T56 BVNVJ C1

Suppliers

Names

[ CAS No. ]:
550-44-7

[ Name ]:
T56 BVNVJ C1

[Synonym ]:
EINECS 208-982-4
1H-Isoindole-1,3(2H)-dione, 2-methyl-
PHTHALIMIDE-N-METHYL
T56 BVNVJ C1
2-Methylisoindoline-1,3-dione
METHYL PHTHALIMIDE
2-methyl-2,3-dihydro-1H-isoindole-1,3-dione
2-Methyl-1H-isoindole-1
2-methyl-isoindole-1,3-dione
N-Methylphthalimide
2-Methyl-1H-isoindole-1,3(2H)-dione
MFCD00023063
n-methyl-phthalimid
N-methyl phthalimide

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
286.0±0.0 °C at 760 mmHg

[ Melting Point ]:
129-132 °C(lit.)

[ Molecular Formula ]:
C9H7NO2

[ Molecular Weight ]:
161.157

[ Flash Point ]:
117.4±11.1 °C

[ Exact Mass ]:
161.047684

[ PSA ]:
37.38000

[ LogP ]:
1.56

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.607

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
TI5602700
CHEMICAL NAME :
Phthalimide, N-methyl-
CAS REGISTRY NUMBER :
550-44-7
BEILSTEIN REFERENCE NO. :
0124428
LAST UPDATED :
199710
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C9-H7-N-O2

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD - Lethal dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
>500 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
NCNSA6 National Academy of Sciences, National Research Council, Chemical-Biological Coordination Center, Review. (Washington, DC) Volume(issue)/page/year: 5,23,1953

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
1

[ RTECS ]:
TI5602700

[ HS Code ]:
2925190090

Synthetic Route

Precursor & DownStream

Precursor

  • 2-Iodobenzoic acid
  • carbon monoxide
  • methylamine
  • Methanol
  • 2-(4-(METHYLSULFINYL)BUTYL)ISOINDOLINE-1,3-DIONE
  • methyl iodide
  • Potassium phthalimide
  • Benzenecarboximidic acid, N-methyl- (9CI)
  • Phthalic anhydride

DownStream

  • methylamine
  • Phthalic acid
  • 2-methyl-5-nitro-isoindole-1,3-dione
  • 1H-Isoindole-1,3(2H)-dione,2-methyl-4-nitro-
  • 1-methyl-5-thioxopyrrolidin-2-one
  • 1-methyldithiosuccinimide
  • 1,2-Benzenedicarboxamide, N,N'-dimethyl-
  • 2-(ethoxymethyl)isoindole-1,3-dione
  • 3-Acetylindole
  • 1-(1H-Indol-6-yl)ethanone

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

Electroreduction of N-methylphthalimide in room temperature ionic liquids under insonated and silent conditions.

Ultrason. Sonochem. 12(6) , 423-8, (2005)

The selective electroreduction N-methylphthalimide to 3-hydroxy-2-methyl-isoindolin-1-one has been performed in ionic liquids using phenol as a proton donor under silent and ultrasonic conditions. A s...

Photoreduction of N-methylphthalimide with 2, 3-dimethyl-2-butene. Evidence for reaction through an electron transfer generated ion pair. Mazzocchi PH and Klingler L.

J. Am. Chem. Soc. 106(24) , 7567-72, (1984)

Single electron transfer induced photoaddition reactions of silyl enol ether to N-methylphthalimide. Oh SW, et al.

Bull. Korean Chem. Soc. 28(4) , 629, (2007)


More Articles


Related Compounds

  • T56 BVNVJ C1U1
  • T56 BVNVJ C1- BL3TJ AVN2&2 AR
  • T56 BVNVJ C1YQ1MR D- AT6NV DOTJ &&R Form
  • T56 BVNVJ C1- DT5NVOTJ AR D-AT6NV DOTJ &&S Form
  • Amlodipine intermediate
  • 3-Phthalimidopropionaldehyde
  • 5-[1-(2-Pyridinyl)-1h-pyrazolo[3,4-b]pyridin-4-yl]-4-pyrimidinamine
  • (6-(3-Methoxypropoxy)naphthalen-2-yl)boronic acid
  • Benzyl (2-(4-amino-3-(p-tolyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-2-methylpropyl)carbamate
  • 2-(4-Chloro-3-(difluoromethoxy)phenyl)acetic acid
  • Bis-retinamido methylpentane
  • 1-(6-Methoxy-3-trifluoromethyl-pyridin-2-yl)-ethanone
  • Tert-butyl (5-bromonaphthalen-2-YL)carbamate
  • 1-({imidazo[1,2-a]pyridin-2-yl}methyl)-1H-pyrazole
  • 4-Chloro-N-[(3R)-1-(phenylmethyl)-3-pyrrolidinyl]butanamide
  • 2-chloro-1H-1,8-naphthyridin-4-one
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