248010
3,5-Dichloro-2,4,6-trifluoropyridine
98%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C5Cl2F3N
CAS Number:
Molecular Weight:
201.96
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
217-088-3
MDL number:
InChI key
PKSORSNCSXBXOT-UHFFFAOYSA-N
InChI
1S/C5Cl2F3N/c6-1-3(8)2(7)5(10)11-4(1)9
SMILES string
Fc1nc(F)c(Cl)c(F)c1Cl
assay
98%
form
liquid
refractive index
n20/D 1.478 (lit.)
bp
159-160 °C (lit.)
density
1.622 g/mL at 25 °C (lit.)
General description
The solid phase mid FTIR and FT-Raman spectra of 3,5-dichloro-2,4,6-trifluoropyridine has been recorded in the region of 3500-100 cm-1. 3,5-Dichloro-2,4,6-trifluoropyridine reacts with Ni(1,5,-cyclooctadiene)2 in the presence of triethylphosphine (PEt3) to yield trans-Ni(PEt3)2(C5ClF3N)Cl.
Application
3,5-Dichloro-2,4,6-trifluoropyridine has been used in the preparation of Avid AL, an affinity gel designed for the purification of immunoglobulin G.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 1 Inhalation - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
T T Ngo
Journal of chromatography. B, Biomedical applications, 662(2), 351-356 (1994-12-09)
A derivative of aza-arenophilic gel having a dichlorosubstituent and an hydroxy ion as a capping nucleophile has been prepared. The properties of this gel in relation to IgG purification have been investigated in details. In the presence of high salt
V C Lees et al.
Burns : journal of the International Society for Burn Injuries, 18(5), 423-425 (1992-10-01)
An example is reported of a burn caused by cutaneous exposure to 3,5-dichloro 2,4,6-trifluoropyridine (DCTFP) involving 25 per cent of the body surface. A striking feature was the development of the appearance of the burn over the first 72h postinjury.
V Krishnakumar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 61(1-2), 253-260 (2004-11-24)
The solid phase mid FTIR and FT-Raman spectra of 3,5-dibromopyridine (3,5-DBP) and 3,5-dichloro-2,4,6-trifluoropyridine (3,5-DCTFP) have been recorded in the regions 4000-400 cm(-1) and 3500-100 cm(-1), respectively. The spectra were interpreted with the help of normal coordinate analysis (NCA) following full
Xiaoying Hui et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 50(7), 2496-2502 (2012-04-17)
This in vitro study determined the decontamination potential of soap and water, D-TAM skin cleanser, corn oil and the O'Dell reactive skin decontamination system to remove 3,5-dichloro-2,4,6-trifluoropyridine (DCTFP) from human skin after short exposure periods (10 and 30 min). The
Rapid intermolecular carbon-fluorine bond activation of pentafluoropyridine at nickel (0): Comparative reactivity of fluorinated arene and fluorinated pyridine derivatives.
Cronin L, et al.
Organometallics, 16(22), 4920-4928 (1997)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service