1,3-Dinitro-2-chloro-5-trifluoromethylbenzene RC06315

4-Chloro-3,5-dinitrobenzotrifluoride

Benzene,2-chloro-1,3-dinitro-5-(trifluoromethyl)-;Toluene,4-chloro-α,α,α-trifluoro-3,5-dinitro-;2-Chloro-1,3-dinitro-5-(trifluoromethyl)benzene;4-Chloro-3,5-dinitrobenzotrifluoride;2,6-Dinitro-4-(trifluoromethyl)chlorobenzene;3,5-Dinitro-4-chlorobenzotrifluoride;4-Chloro-3,5-dinitro-α,α,α-trifluorotoluene;4-(Trifluoromethyl)-2,6-dinitrochlorobenzene;1-Chloro-2,6-dinitro-4-(trifluoromethyl)benzene;4-Chloro-α,α,α-trifluoro-3,5-dinitrotoluene;1,3-Dinitro-2-chloro-5-(trifluoromethyl)benzene;Chloralin;NSC 88274;3,5-Dinitro-4-chlorotrifluoromethylbenzene

393-75-9

C7H2ClF3N2O4

InChIKey=HFHAVERNVFNSHL-UHFFFAOYSA-N

270.55

270.55

1220937

206-889-3

T97IUB50MN

88274

2811

DTXSID8024781

29049085

Organic Fluorine Compound

91.6

2.64

4-chloro-3,5-dinitro-alpha,alpha,alpha-trifluorotoluene appears as yellow crystals. (NTP, 1992)

1.7±0.1 g/cm3

57 °C

>250°C

126°C

1.533

Insoluble in water.

Store below +30°C.

Oral-Rat  LD50: 930 mg/kg

Combustible; Fire site decomposes toxic nitrogen oxides; Fluoride and chloride fumes

No rapid reaction with air. No rapid reaction with water.

Nitro, Nitroso, Nitrate, and Nitrite Compounds, Organic

A halogenated aromatic nitro compound. Aromatic nitro compounds range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation. The aromatic nitro compounds may explode in the presence of a base such as sodium hydroxide or potassium hydroxide even in the presence of water or organic solvents. The explosive tendencies of aromatic nitro compounds are increased by the presence of multiple nitro groups.