ChemicalBook--->CAS DataBase List--->550-44-7

550-44-7

550-44-7 Structure

550-44-7 Structure
IdentificationMore
[Name]

N-Methylphthalimide
[CAS]

550-44-7
[Synonyms]

2-METHYL-1H-ISOINDOLE-1,3(2H)-DIONE
METHYL PHTHALIMIDE
N-METHYLPHTHALIMIDE
PHTHALIMIDE-N-METHYL
1H-Isoindole-1,3(2H)-dione,2-methyl-
2-Methyl-1H-isoindol-1,3(2H)-dion
2-methyl-1h-isoindole-3(2h)-dione
2-Methyl-isoindole-1,3-dione
n-methyl-phthalimid
N-Methylphthalimide,98%
n-methyl-1h-isoindole-1,3-(2h)-dione
2-Methylisoindoline-1,3-dione
[EINECS(EC#)]

208-982-4
[Molecular Formula]

C9H7NO2
[MDL Number]

MFCD00023063
[Molecular Weight]

161.16
[MOL File]

550-44-7.mol
Chemical PropertiesBack Directory
[Melting point ]

129-132 °C (lit.)
[Boiling point ]

286.05°C
[density ]

1.2443 (rough estimate)
[refractive index ]

1.4500 (estimate)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

-2.09±0.20(Predicted)
[color ]

White to Off-White
[BRN ]

124428
[CAS DataBase Reference]

550-44-7(CAS DataBase Reference)
[NIST Chemistry Reference]

1H-Isoindole-1,3(2H)-dione, 2-methyl-(550-44-7)
[EPA Substance Registry System]

550-44-7(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

1
[RTECS ]

TI5602700
[TSCA ]

Yes
[HazardClass ]

IRRITANT
[HS Code ]

29251900
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

N-Methylphthalimide(550-44-7).msds
Hazard InformationBack Directory
[Chemical Properties]

White powder
[Uses]

Photoreduction of N-methylphthalimide (NMP) with 2,3-dimethyl-2-butene h and the selective electroreduction of N-methylphthalimide to 3-hydroxy-2-methyl-isoindolin-1-one have been studied.
[Synthesis Reference(s)]

The Journal of Organic Chemistry, 44, p. 497, 1979 DOI: 10.1021/jo01318a005
[General Description]

Photoreduction of N-methylphthalimide (NMP) with 2,3-dimethyl-2-butene has been studied. The selective electroreduction of N-methylphthalimide to 3-hydroxy-2-methyl-isoindolin-1-one in ionic liquids and phenol as a proton donor under silent and ultrasonic conditions has been reported. Single electron transfer (SET)-induced photochemical reaction of NMP with silyl enol ether has been investigated. Nitration of NMP is reported to afford “exclusively” 3-nitro-derivative.
[Purification Methods]

Recrystallise the imide from absolute EtOH or AcOH (m 134o). The IR has max at 1780 and 1380cm -1. [Beilstein 21 H 461, 21 III/IV 5030.]
Spectrum DetailBack Directory
[Spectrum Detail]

N-Methylphthalimide(550-44-7)MS
N-Methylphthalimide(550-44-7)1HNMR
N-Methylphthalimide(550-44-7)13CNMR
N-Methylphthalimide(550-44-7)IR1
N-Methylphthalimide(550-44-7)IR2
N-Methylphthalimide(550-44-7)Raman
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

N-Methylphthalimide, 98%(550-44-7)
[Sigma Aldrich]

550-44-7(sigmaaldrich)
[TCI AMERICA]

N-Methylphthalimide,>99.0%(GC)(N)(550-44-7)
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