1,1,2,2-tetrachloro-1,2-dimethyldisilane
A
Dichloromethylsilane
B
Methyltrichlorosilane
Conditions | Yield |
---|---|
silica gel; 3,5-Dimethyl-1-<(2-triethoxysilyl)ethyl>-1H-pyrazol Product distribution; Mechanism; Heating; var. of catalyst, also with HCl; | A 0.4% B 99.6% |
Conditions | Yield |
---|---|
With hydrogenchloride In diethyl ether at 80℃; for 36h; Temperature; Solvent; Reagent/catalyst; | A 7% B 87% |
With hydrogenchloride In 1,4-dioxane at 100℃; for 49.33h; Time; | A 87% B 9% |
With HCl In neat (no solvent) heating of CH3SiH3 and HCl in a closed tube at 100°C in presence of AlCl3 for several hours;; | |
With hydrogenchloride; diethyl ether In benzene-d6 at 80℃; Reagent/catalyst; Schlenk technique; Inert atmosphere; | A 7 %Spectr. B 87 %Spectr. |
methylene chloride
silicon
A
Dichloromethylsilane
B
Methyltrichlorosilane
C
dimethylsilicon dichloride
Conditions | Yield |
---|---|
tin; aluminum silicide; zinc(II) oxide; copper dichloride at 280 - 300℃; for 6h; Rochow reaction; | A 1.7% B n/a C 83.8% |
zinc(II) oxide; copper dichloride at 280 - 300℃; for 6h; Rochow reaction; | A 4.5% B n/a C 83.7% |
zinc(II) oxide; aluminium; copper dichloride at 280 - 300℃; for 6h; Rochow reaction; | A 2.8% B n/a C 82.1% |
With PdSi at 400℃; for 6h; |
Methyltrichlorosilane
1,1,2,2-tetrachloro-1,2-dimethyldisilane
A
Dichloromethylsilane
B
chloro-methyl-silane
Conditions | Yield |
---|---|
With tetra-n-butylphosphonium chloride; lithium hydride In diethylene glycol dimethyl ether at -196 - 160℃; for 35h; Reagent/catalyst; Sealed tube; | A 64% B 24% |
With tetra-n-butylphosphonium chloride; lithium hydride In diethylene glycol dimethyl ether at -196 - 160℃; Temperature; Reagent/catalyst; Sealed tube; | A 64 %Spectr. B 24 %Spectr. |
Conditions | Yield |
---|---|
With tetra-n-butylphosphonium chloride; lithium hydride In diethylene glycol dimethyl ether at -196 - 160℃; for 62h; Temperature; Reagent/catalyst; Sealed tube; | A 63% B 19% |
With lithium hydride; triphenylphosphine In diethylene glycol dimethyl ether at -196 - 160℃; for 62h; Time; Reagent/catalyst; Temperature; Sealed tube; | A 62% B 23% |
With Dichlorosilane; Aliquat 336 at 70℃; under 1650.17 Torr; Product distribution / selectivity; | |
With Dichlorosilane; 1-butyl-3-methylimidazolium chloride at 80℃; under 1500.15 Torr; Product distribution / selectivity; | |
With tetra-n-butylphosphonium chloride; lithium hydride at -196 - 120℃; for 2.5h; Time; Temperature; Sealed tube; |
Methyltrichlorosilane
A
Dichloromethylsilane
B
methylsilane
C
chloro-methyl-silane
Conditions | Yield |
---|---|
With Tetraethylene glycol dimethyl ether; tetra-n-butylphosphonium chloride; lithium hydride In 1,4-dioxane at -196 - 120℃; for 70.75h; Temperature; Reagent/catalyst; Sealed tube; | A 60% B 5% C 32% |
With tri-n-butyl-tin hydride; [2,2]bipyridinyl In diethylene glycol dimethyl ether for 1h; Ambient temperature; | A n/a B n/a C 55% |
With Tetraethylene glycol dimethyl ether; tetra-n-butylphosphonium chloride; lithium hydride In 1,4-dioxane at -196 - 120℃; for 70.75h; Sealed tube; | A 40% B 15% C 44% |
dimethylmonochlorosilane
dimethylsilicon dichloride
A
Dichloromethylsilane
B
chloro-trimethyl-silane
C
Methyltrichlorosilane
D
chloro-methyl-silane
Conditions | Yield |
---|---|
With aluminium trichloride at 140℃; for 15h; | A 0.092 mol B 59% C 0.01 mol D 0.055 mol |
Conditions | Yield |
