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ChemicalBook--->CAS DataBase List--->5332-26-3

5332-26-3

5332-26-3 Structure

5332-26-3 Structure
IdentificationMore
[Name]

N-(Bromomethyl)phthalimide
[CAS]

5332-26-3
[Synonyms]

N-(BROMOMETHYL)PHTALIMIDE
N-(BROMOMETHYL)PHTHALIMIDE
N-PHTHALIMIDOMETHYL BROMIDE
PHTHALIMIDOMETHYL BROMIDE
1H-Isoindole-1,3(2H)-dione, 2-(bromomethyl)-
2-(Bromomethyl)-1H-isoindole-1,3(2H)-dione
2-(bromomethyl)-1h-isoindole-3(2h)-dione
Phthalimide, N-(bromomethyl)-
N-(Bromomethyl)phthalimide,98+%
2-(Bromomethyl)isoindole-1,3-dione
2-(Bromomethyl)isoindoline-1,3-dione
[EINECS(EC#)]

226-239-2
[Molecular Formula]

C9H6BrNO2
[MDL Number]

MFCD00005897
[Molecular Weight]

240.05
[MOL File]

5332-26-3.mol
Chemical PropertiesBack Directory
[Appearance]

white powder
[Melting point ]

152-155 °C(lit.)
[Boiling point ]

318.9±25.0 °C(Predicted)
[density ]

1.6838 (rough estimate)
[refractive index ]

1.6120 (estimate)
[storage temp. ]

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
[form ]

Crystalline Powder
[pka]

-2.72±0.20(Predicted)
[color ]

White to off-white
[Water Solubility ]

decomposes
[Sensitive ]

Moisture & Light Sensitive
[BRN ]

140943
[InChIKey]

UUSLLECLCKTJQF-UHFFFAOYSA-N
[CAS DataBase Reference]

5332-26-3(CAS DataBase Reference)
[NIST Chemistry Reference]

N-bromomethylphthalimide(5332-26-3)
[EPA Substance Registry System]

5332-26-3(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 .
S37/39:Wear suitable gloves and eye/face protection .
[WGK Germany ]

3
[F ]

8-10-21
[TSCA ]

Yes
[HS Code ]

29251995
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

N-(Bromomethyl)phthalimide(5332-26-3).msds
Hazard InformationBack Directory
[Chemical Properties]

white powder
[Uses]

N-(Bromomethyl)phthalimide was used as initiator in synthesis of α-phthalimidopoly(styrene) by atom transfer radical polymerisation. It was also used in synthesis of functionalized 5-(aminomethyl)pyrimidine-2,4,6-trione analog and new bis-C(cage)-substituted o-carborane.
Spectrum DetailBack Directory
[Spectrum Detail]

N-(Bromomethyl)phthalimide(5332-26-3)MS
N-(Bromomethyl)phthalimide(5332-26-3)1HNMR
N-(Bromomethyl)phthalimide(5332-26-3)13CNMR
N-(Bromomethyl)phthalimide(5332-26-3)IR1
N-(Bromomethyl)phthalimide(5332-26-3)IR2
N-(Bromomethyl)phthalimide(5332-26-3)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

N-(Bromomethyl)phthalimide, 97%(5332-26-3)
[Alfa Aesar]

N-(Bromomethyl)phthalimide, 95%(5332-26-3)
[Sigma Aldrich]

5332-26-3(sigmaaldrich)
[TCI AMERICA]

N-(Bromomethyl)phthalimide,>96.0%(T)(5332-26-3)
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