| Identification | More | [Name]
N-Chlorophthalimide | [CAS]
3481-09-2 | [Synonyms]
2-chloro-1h-isoindole-1,3(2h)-dione
N-CHLOROPHTHALIMIDE
ncp
phthalimide chloride
Phthalimidoyl chloride
Chlorophtalimide
N-Chlorphthalimid
2-Chloro-2H-isoindole-1,3-dione | [EINECS(EC#)]
222-459-8 | [Molecular Formula]
C8H4ClNO2 | [MDL Number]
MFCD00023027 | [Molecular Weight]
181.58 | [MOL File]
3481-09-2.mol |
| Chemical Properties | Back Directory | [Appearance]
White to pale yellow powder | [Melting point ]
188-198 °C (lit.) | [Boiling point ]
315.1±25.0 °C(Predicted) | [density ]
1.56±0.1 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,2-8°C | [pka]
-3.53±0.20(Predicted) | [InChIKey]
WDRFYIPWHMGQPN-UHFFFAOYSA-N | [CAS DataBase Reference]
3481-09-2(CAS DataBase Reference) |
| Safety Data | Back 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 . | [RIDADR ]
1759 | [WGK Germany ]
1
| [HazardClass ]
8 | [PackingGroup ]
II | [HS Code ]
29349990 |
| Hazard Information | Back Directory | [Chemical Properties]
White to pale yellow powder | [Uses]
N-Chlorophthalimide may be employed in the synthesis of:
- α-amino acetal
- α-amino nitro compounds
- vicinal diamine
- α,β-unsaturated vicinal haloamino nitro compound
It may also be used as a chlorination reagent for the synthesis of 3-(methylthio)oxindoles. | [General Description]
N-Chlorophthalimide in anhydrous acetic acid serves as a useful oxidizing reagent for use in various direct titrimetric analyses. N-Chlorophthalimide can be synthesized by reacting phthalimide, t-butyl hypochlorite, water and t-butyl alcohol. It participates in the synthesis of 2-amino-3-benzoyl-α-(methylthio)phenylacetamide. |
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