Conditions | Yield |
---|---|
With sulfuric acid; sulfur dioxide; potassium iodide In water for 3h; | 76% |
With sulfuric acid; sulfur dioxide; potassium iodide | |
With hydrogenchloride; sulfur dioxide; potassium iodide | |
Multistep reaction; | |
With sulfuric acid; sulfur dioxide; potassium iodide In water |
Conditions | Yield |
---|---|
With hydrogenchloride; sulfur dioxide; potassium iodide In water for 2h; | 54% |
triphenyl phosphite
A
dimethyliodoarsine
B
O,O,O-triphenyl phosphorothioate
Conditions | Yield |
---|---|
In chloroform-d1 for 6h; | A 22% B n/a |
Conditions | Yield |
---|---|
With ethanol; potassium iodide unter Luftausschluss; | |
With acetone; sodium iodide unter Luftausschluss; |
Conditions | Yield |
---|---|
With hydrogen iodide bei der Destillation; |
Conditions | Yield |
---|---|
Zersetzt sich beim Erhitzen; |
tetramethyldiarsine
methyl iodide
A
dimethyliodoarsine
B
tetramethylarsonium iodide
Conditions | Yield |
---|---|
analog reagiert Aethyljodid; |
Conditions | Yield |
---|---|
With sodium hydroxide; ethanol und reduziert das Reaktionsprodukt in salzsaurer Loesung mit Schwefeldioxyd; | |
With sodium hydroxide anschliessend mit wss.HCl und SO2; |
Conditions | Yield |
---|---|
With arsenic |
Conditions | Yield |
---|---|
With hydrogen iodide In dichloromethane |
Conditions | Yield |
---|---|
With Iodine monochloride |
dimethyliodoarsine
Conditions | Yield |
---|---|
bei der Destillation; |
Dimethylarsinic acid
hydrogen iodide
A
dimethyliodoarsine
B
water
C
iodine
methyl iodide
A
dimethyliodoarsine
B
arsenic triiodide
C
tetramethylarsonium iodide
D
methyldiiodoarsine
Conditions | Yield |
---|---|
In not given reaction of CH3I with amorphous As at room temperature;; |
cacodyl sulfide
dimethyl iodoborane
A
dimethyliodoarsine
B
(CH3)2AsSB(CH3)2
triphenylphosphine
A
dimethyliodoarsine
B
dimethylarsino dimethyldithioarsinate
C
triphenylphosphine sulfide
Conditions | Yield |
---|---|
In chloroform-d1 for 1h; |
Conditions | Yield |
---|---|
In melt Mn2(CO)8Cl2 in ampoule cooled to -196 °C, (CH3)2AsI added, held at 60 °C 4 h, cooled to room temp.; sublimated in vac., elem. anal.; | 100% |
pentacarbonylchloromanganese(I)
dimethyliodoarsine
Mn(CO)4Cl(As(CH3)2I)
Conditions | Yield |
---|---|
In melt byproducts: CO; Mn(CO)5Cl in ampoule cooled to -196 °C, (CH3)2AsI added, held at 60 °C 4 h, cooled to room temp.; sublimated in vac., elem. anal.; | 100% |
iodo(pentacarbonyl)manganese(I)
dimethyliodoarsine
Mn(CO)4I(As(CH3)2I)
Conditions | Yield |
---|---|
In melt byproducts: CO; Mn(CO)5I in ampoule cooled to -196 °C, (CH3)2AsI added, held at 80 °C 4 h, cooled to room temp.; sublimated in vac., elem. anal.; | 100% |
bromopentacarbonylmanganese(I)
dimethyliodoarsine
Mn(CO)4Br(As(CH3)2I)
Conditions | Yield |
---|---|
In melt byproducts: CO; Mn(CO)5Br in ampoule cooled to -196 °C, (CH3)2AsI added, held at 70 °C 4 h, cooled to room temp.; sublimated in vac., elem. anal.; | 100% |
