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2,4-Dichloro-5-nitrobenzotrifluoride

Names

[ CAS No. ]:
400-70-4

[ Name ]:
2,4-Dichloro-5-nitrobenzotrifluoride

[Synonym ]:
Benzene, 1,5-dichloro-2-nitro-4-(trifluoromethyl)-
MFCD00007073
2,4-Dichloro-5-Nitro benzotrifluoride
2,4-Dichloro-5-Nitrobenzotrifluoride
1,5-Dichloro-2-nitro-4-(trifluoromethyl)benzene

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
264.9±35.0 °C at 760 mmHg

[ Melting Point ]:
55-57 °C(lit.)

[ Molecular Formula ]:
C7H2Cl2F3NO2

[ Molecular Weight ]:
259.997

[ Flash Point ]:
114.0±25.9 °C

[ Exact Mass ]:
258.941467

[ PSA ]:
45.82000

[ LogP ]:
3.88

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.511

MSDS

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 ]:
Xn:Harmful;

[ Risk Phrases ]:
R20/21/22;R36/37/38

[ Safety Phrases ]:
S26-S37/39-S36/37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2904909090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2904909090

[ Summary ]:
HS:2904909090 sulphonated, nitrated or nitrosated derivatives of hydrocarbons, whether or not halogenated VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Quantitative structure-activity relationships: analysis of interactions of 2,3,7,8-tetrachlorodibenzo-p-dioxin and 2-substituted analogues with rat, mouse, guinea pig, and hamster cytosolic receptor.

Cancer Res. 47(19) , 5108-5111, (1987)

The competitive receptor binding affinities of thirteen 2-substituted 3,7,8-trichlorodibenzo-p-dioxins to hepatic cytosol from rat, mouse, guinea pig, and hamster were determined with [3H]-2,3,7,8-tet...

Synthesis, spectral characterization, and biological activity of some new substituted 10H-phenothiazines, its ribofuranosides, and sulfones.

Nucleosides Nucleotides Nucleic Acids 29(3) , 178-89, (2010)

This article describes the synthesis of new substituted 10 H-phenothiazines by Smiles rearrangement. These compounds are then used as a base to form ribofuranosides by treating them with a sugar (1-O-...


More Articles


Related Compounds

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