2,6-Difluorobenzamide

2,6-Difluorobenzamide Basic information
Product Name:2,6-Difluorobenzamide
Synonyms:2,6-Difluorobenzamide97%;2,6-Difluorbenzamid;2,6-Difluorobenzoylamide;2,6-DIFLUOROBENZAMIDE, 98+%;Fluorine benzaMide 2, 6-2;2,6-difluoro-benzamid;2,6-DIFLUOROBENZAMIDE;2,6-difluorobenzaminde
CAS:18063-03-1
MF:C7H5F2NO
MW:157.12
EINECS:241-972-8
Product Categories:Amides;Carbonyl Compounds;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Organic Building Blocks;intermediate;Aryl Fluorinated Building Blocks;Building Blocks;C7;Carbonyl Compounds;Chemical Synthesis;Fluorinated Building Blocks;Organic Building Blocks;Organic Fluorinated Building Blocks;Other Fluorinated Organic Building Blocks;18063-03-1
Mol File:18063-03-1.mol
2,6-Difluorobenzamide Structure
2,6-Difluorobenzamide Chemical Properties
Melting point 145-148 °C (lit.)
Boiling point 51-52C/15Tor
density 1,199g/cm
refractive index 1,508
storage temp. Sealed in dry,Room Temperature
solubility ethanol: soluble5%, clear to turbid, colorless to light yellow
pka14.54±0.50(Predicted)
form Solid
color Off-White
BRN 2047480
InChIKeyAVRQBXVUUXHRMY-UHFFFAOYSA-N
LogP0.011-0.25 at 25℃
CAS DataBase Reference18063-03-1(CAS DataBase Reference)
NIST Chemistry ReferenceBenzamide, 2,6-difluoro-(18063-03-1)
EPA Substance Registry SystemBenzamide, 2,6-difluoro- (18063-03-1)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-20
Safety Statements 26-37/39-36/37
WGK Germany 1
RTECS CV4355050
HazardClass IRRITANT
HS Code 29242990
Toxicityrat,LC50,inhalation,> 2100mg/m3/4H (2100mg/m3),National Technical Information Service. Vol. OTS0543293,
MSDS Information
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2,6-Difluorobenzamide Usage And Synthesis
Description2,6-Difluorobenzamide is a major metabolite of pesticide diflubenzuron and has been quantitated by HPLC/diode-array method.
Chemical Propertieswhite to yellowish powder
Uses2,6-Difluorobenzamide (CAS# 18063-03-1) is a useful building block used in the synthesis of (E)-3-methyleneisoindolin-1-ones via oxidative annulation acrylates. It is also used in the synthesis of pesticide intermediates, which can be used to produce various insecticides such as fluazuron, chlorpyrifos, and pyrethroids.
Preparation2,6-Difluorobenzamide is obtained by hydrolysis of 2,6-difluorobenzonitrile.
N-(3-amino-4-fluorophenyl)-2,6-difluorobenzamide N-(3-amino-4-methylphenyl)-3,5-difluorobenzamide N-(3-aminopropyl)-2,6-difluorobenzamide N-(3-amino-4-fluorophenyl)-3,5-difluorobenzamide 2,6-DIFLUORO-N-(4-[(4-METHYLPHENYL)SULFONYL]PHENYL)BENZENECARBOXAMIDE 2,6-Difluorobenzoyl hydrazine N-(4-[(4-BROMOPHENYL)SULFANYL]PHENYL)-2,6-DIFLUOROBENZENECARBOXAMIDE N-(3-amino-4-fluorophenyl)-2,4-difluorobenzamide N-(3-bromophenyl)-2,6-difluorobenzamide 2,6-DIFLUORO-3-NITROBENZAMIDE N-PENTAFLUOROBENZOYLIMIDAZOLE 2,6-DIFLUORO-N-(4-[(4-METHYLPHENYL)SULFANYL]PHENYL)BENZENECARBOXAMIDE 2,4,6-TRIFLUOROBENZAMIDE N-(2-aminophenyl)-2,6-difluorobenzamide N-(3-acetylphenyl)-2,6-difluorobenzamide N-(3-amino-2,6-dimethylphenyl)-3,5-difluorobenzamide N-(3-amino-2-methylphenyl)-2,5-difluorobenzamide 4-AMINO-2,3,5,6-TETRAFLUOROBENZAMIDE

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