Conditions | Yield |
---|---|
In melt Mn2(CO)8I2 in ampoule cooled to -196 °C, (CH3)2AsI added, held at80 °C 4 h, cooled to room temp.; sublimated in vac., elem. anal.; | 100% |
Conditions | Yield |
---|---|
In melt Mn2(CO)8Br2 in ampoule cooled to -196 °C, (CH3)2AsI added, held at 70 °C 4 h, cooled to room temp.; sublimated in vac., elem. anal.; | 100% |
Conditions | Yield |
---|---|
With iodine monofluoride In trichlorofluoromethane 1.) -78 deg C, 15 min, 2.) RT, 30 min; | 95% |
dimethyliodoarsine
3,4,6-tri-O-benzoyl-2-deoxy-1-thio-β-D-arabino-hexopyranose
3,4,6-tri-O-benzoyl-2-deoxy-1-S-dimethylarsino-1-thio-β-D-arabino-hexopyranose
Conditions | Yield |
---|---|
With pyridine In dichloromethane Heating; | 90% |
dimethyliodoarsine
2,2'-bis(dimethylarsinomethyl)-1,1'-binaphthyl
Conditions | Yield |
---|---|
In tetrahydrofuran Ambient temperature; | 90% |
dimethyliodoarsine
Conditions | Yield |
---|---|
In dichloromethane (Ar); addn. of org. compd. to W-complex in CH2Cl2, stirring (-78°C); pptn. on addn. of ether/pentane, recryst. (CH2Cl2/ether/pentane), drying (high vac., room temp.); elem. anal.; | 86% |
dimethyliodoarsine
Carbonyl(η5-cyclopentadienyl)[(dimethylarsino)(4-methylphenyl)keten]iodo(trimethylphosphan)wolfram
Conditions | Yield |
---|---|
In dichloromethane under Ar, dropping of AsI(CH3)2 to the solution of η2-ketenyl complex in dichloromethane at room temp., stirred for 1 h; evapn. in vac., extn. with ether/pentane, recrystn. evapn. in vac., elem. anal.; | 85% |
dimethyliodoarsine
Carbonyl(η5-cyclopentadienyl)[(dimethylarsino)methylketen]iodo(trimethylphosphan)wolfram
Conditions | Yield |
---|---|
In dichloromethane under Ar, dropping of AsI(CH3)2 to the solution of η2-ketenyl complex in dichloromethane at room temp., stirred for 1 h; evapn. in vac., extn. with ether/pentane, recrystn. evapn. in vac., elem. anal.; | 82% |
(tris(2-diphenylphosphinoethyl)amin)Pd
dimethyliodoarsine
sodium tetraphenyl borate
{(N(CH2CH2P(C6H5)2)3)PdAs(CH3)2}(1+)*B(C6H5)4(1-)={(N(CH2CH2P(C6H5)2)3)PdAs(CH3)2}B(C6H5)4
Conditions | Yield |
---|---|
In ethanol; benzene byproducts: NaI; Room temp. reaction of (np3)Pd with equimolar quantities of Me2AsI in benzene-ethanol soln. under a nitrogen atmosphere.; | 80% |
(tris(2-diphenylphosphinoethyl)amin)Pt(PPh3)
dimethyliodoarsine
sodium tetraphenyl borate
{(N(CH2CH2P(C6H5)2)3)PtAs(CH3)2}(1+)*B(C6H5)4(1-)={(N(CH2CH2P(C6H5)2)3)PtAs(CH3)2}B(C6H5)4
Conditions | Yield |
---|---|
In ethanol; benzene byproducts: NaI; Room temp. reaction of (np3)Pt(PPh3) with equimolar quantities of Me2AsI in benzene-ethanol soln. under a nitrogen atmosphere.; | 80% |
(benzene)tricarbonylchromium
dimethyliodoarsine
(η6-phenyl)tricarbonylchromium dimethylarsine
Conditions | Yield |
---|---|
