Phthalimide, N-benzyl-
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
DownStream
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
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)