---|---|
With Tetraethylene glycol dimethyl ether; tetra-n-butylphosphonium chloride; lithium hydride In 1,4-dioxane at -196 - 160℃; for 26h; Reagent/catalyst; Sealed tube; | 57% |
With hydrogen; aluminium at 450℃; | |
With trichlorosilane; chlorosilane; Dichlorosilane; tetra-n-butylphosphonium chloride at 78℃; under 1425.14 Torr; Product distribution / selectivity; |
methylene chloride
A
Dichloromethylsilane
B
Methyltrichlorosilane
C
dimethylsilicon dichloride
Conditions | Yield |
---|---|
With silicon; zinc at 325℃; for 24h; Reagent/catalyst; Inert atmosphere; | A n/a B n/a C 41.1% |
With copper(II) oxide; silicon; zinc at 325℃; for 24h; Reagent/catalyst; Inert atmosphere; | A n/a B n/a C 17.5% |
With silicon; bronze; cesium chloride; copper(l) chloride at 200 - 360℃; for 8h; Product distribution / selectivity; |
Conditions | Yield |
---|---|
With Si-Cu; HCl In neat (no solvent) Si-Cu (10:2) and a mixt. of CH4 and HCl at 350°C;; | A 38.8% B 9.4% |
With hydrogenchloride; copper; silicon In neat (no solvent) Si-Cu (10:2) and a mixt. of CH4 and HCl at 350°C;; | A 38.8% B 9.4% |
trimethylsilyl(dimethylchlorosilyl)methane
bis(chlorodimethylsilyl)methane
dichloro[(chlorodimethylsilyl)methyl]methylsilane
bis(methyldichlorosilyl)methane
dimethylsilicon dichloride
A
Dichloromethylsilane
B
dimethylmonochlorosilane
C
methylsilane
D
dimethylsilane
E
chloro-methyl-silane
Conditions | Yield |
---|---|
With tetra-n-butylphosphonium chloride; lithium hydride In diethylene glycol dimethyl ether at -196 - 220℃; for 31h; Sealed tube; | A 7% B 34% C 9% D 5% E 7% |
Methyltrichlorosilane
A
Dichloromethylsilane
B
tetrachlorosilane
C
trichlorosilane
Conditions | Yield |
---|---|
With hydrogen; Rh/C at 700℃; Product distribution / selectivity; | A 5.5% B 28.2% C 22.9% |
Methyltrichlorosilane
dimethylsilicon dichloride
A
Dichloromethylsilane
B
dimethylmonochlorosilane
C
methylsilane
D
chloro-methyl-silane
Conditions | Yield |
---|---|
With Tetraethylene glycol dimethyl ether; tetra-n-butylphosphonium chloride; lithium hydride at 80 - 120℃; for 86.25h; | A 17% B 19% C 11% D 23% |
1,1,1,2,2,2-hexamethyldisilane
pentamethylchlorodisilane
1,2-dichlorotetramethylsilane
1,1,2-trichloro-1,2,2-trimethyldisilane
1,1,2,2-tetrachloro-1,2-dimethyldisilane
1,1-dichlorotetramethyldisilane
A
Dichloromethylsilane
B
chloro-trimethyl-silane
C
Methyltrichlorosilane
D
dimethylmonochlorosilane
E
dimethylsilicon dichloride
Conditions | Yield |
---|---|
With hydrogenchloride at 430 - 750℃; for 72h; Conversion of starting material; | A 4 %Chromat. B 12 %Chromat. C 7 %Chromat. D 6 %Chromat. E 21% |
Methyltrichlorosilane
A
Dichloromethylsilane
B
tetrachlorosilane
Conditions | Yield |
---|---|
With hydrogen; Rh/C at 600℃; Product distribution / selectivity; | A 6.4% B 5.1% |
Conditions | Yield |
---|---|
With aluminium trichloride at 100℃; |
Methyltrichlorosilane
methylsilane
A
Dichloromethylsilane
B
chloro-methyl-silane
Conditions | Yield |
---|---|
With aluminium trichloride | |
With triphenylphosphine In diethylene glycol dimethyl ether at -196 - 120℃; Reagent/catalyst; Solvent; Temperature; Sealed tube; |
Conditions | Yield |
---|---|
With copper; silicon at 300℃; | |
With hydrogenchloride; copper-doped silicon at 300℃; | |
With hydrogen; copper; silicon at 390℃; |
Conditions | Yield |
---|---|
With hydrogenchloride; aluminium trichloride at 100℃; |
