and the Related Elements, 2004, vol. 179, # 8, p. 1611 - 1614
[4] Patent: WO2005/82892, 2005, A2. Location in patent: Page/Page column 58-59
[5] European Journal of Organic Chemistry, 2017, vol. 2017, # 27, p. 3941 - 3946
Safety DataBack Directory
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

36/37/38-36-22
[Safety Statements ]

37/39-26
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

29251995
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Spectrum DetailBack Directory
[Spectrum Detail]

N-PROPARGYLPHTHALIMIDE(7223-50-9)1HNMR
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