N-Phenylmaleimide

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Names

[ CAS No. ]:
941-69-5

[ Name ]:
N-Phenylmaleimide

[Synonym ]:
N-Phenylmaleimide
N-Phenylmaleimide(N-PMI)
Maleanil
EINECS 213-382-0
phenylmaleimide
1-phenylpyrrole-2,5-dione
MFCD00005502
1-Phenyl-1H-pyrrole-2,5-dione
1-phenyl-2,5-dihydro-1H-pyrrole-2,5-dione
1H-Pyrrole-2,5-dione, 1-phenyl-

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
299.3±9.0 °C at 760 mmHg

[ Melting Point ]:
85-87 °C(lit.)

[ Molecular Formula ]:
C10H7NO2

[ Molecular Weight ]:
173.168

[ Flash Point ]:
136.8±11.1 °C

[ Exact Mass ]:
173.047684

[ PSA ]:
37.38000

[ LogP ]:
1.09

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

[ Index of Refraction ]:
1.630

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
ON5950000
CHEMICAL NAME :
Maleimide, N-phenyl-
CAS REGISTRY NUMBER :
941-69-5
BEILSTEIN REFERENCE NO. :
0125098
LAST UPDATED :
199710
DATA ITEMS CITED :
8
MOLECULAR FORMULA :
C10-H7-N-O2
MOLECULAR WEIGHT :
173.18
WISWESSER LINE NOTATION :
T5VNVJ BR

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
Standard Draize test
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - rabbit
REFERENCE :
SCCUR* Shell Chemical Company. Unpublished Report. (2401 Crow Canyon Rd., San Romon, CA 94583) Volume(issue)/page/year: -,8,1961 ** ACUTE TOXICITY DATA **
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
188 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
SCCUR* Shell Chemical Company. Unpublished Report. (2401 Crow Canyon Rd., San Romon, CA 94583) Volume(issue)/page/year: -,8,1961
TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
25 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: 5,22,1953
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
78 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
SCCUR* Shell Chemical Company. Unpublished Report. (2401 Crow Canyon Rd., San Romon, CA 94583) Volume(issue)/page/year: -,8,1961
TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rabbit
DOSE/DURATION :
100 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
SCCUR* Shell Chemical Company. Unpublished Report. (2401 Crow Canyon Rd., San Romon, CA 94583) Volume(issue)/page/year: -,8,1961 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X9528 No. of Facilities: 10 (estimated) No. of Industries: 1 No. of Occupations: 2 No. of Employees: 30 (estimated) No. of Female Employees: 20 (estimated)

Safety Information

[ Symbol ]:

GHS05, GHS06, GHS09

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H301-H315-H317-H318-H400

[ Precautionary Statements ]:
P273-P280-P301 + P310-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges

[ Hazard Codes ]:
T:Toxic;

[ Risk Phrases ]:
R25;R36/37/38

[ Safety Phrases ]:
S45-S24/25

[ RIDADR ]:
UN 2811 6.1/PG 3

[ WGK Germany ]:
3

[ RTECS ]:
ON5950000

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
2925190090

Synthetic Route

Precursor & DownStream

Precursor

  • Maleic anhydride
  • 2-Butenoic acid,4-oxo-4-(phenylamino)-, (2Z)-
  • Ethyl cis-3-Iodoacrylate (stabilized with Copper chip)
  • Phenylisocyanate
  • 4-Oxo-4-(phenylamino)-2-butenoic acid
  • Maleimide
  • 2-phenyl-1,3,2-dioxaborinane
  • Mequinol

DownStream

  • 4-(CHLOROSULFONYL)BENZOICACID
  • 3-Isochromanone
  • (3aR,4S,9aR)-1,3-dioxo-2-phenyl-2,3,3a,4,9,9a-hexahydro-1H-benzo[f]isoindole-4-carboxylic acid
  • Phosphinic acid,P-methyl-P-phenyl-
  • N-PHENYL-2,3-NAPHTHALIMIDE
  • 3-(4-methoxyphenyl)-1-phenylpyrrole-2,5-dione
  • Fullerene-C60
  • (1R,3aS,6aR)-ethyl 2-methyl-4,6-dioxo-5-phenyloctahydropyrrolo[3,4-c]pyrrole-1-carboxylate
  • 4,7-Epoxy-1H-isoindole-1,3(2H)-dione, 3a,4,7,7a-tetrahydro-2-phenyl-
  • 2-phenyl-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-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

Michael addition/pericyclization/rearrangement--a multicomponent strategy for the synthesis of substituted resorcinols.

Org. Biomol. Chem. 10(31) , 6388-94, (2012)

The combination of methyl 3,7-dioxo-2-diazo-4-octenoate from the zinc triflate catalyzed Mukaiyama-Michael reaction of methyl 3-tert-butylsilyloxy-2-diazobutenoate and 4-methoxy-3-buten-2-one with Mic...

Chemical modification of milk xanthine oxidase with different modifiers.

Prep Biochem Biotechnol. 33(3) , 173-87, (2003)

Xanthine oxidase (XO), purified from buttermilk was subjected to modification with N-phenylmaleimide, p-toluene-sulfonyl chloride, and 2-mercaptobenzimidazole. Spectrophotometric monitoring of the enz...

Behavior of N-phenylmaleimide- and p-phenylenedimaleimide-reacted muscle crossbridge heads.

Biochim. Biophys. Acta 1367(1-3) , 127-33, (1998)

The finding of Barnett et al. (Biophys. J. 61 (1992) 358) that NPM-reacted crossbridge heads do not bind strongly to actin in rigor solution is not easily interpreted in terms of the solution studies ...


More Articles


Related Compounds

  • p-iodo-N-phenylmaleimide
  • 2-bromo-N-phenylmaleimide
  • dimethyl-N-phenylmaleimide
  • 2-Chloro-N-phenylmaleimide
  • 2-Methyl-N-phenylmaleimide
  • 3-anilino-N-phenylmaleimide
  • 1-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanoyl]-4,4-difluoropyrrolidine-2-carboxylic acid
  • 4-[3-(azetidin-1-yl)pyrrolidin-1-yl]-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-oxobutanoic acid
  • 4-{[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclopentyl]formamido}but-2-ynoic acid
  • tert-butyl N-[1-(chlorosulfonyl)-4-methyl-2-(propan-2-yl)pentan-3-yl]carbamate
  • N-[4-(3-fluorophenyl)phenyl]methanesulfonamide
  • 6-(3-Fluoro-2-formylphenyl)pyridazine-3-carboxylic acid
  • 5-({[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-1,2-oxazol-3-yl]formamido}methyl)-1,3-oxazole-4-carboxylic acid
  • (2S)-1-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hex-5-enoyl]-2-methylpyrrolidine-2-carboxylic acid
  • 4-(4-ethynyl-4-hydroxypiperidin-1-yl)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-oxobutanoic acid
  • 4-(7,7-dimethyl-5-oxo-1,4-diazepan-1-yl)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-oxobutanoic acid
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