With n-C4H9Li In tetrahydrofuran (Ar); addn. of n-BuLi in hexane to cold soln. of Cr-complex in THF at .-78°C; stirred for 60 min; addn. of Me2AsI in THF; stirred for 60 min at -78°C; slowly warmed to room temp.;; filtration (through SiO2); solvent removed (reduced pressure); crystn. (hexane/CH2Cl2); elem. anal.; | 70% |
With BuLi In tetrahydrofuran; hexane Ar-atmosphere; addn. of 1 equiv. BuLi (in hexane) to Cr-complex (in THF)at -78°C, stirring (-78°C), addn. of arsine, stirring (-7 8°C, then room temp.); evapn., dissoln. in CH2Cl2, filtration, evapn.; elem. anal.; | 70% |
Conditions | Yield |
---|---|
Stage #1: N,N'-dimethylbenzylamine With n-butyllithium In diethyl ether; hexane for 24h; Stage #2: dimethyliodoarsine In diethyl ether for 5h; | 67% |
Stage #1: N,N'-dimethylbenzylamine With n-butyllithium Stage #2: dimethyliodoarsine |
dimethyliodoarsine
sodium
(+/-)-1-Chloro-2-(methylphenylphosphino)benzene
Conditions | Yield |
---|---|
In acetone byproducts: tetramethyldiarsane, methyldiphenylphosphine, methylphenylphosphine; Ar-atmosphere; addn. of Na-foil to Me2AsI (in THF), filtration, addn. to chlorophosphine (-78°C), stirring for 48 h (-20°C), evapn., treatment with CH2Cl2/H2O, evapn. of org. layer, fractional distn., treatment with Ni(ClO4)2 (pptn.); collection, washing (Et2O), drying (vac.); second crop on evapn. of filtrate, extn. into Et2O and addn. of Ni(ClO4)2 (in acetone soln.); elem. anal.; | 67% |
1-diphenylphosphinomethyl-1,2-dicarba-closo-dodecaborane
dimethyliodoarsine
1-dimethylarsino-2-diphenylphosphinomethyl-o-carborane
Conditions | Yield |
---|---|
With hydrogenchloride; n-butyllithium In benzene inert atmosphere; dropwise addn. of BuLi soln. to B-compd., mixt. stirring (1h), Me2AsCl addn., mixt. heating until reaction complete, cooling,treatment with dild. HCl; extn. (ether), extract drying (Na2SO4), evapn., residue chromy. (silicagel); elem. anal.; | 66% |
dimethyliodoarsine
bis-(2-chloroethyl)amine hydrochloride
bis<-2(dimethylarsinoethyl)>amine
Conditions | Yield |
---|---|
In tetrahydrofuran for 3h; | 65% |
dimethyliodoarsine
1,3,4-tri-O-acetyl-2-deoxy-6-thio-β-D-arabino-hexopyranose
1,3,4-tri-O-acetyl-2-deoxy-6-S-dimethylarsino-6-thio-β-D-arabino-hexopyranose
Conditions | Yield |
---|---|
With pyridine In toluene for 1h; Heating; | 65% |
dimethyliodoarsine
B
Fe3(CO)9(μ3-S-t-C4H9)(μ2-As(CH3)2)
Conditions | Yield |
---|---|
In diethyl ether; toluene byproducts: [H3N(t-C4H9)]I; under N2, Fe complex dissolved at 20°C in Et2O, treated with toluene, Me2AsI added, stirred for 1 h at room temp.; SiO2 added, dried in high vac., chromd. (SiO2, -20°C, n-pentane/toluene), evapd., recrystd. from toluene at -30°C; elem. anal.; | A n/a B 64% |
1-{(dimethylarsino)methyl}-o-carbaborane
dimethyliodoarsine
1-(dimethylarsino)-2-[(dimethylarsino)methyl]-o-carbaborane
Conditions | Yield |
---|---|
