| Identification | More | [Name]
3,4,5,6-Tetrachlorophthalonitrile | [CAS]
1953-99-7 | [Synonyms]
3,4,5,6-tetrachlorobenzene-1,2-dicarbonitrile
3,4,5,6-Tetrachlorophthalonitrile
TETRACHLOROPHTHALONITRILE
3,4,5,6-tetrachloro-1,2-benzenedicarbonitrile
3,4,5,6-tetrachloro-2-benzenedicarbonitrile
o-Phthalodinitrile, tetrachloro-
o-Tcpn
o-Tetrachlorophthalodinitrile
Phthalonitrile, tetrachloro-
tetrachloro-o-phthalodinitril
Tetrachlorophthalodinitrile
TETRACHLOROPHTHALONITRILE 98%
3,4,5,6-Thetrachlorophthalonitrile
Z-CHLOROTHALONIL
1,2-Benzenedicarbonitrile, 3,4,5,6-tetrachloro-
2,3,4,5-Tetrachloro-6-(cyanomethyl)phenylacetonitrile
tetrachloro-o-phthalodinitrile | [EINECS(EC#)]
217-783-1 | [Molecular Formula]
C8Cl4N2 | [MDL Number]
MFCD00019740 | [Molecular Weight]
265.91 | [MOL File]
1953-99-7.mol |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H312+H332 | [Precautionary statements ]
P261-P271-P280-P302+P352+P312-P304+P340+P312-P362+P364 | [Hazard Codes ]
Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . | [Safety Statements ]
S36:Wear suitable protective clothing . | [RIDADR ]
UN 3077 9/PG III | [WGK Germany ]
3 | [RTECS ]
TI8225000 | [HS Code ]
2926.90.4801 | [HazardClass ]
9 | [PackingGroup ]
III | [Toxicity]
mouse,LD50,intraperitoneal,66mg/kg (66mg/kg),BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY),Industrial Health. Vol. 4, Pg. 11, 1966. |
| Hazard Information | Back Directory | [Uses]
3,4,5,6-Tetrachlorophthalonitrile can be used as a reagent in chemical reactions or as an intermediate in organic synthesis. 3,4,5,6-Tetrachlorophthalonitrile and 3,4,5,6-Tetrachlorophthalonitrile can be used as substrates with various phenoxy compounds in nucleophilic aromatic substitution reactions to prepare 3,4,6-trihalo-5-p-substituted phenoxyphthalonitrile containing four substituents other than hydrogen[1]. | [Synthesis]
The quantitative o-xylene will be sent to the vaporizer for vaporization, after the o-xylene is vaporized, it will be taken out of the vaporizer by air and mixed with ammonia in the mixer and then enter into the fluidized bed, the molar ratio of three kin | [References]
[1] JIANG-HONG WANG C. L A Khanamiryan. Multisubstituted phthalonitriles for phthalocyanine synthesis[J]. Journal of Porphyrins and Phthalocyanines, 2004. DOI:10.1142/S1088424604000660. |
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