Phthalimide, N-benzyl-

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Names

[ CAS No. ]:
2142-01-0

[ Name ]:
Phthalimide, N-benzyl-

[Synonym ]:
2-Benzylisoindoline-1,3-dione
1H-Isoindole-1,3(2H)-dione, 2-(phenylmethyl)-
2-benzylisoindole-1,3-dione
N-Benzylphthalimide
EINECS 218-395-5
2-benzyl-1H-isoindol-1,3(2H)-dione
2-Benzyl-1,3-isoindolinedione
2-(phenylmethyl)isoindole-1,3-dione
2-(phenylmethyl)-1H-isoindole-1,3(2H)-dione
2-(benzyl)isoindoline-1,3-quinone
MFCD00023077
N-BENZYLPHTALIMIDE
BENZYLPHTHALIMIDE
2-Benzyl-1H-isoindole-1,3(2H)-dione
Phthalimide, N-benzyl-
1H-Isoindole-1,3(2H)-dione,2-(phenylMethyl)

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
393.0±21.0 °C at 760 mmHg

[ Melting Point ]:
114-116 °C(lit.)

[ Molecular Formula ]:
C15H11NO2

[ Molecular Weight ]:
237.253

[ Flash Point ]:
179.8±14.4 °C

[ Exact Mass ]:
237.078979

[ PSA ]:
37.38000

[ LogP ]:
3.33

[ Vapour Pressure ]:
0.0±0.9 mmHg at 25°C

[ Index of Refraction ]:
1.660

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
R20/21/22

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2925190090

Synthetic Route

Precursor & DownStream

Precursor

  • Benzyl alcohol
  • N-methylsulfonylphthalimide
  • Benzylamine
  • Benzyl chloride
  • Methyl 2-iodobenzoate
  • Isocyanatomethylbenzene
  • Methyl 2-bromobenzoate
  • carbon monoxide

DownStream

  • Benzylamine
  • Phthalic acid
  • N-Allylbenzylamine
  • 1,2-Benzenedicarboxamide,N1,N2-bis(phenylmethyl)-
  • N-Methylbenzylamine
  • Dibenzylamine
  • 2-BENZYLISOINDOLINE
  • 2-benzyl-2H-isoindole
  • 2-[(2-nitrophenyl)methyl]isoindole-1,3-dione
  • 2-(4-nitrobenzyl)-1H-isoindole-1,3(2H)-dione

Customs

[ HS Code ]: 2925190090

[ Summary ]:
2925190090 other imides and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Novel and versatile methodology for synthesis of cyclic imides and evaluation of their cytotoxic, DNA binding, apoptotic inducing activities and molecular modeling study.

Eur. J. Med. Chem. 42 , 614-26, (2007)

Versatile method has been developed for synthesis of N-substituted imides. Thus, acid anhydrides, imides and dicarboxylic acids were successfully subjected to dehydrative cyclization with substituted ...

Inhibition of monoamine oxidase by C5-substituted phthalimide analogues.

Bioorg. Med. Chem. 19 , 4829-40, (2011)

Literature reports that isatin as well as C5- and C6-substituted isatin analogues are reversible inhibitors of human monoamine oxidase (MAO) A and B. In general, C5- and C6-substitution of isatin lead...

N-benzylphthalimide. Warzecha K-D, et al.

Acta Crystallogr. Sect. E Struct. Rep. Online 62(6) , 2367-68, (2006)


More Articles


Related Compounds

  • Phthalimide,N,N'-(2-bromotrimethylene)di- (8CI)
  • Phthalimide, N-anilinotetraiodo-
  • 3-(N-benzyl-N-ethylamino)-5-methylphenol
  • 3-((N-benzyl)acetamido)quinuclidine
  • ethyl N-benzyl-N-((ethoxycarbonyl)methyl)succinamate
  • pentacarbonyl(N-benzyl-2-azacyclotridecylidene)chromium(0)
  • 1-[1-(1,2-Oxazol-3-yl)cyclopropyl]methanaminehydrochloride
  • 2-Methoxy-2-(2,3,6-trifluorophenyl)propan-1-amine
  • N-{3-[4-(6-chloro-2-oxo-2,3-dihydro-1H-indol-3-yl)piperidin-1-yl]-3-oxopropyl}prop-2-enamide
  • 3-(2-Fluoro-4-methoxyphenyl)-2-hydroxy-3-methylbutanoic acid
  • 5-{[(4-fluorophenyl)methyl]amino}-2,3-dihydro-1H-1,3-benzodiazol-2-one hydrochloride
  • 2-(1H-indol-5-yl)ethanethioamide
  • 5-(diphenylmethyl)-1-methyl-1H-pyrazol-4-amine
  • 3-[2-(Benzyloxy)phenyl]morpholine
  • methyl 3-(aminomethyl)-5-(1H-1,2,3,4-tetrazol-1-yl)pentanoate
  • N-[4-(3-hydroxyazetidin-3-yl)phenyl]acetamide
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