Conditions | Yield |
---|---|
With dibutyl ether; trichlorosilane |
methylene chloride
A
Dichloromethylsilane
B
Methyltrichlorosilane
C
dimethylmonochlorosilane
Conditions | Yield |
---|---|
With trichlorosilane; silicon; copper In chloroform at 324.9℃; under 760 Torr; Product distribution; variation of catalists; |
Conditions | Yield |
---|---|
at 100℃; Equilibrium constant; Thermodynamic data; -ΔG; |
allyldichloromethylsilane
benzaldehyde
A
Dichloromethylsilane
B
styrene
C
Methyltrichlorosilane
D
dimethylsilicon dichloride
E
toluene
Conditions | Yield |
---|---|
at 725℃; for 0.00277778h; Product distribution; |
Conditions | Yield |
---|---|
With dihydrogen hexachloroplatinate; trichlorosilane Yield given. Yields of byproduct given; |
Conditions | Yield |
---|---|
With dihydrogen hexachloroplatinate; trichlorosilane Yield given. Yields of byproduct given; |
methylene chloride
buta-1,3-diene
A
1,1-Dichloro-2,5-dihydro-1H-silole
B
Dichloromethylsilane
C
1-chloro-1-methyl-silacyclopent-3-ene
D
Methyltrichlorosilane
E
but-2-enyl-dichloro-methyl-silane
F
dimethylsilicon dichloride
Conditions | Yield |
---|---|
With silicon powder with ca. 4percent copper loading at 291.9℃; Product distribution; Mechanism; |
Methyltrichlorosilane
A
Dichloromethylsilane
B
dimethylmonochlorosilane
C
dimethylsilicon dichloride
Conditions | Yield |
---|---|
With aluminium trichloride; titanium(II) hydride at 300℃; for 20h; Product distribution; var. reaction partners and times; other silicon compounds; | A 0.001 mol B 0.002 mol C 0.02 mol |
methylene chloride
A
Dichloromethylsilane
B
chloro-trimethyl-silane
C
Methyltrichlorosilane
D
dimethylsilicon dichloride
Conditions | Yield |
---|---|
With copper(l) chloride; zinc(II) chloride; silicon at 399.9℃; under 720.06 Torr; Further byproducts given; |
methylene chloride
A
Dichloromethylsilane
B
Methyltrichlorosilane
C
dimethylmonochlorosilane
D
dimethylsilicon dichloride
Conditions | Yield |
---|---|
With copper(l) chloride; zinc(II) chloride; silicon at 399.9℃; under 720.06 Torr; Further byproducts given; |
methane
Dichloromethylsilane
Conditions | Yield |
---|---|
With trichlorosilane at 647.9℃; under 8.5 Torr; Product distribution; Rate constant; Mechanism; other pressures; |
Conditions | Yield |
---|---|
at 90℃; for 5h; Inert atmosphere; | 100% |
at 90℃; for 5h; Inert atmosphere; | 100% |
Stage #1: 1-hexene With diethylenetriaminepentaacetic acid (DTPA)-functionalized silica supported Pt at 60℃; for 0.5h; Stage #2: Dichloromethylsilane at 60℃; for 4h; Catalytic behavior; Temperature; Reagent/catalyst; | 99.6% |
Conditions | Yield |
---|---|
Pt-thiourea Product distribution; Ambient temperature; various catalysts; | 100% |
Pt-thiourea | 100% |
Stage #1: 1-Heptene With diethylenetriaminepentaacetic acid (DTPA)-functionalized silica supported Pt at 60℃; for 0.5h; Stage #2: Dichloromethylsilane at 60℃; for 4h; Reagent/catalyst; | 98.9% |
Conditions | Yield |
---|---|
In hexane at -5℃; | 100% |
In pentane at 0 - 20℃; Inert atmosphere; | 90% |
In pentane at -30 - 20℃; for 24h; Inert atmosphere; | 87% |
In diethyl ether | |
Inert atmosphere; |
Dichloromethylsilane
(4S,5S)-4-<(allyloxy)methyl>-2-methyl-5-phenyloxazol-2-ine
Conditions | Yield |
---|---|
With dihydrogen hexachloroplatinate; isopropyl alcohol for 5h; Heating; | 100% |
Dichloromethylsilane
tetravinylsilane
tetra-2-(dichloromethylsilyl)ethylsilane
