Conditions | Yield |
---|---|
Stage #1: tribromofluoromethane With triphenylphosphine In N,N-dimethyl-formamide for 0.5h; Stage #2: With zinc In N,N-dimethyl-formamide at 20℃; for 0.25h; | 56% |
Conditions | Yield |
---|---|
With mercury(II) fluoride | |
With bromine; antimony(III) fluoride | |
With potassium fluoride; antimony(III) chloride | |
With calcium fluoride; antimony(III) chloride | |
With bromine; antimony(III) fluoride at 110 - 120℃; |
Conditions | Yield |
---|---|
beim Kochen der Loesung; |
dibromofluoromethyltriphenylphosphonium bromide
A
dibromofluoromethane
B
tribromofluoromethane
C
fluorodibromoiodomethane
D
fluorobromodiiodomethane
Conditions | Yield |
---|---|
With potassium fluoride; iodine In various solvent(s) | A 10 % Spectr. B 31 % Spectr. C 57 % Spectr. D 15 % Spectr. |
With potassium fluoride; iodine In various solvent(s) Title compound not separated from byproducts; | A 10 % Spectr. B 31 % Spectr. C 57 % Spectr. D 15 % Spectr. |
dibromofluoromethyltriphenylphosphonium bromide
A
dibromofluoromethane
B
Triphenylphosphine oxide
Conditions | Yield |
---|---|
With water In chloroform for 1h; Mechanism; |
dibromofluoromethane
Conditions | Yield |
---|---|
With bromine at 100℃; |
Bromoform
bromine
antimony(III) fluoride
A
bromodifluoromethane
B
dibromofluoromethane
2,3-Dimethyl-2-butene
diethyl dibromofluoromethylphosphonate
A
dibromofluoromethane
B
diethyl fluorophosphate
C
1-bromo-1-fluoro-2,2,3,3-tetramethylcyclopropane
Conditions | Yield |
---|---|
With potassium fluoride In Triethylene glycol dimethyl ether at 20℃; | A 8 %Spectr. B 93 %Spectr. C 45 %Spectr. |
diethyl dibromofluoromethylphosphonate
A
dibromofluoromethane
B
diethyl fluorophosphate
Conditions | Yield |
---|---|
With potassium fluoride; ethanol In Triethylene glycol dimethyl ether at 20℃; | A 67 %Spectr. B 72 %Spectr. |
dibromofluoromethane
Conditions | Yield |
---|---|
With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride at 20℃; for 72h; Addition; | 94% |
dibromofluoromethane
Conditions | Yield |
---|---|
With sodium hydroxide; ethanol; N-benzyl-N,N,N-triethylammonium chloride In dichloromethane at 20℃; for 72h; | 94% |
dibromofluoromethane
2-vinyl-3-(methoxy)isoindol-1-one
Conditions | Yield |
---|---|
With potassium hydroxide; Bn(n-Bu)3Cl In dichloromethane | 92% |
bicyclohexylidene
dibromofluoromethane
13-Brom-13-fluordispiro<5.0.5.1>tridecan
Conditions | Yield |
---|---|
With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride In dichloromethane for 4h; Ambient temperature; | 90% |
dibromofluoromethane
Conditions | Yield |
---|---|
With potassium hydroxide; 18-crown-6 ether In dichloromethane at 0℃; | 88% |
dibromofluoromethane
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate; potassium hydrogencarbonate In tetrahydrofuran at 20℃; for 18h; Inert atmosphere; Irradiation; | 87% |
dibromofluoromethane
Conditions | Yield |
---|---|
With potassium hydroxide; 18-crown-6 ether In dichloromethane at 20℃; | 86% |
dibromofluoromethane
cyclopropylidenecyclohexane
10-bromo-10-fluorodispiro[2.0.5.1]decane
Conditions | Yield |
---|---|
With ethanol; N-benzyl-N,N,N-triethylammonium chloride; sodium hydroxide In dichloromethane; water at 0 - 20℃; | 86% |
1,1-Diphenylethylene
dibromofluoromethane
(2-bromo-2-fluorocyclopropane-1,1-diyl)dibenzene
Conditions | Yield |
---|---|
With N-benzyl-N,N,N-triethylammonium chloride; sodium hydroxide In dichloromethane at 20℃; | 84% |
With potassium tert-butylate In hexane |
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate; potassium hydrogencarbonate In tetrahydrofuran at 20℃; for 18h; Inert atmosphere; Irradiation; | 83% |
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate In water; N,N-dimethyl-formamide at 20℃; for 18h; Inert atmosphere; Irradiation; | 82% |
dibromofluoromethane
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate In water; N,N-dimethyl-formamide at 20℃; for 18h; Inert atmosphere; Irradiation; | 82% |
dibromofluoromethane
1-ethylcyclohexene
7-Brom-1-ethyl-7-fluorbicyclo<4.1.0>heptan
Conditions | Yield |
---|---|
With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride In dichloromethane for 4h; Ambient temperature; also: 6h, reflux; | 80% |
dibromofluoromethane
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate; potassium hydrogencarbonate In tetrahydrofuran at 20℃; for 18h; Inert atmosphere; Irradiation; | 80% |
