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235814

2,4-Dichloro-5-nitrobenzotrifluoride

Name: 2,4-Dichloro-5-nitrobenzotrifluoride
Brand: ALDRICH

97%

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About This Item

Linear Formula:

Cl₂C₆H₂(NO₂)CF₃

CAS Number:

400-70-4

Molecular Weight:

260.00

NACRES:

NA.22

PubChem Substance ID:

24854002

UNSPSC Code:

12352100

MDL number:

MFCD00007073

Assay:

97%

Form:

solid

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Properties

assay

97%

form

solid

mp

55-57 °C (lit.)

functional group

chloro, fluoro, nitro

SMILES string

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

InChI

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

InChI key

VLVNHMVSVDVAOA-UHFFFAOYSA-N

Description

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

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number

0409CL

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

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

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.

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

Global Trade Item Number

SKU	GTIN
235814-25G	04061832098999