With hydrogenchloride; n-butyllithium In benzene inert atmosphere; dropwise addn. of BuLi soln. to B-compd., mixt. stirring (1h), Ph2PCl addn., mixt. heating until reaction complete, cooling, treatment with dild. HCl; extn. (ether), extract drying (Na2SO4), evapn., residue chromy. (silicagel); elem. anal.; | 62% |
dimethyliodoarsine
C8H20Li4N4P4
2,4,6,8-Tetrakis-dimethylarsanylmethyl-2,4,6,8-tetramethyl-2λ5,4λ5,6λ5,8λ5-[1,3,5,7,2,4,6,8]tetrazatetraphosphocine
Conditions | Yield |
---|---|
With potassium fluoride In diethyl ether at -78℃; for 0.166667h; | 55% |
Conditions | Yield |
---|---|
With sodium In tetrahydrofuran at 35℃; for 60h; | 51% |
dimethyliodoarsine
(R)-2,3-dibenzyloxypropyl 5-bromo-5-deoxy-2,3-O-isopropylidene-β-D-riboside
(R)-2,3-dibenzyloxypropyl 5-deoxy-5-dimethylarsino-2,3-O-isopropylidene-β-D-riboside
Conditions | Yield |
---|---|
Stage #1: dimethyliodoarsine With sodium In tetrahydrofuran at 20℃; for 1.5h; Stage #2: (R)-2,3-dibenzyloxypropyl 5-bromo-5-deoxy-2,3-O-isopropylidene-β-D-riboside In tetrahydrofuran for 1h; | 41% |
dimethyliodoarsine
(R)-2,3-dibenzyloxypropyl 5-chloro-5-deoxy-2,3-O-isopropylidene-β-D-riboside
(R)-2,3-dibenzyloxypropyl 5-deoxy-5-dimethylarsino-2,3-O-isopropylidene-β-D-riboside
Conditions | Yield |
---|---|
Stage #1: dimethyliodoarsine With sodium In tetrahydrofuran at 20℃; for 1.5h; Stage #2: (R)-2,3-dibenzyloxypropyl 5-chloro-5-deoxy-2,3-O-isopropylidene-β-D-riboside In tetrahydrofuran for 3h; | 41% |
(R)-N,N-dimethyl-1-ferrocenylethylamine
dimethyliodoarsine
Conditions | Yield |
---|---|
With n-butyllithium In diethyl ether the amine was stirred with n-BuLi in diethyl ether for 1.5 h, then the halide was added and stirred for 3 h; aq. slurry of NaHCO3 was added and stirred for 1 h before filtration. the ppt. was washed with ether, the filtrate and washings were washed with water, the organic layer was dried over K2CO3 and evapd., then chromd.; elem. anal.; | 40% |
Conditions | Yield |
---|---|
In diethyl ether reaction at 20°C, 2 hours;; | 35% |
In diethyl ether reaction at 20°C, 2 hours;; | 35% |
IUPAC Name: Iodo(dimethyl)arsane
Synonyms of Iododimethylarsine (CAS NO.676-75-5) : Arsinous iodide, As,As-dimethyl- ; Dimethylarsinous iodide ; Arsine, iododimethyl- ; Dimethylarsenic iodide ; Iododimethylarsine
CAS NO:676-75-5
Molecular Formula:C2H6AsI
Molecular Weight :231.8951
Molecular Structure :
EINECS: 211-630-2
Flash Point: 45.1 °C
Enthalpy of Vaporization: 35.56 kJ/mol
Boiling Point: 133.4 °C at 760 mmHg
Vapour Pressure: 10.4 mmHg at 25°C
Arsenic and its compounds are on the Community Right-To-Know List.
Iododimethylarsine (CAS NO.676-75-5) is incompatible with air. Residue from distillation explodes at 72°C. When Iododimethylarsine (CAS NO.676-75-5) is heated to decomposition, it emits toxic fumes of As and I−. See also ARSENIC COMPOUNDS, IODIDES, and ACETYLENE COMPOUNDS and ALKYNES.
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