dibromofluoromethane
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate In water; N,N-dimethyl-formamide at 20℃; for 18h; Inert atmosphere; Irradiation; | 80% |
dibromofluoromethane
hex-5-en-1-yl 4-bromobenzoate
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate; potassium hydrogencarbonate In tetrahydrofuran at 20℃; for 18h; Inert atmosphere; Irradiation; | 79% |
dibromofluoromethane
Conditions | Yield |
---|---|
With potassium hydroxide; 18-crown-6 ether In dichloromethane at 20℃; | 78% |
Conditions | Yield |
---|---|
With N-benzyl-N,N,N-triethylammonium chloride; sodium hydroxide In dichloromethane; benzene at 20℃; | 78% |
Conditions | Yield |
---|---|
With sodium hydroxide | 78% |
With benzyltrimethylammonium chloride; sodium hydroxide In dichloromethane at 20℃; for 25.5h; | 1.0 g |
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate In water; N,N-dimethyl-formamide at 20℃; for 18h; Inert atmosphere; Irradiation; | 78% |
dibromofluoromethane
hex-5-en-1-yl 4-bromobenzoate
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate In water; N,N-dimethyl-formamide at 20℃; for 18h; Inert atmosphere; Irradiation; | 78% |
dibromofluoromethane
benzoic acid hex-5-enyl ester
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate; potassium hydrogencarbonate In tetrahydrofuran at 20℃; for 18h; Inert atmosphere; Irradiation; | 77% |
dibromofluoromethane
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate In water; N,N-dimethyl-formamide at 20℃; for 18h; Inert atmosphere; Irradiation; | 77% |
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate In water; N,N-dimethyl-formamide at 20℃; for 18h; Inert atmosphere; Irradiation; | 77% |
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate; potassium hydrogencarbonate In tetrahydrofuran at 20℃; for 18h; Inert atmosphere; Irradiation; | 76% |
dibromofluoromethane
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate In water; N,N-dimethyl-formamide at 20℃; for 18h; Inert atmosphere; Irradiation; | 76% |
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate In water; N,N-dimethyl-formamide at 20℃; for 18h; Inert atmosphere; Irradiation; | 76% |
dibromofluoromethane
(hex-5-en-1-yloxy)benzene
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate In water; N,N-dimethyl-formamide at 20℃; for 18h; Inert atmosphere; Irradiation; | 76% |
dibromofluoromethane
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate In water; N,N-dimethyl-formamide at 20℃; for 18h; Inert atmosphere; Irradiation; | 76% |
2-(pent-4-enyl)-isoindoline-1,3-dione
dibromofluoromethane
2-(6-bromo-6-fluorohexyl)isoindoline-1,3-dione
Conditions | Yield |
---|---|
With [4,4’-bis(1,1-dimethylethyl)-2,2’-bipyridine-N1,N1‘]bis [3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-N]phenyl-C]iridium(III) hexafluorophosphate; potassium hydrogencarbonate In tetrahydrofuran at 20℃; for 18h; Inert atmosphere; Irradiation; | 75% |
Molecular Structure of Methane, dibromofluoro-(6CI,7CI,8CI,9CI) (CAS NO.1868-53-7):
Molecular Formula: CHBr2F
Molecular Weight: 191.825
IUPAC Name: Dibromo(fluoro)methane
Synonyms of Methane, dibromofluoro-(6CI,7CI,8CI,9CI) (CAS NO.1868-53-7): Dibromofluoromethane ; Methane, dibromofluoro-
CAS NO: 1868-53-7
Classification Code: Alpha Sort ; BromoVolatiles/ Semivolatiles ; Chemical Class ; D ; DAlphabetic ; DIA - DIC ; Halogenated
Index of Refraction: 1.488
Molar Refractivity: 22.26 cm3
Molar Volume: 77.2 cm3
Surface Tension: 31.5 dyne/cm
Density: 2.483 g/cm3
Enthalpy of Vaporization: 29.67 kJ/mol
Boiling Point: 67.8 °C at 760 mmHg
Vapour Pressure: 155 mmHg at 25°C
Hazard Codes of Methane, dibromofluoro-(6CI,7CI,8CI,9CI) (CAS NO.1868-53-7): Xi,N,Xn,T,F
Risk Statements: 23/24/25-59-22-39-11
R23/24/25: Toxic by inhalation, in contact with skin and if swallowed.
R59: Dangerous to the ozone layer.
R22: Harmful if swallowed.
R39: Danger of very serious irreversible effects.
R11: Highly flammable.
Safety Statements: 24/25-41-59-45-36/37
S24/25: Avoid contact with skin and eyes.
S41: In case of fire and / or explosion do not breathe fumes.
S59: Refer to manufacturer / supplier for information on recovery / recycling.
S45: In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S36/37: Wear suitable protective clothing and gloves.
RIDADR: 2810
Hazard Note: Irritant
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