282278
2,6-Difluorobenzamide
97%
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About This Item
Linear Formula:
F2C6H3C(O)NH2
CAS Number:
Molecular Weight:
157.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-972-8
Beilstein/REAXYS Number:
2047480
MDL number:
Product Name
2,6-Difluorobenzamide, 97%
InChI key
AVRQBXVUUXHRMY-UHFFFAOYSA-N
InChI
1S/C7H5F2NO/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3H,(H2,10,11)
SMILES string
NC(=O)c1c(F)cccc1F
assay
97%
form
solid
mp
145-148 °C (lit.)
solubility
ethanol: soluble 5%, clear to turbid, colorless to light yellow
functional group
amide
fluoro
Quality Level
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General description
2,6-Difluorobenzamide is a major metabolite of pesticide diflubenzuron and has been quantitated by HPLC/diode-array method.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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HPLC/diode-array method for the determination of the pesticide diflubenzuron and its major metabolites 2,6-difluorobenzamide, 4-chlorophenylurea, and 4-chloroaniline in forestry matrixes.
Rodriguez E, et al.
Journal of Liquid Chromatography and Related Technologies, 21(12), 1857-1870 (1998)
J Koerts et al.
Xenobiotica; the fate of foreign compounds in biological systems, 27(8), 801-817 (1997-08-01)
1. The metabolic fate of the insecticide teflubenzuron, orally dosed to the male Wistar rat, was investigated. Particular attention was paid to the metabolic fate of the benzoyl and aniline moiety after hydrolysis of the urea bridge. 2. The 0-48-h
C Eriksson et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 30(10), 871-877 (1992-10-01)
The herbicides dichlobenil (2,6-dichlorobenzonitrile), chlorthiamid (2,6-dichlorothiobenzamide) and their environmental degradation product 2,6-dichlorobenzamide are irreversibly bound and toxic to the olfactory mucosa following single injections in mice (Brandt et al., Toxicology and Applied Pharmacology 1990, 103, 491-501; Brittebo et al., Fundamental
Varahenage R Perera et al.
Biochimica et biophysica acta, 1840(9), 2851-2861 (2014-05-14)
Gram-positive bacteria in the phylum Firmicutes synthesize the low molecular weight thiol bacillithiol rather than glutathione or mycothiol. The bacillithiol transferase YfiT from Bacillus subtilis was identified as a new member of the recently discovered DinB/YfiT-like Superfamily. Based on structural
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