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Merck
CN

235814

2,4-二氯-5-硝基三氟甲基苯

97%

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线性分子式:
Cl2C6H2(NO2)CF3
化学文摘社编号:
分子量:
260.00
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
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产品名称

2,4-二氯-5-硝基三氟甲基苯, 97%

InChI

1S/C7H2Cl2F3NO2/c8-4-2-5(9)6(13(14)15)1-3(4)7(10,11)12/h1-2H

SMILES string

[O-][N+](=O)c1cc(c(Cl)cc1Cl)C(F)(F)F

InChI key

VLVNHMVSVDVAOA-UHFFFAOYSA-N

assay

97%

form

solid

mp

55-57 °C (lit.)

functional group

chloro
fluoro
nitro

Application

2,4-Dichloro-5-nitrobenzotrifluoride has been used in the synthesis of:
  • 2-substituted 3,7,8-trichlorodibenzo-p-dioxins
  • new substituted 10 H-phenothiazines

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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分析证书(COA)

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M Romkes et al.
Cancer research, 47(19), 5108-5111 (1987-10-01)
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-tetrachlorodibenzo-p-dioxin as the radioligand. Multiple parameter linear regression analysis of the binding data from the four species gave
Naveen Gautam et al.
Nucleosides, nucleotides & nucleic acids, 29(3), 178-189 (2010-04-22)
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-acetyl-2,3,5-tri-O-benzoyl-beta-ribofuranose). On oxidation with hydrogen peroxide in glacial acetic acid

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