Conditions | Yield |
---|---|
dihydrogen hexachloroplatinate In tetrahydrofuran at 20℃; | 100% |
bis(tetrabutylammonium) hexachloroplatinate(IV) In ethanol | 97% |
platinum Addition; |
Dichloromethylsilane
bis-allyloxy-dimethyl-silane
Conditions | Yield |
---|---|
dihydrogen hexachloroplatinate In diethyl ether at 25℃; for 1.25h; | 100% |
Conditions | Yield |
---|---|
dihydrogen hexachloroplatinate In diethyl ether at 25℃; for 3.25h; | 100% |
Conditions | Yield |
---|---|
dihydrogen hexachloroplatinate In diethyl ether at 25℃; for 3.25h; | 100% |
Conditions | Yield |
---|---|
dihydrogen hexachloroplatinate In diethyl ether at 25℃; for 3.25h; | 100% |
Conditions | Yield |
---|---|
dihydrogen hexachloroplatinate In diethyl ether at 25℃; for 1.25h; | 100% |
Dichloromethylsilane
3-[allyloxy-(3-{[3-(bis-allyloxy-methyl-silanyl)-propoxy]-dimethyl-silanyloxy}-propyl)-methyl-silanyloxy]-propene
Conditions | Yield |
---|---|
dihydrogen hexachloroplatinate at 25℃; for 1.25h; | 100% |
Dichloromethylsilane
Conditions | Yield |
---|---|
dihydrogen hexachloroplatinate at 25℃; for 1.25h; | 100% |
Conditions | Yield |
---|---|
bis(tetrabutylammonium) hexachloroplatinate(IV) In ethanol | 100% |
Dichloromethylsilane
Conditions | Yield |
---|---|
chloroplatinic acid 1,1,3,3-tetramethyl-1,3-divinyldisiloxane complex In benzene at 55℃; for 16h; | 100% |
Dichloromethylsilane
Conditions | Yield |
---|---|
chloroplatinic acid 1,1,3,3-tetramethyl-1,3-divinyldisiloxane complex In benzene at 55℃; for 16h; | 100% |
Dichloromethylsilane
tri(allyl)phenylsilane
{tris-[3-(dichloro-methyl-silanyl)-propyl]-silanyl}-benzene
Conditions | Yield |
---|---|
chloroplatinic acid 1,1,3,3-tetramethyl-1,3-divinyldisiloxane complex In benzene at 55℃; for 16h; | 100% |
Dichloromethylsilane
Conditions | Yield |
---|---|
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In 5,5-dimethyl-1,3-cyclohexadiene; diethyl ether at 40℃; for 72h; regioselective reaction; | 100% |
Dichloromethylsilane
Conditions | Yield |
---|---|
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In 5,5-dimethyl-1,3-cyclohexadiene; diethyl ether at 40℃; for 72h; regioselective reaction; | 100% |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; calcium hydride In diethylene glycol dimethyl ether at 50℃; for 7h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
PtCl2*(III)2 In octane at 40 - 45℃; for 8h; Product distribution; examination of regio- and stereo-selectivity of products by catalytic activity; | 99% |
Dichloromethylsilane
Conditions | Yield |
---|---|
platinum on activated charcoal In diethyl ether for 2.5h; Addition; Heating; | 99% |
Conditions | Yield |
---|---|
platinum on activated charcoal In diethyl ether for 2.5h; Addition; Heating; | 99% |
Conditions | Yield |
---|---|
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In toluene at 20℃; for 2h; | 99% |
Conditions | Yield |
---|---|
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In hexane at 60℃; for 4h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In 5,5-dimethyl-1,3-cyclohexadiene at 20℃; for 48h; | 99% |
Conditions | Yield |
---|---|
With bis-triphenylphosphine-palladium(II) chloride In neat (no solvent) at 120℃; for 10h; | 99% |
Conditions | Yield |
---|---|
Stage #1: styrene With Pt loaded on nitrolotriacetic acid-functionalized silica gel at 60℃; for 0.5h; Stage #2: Dichloromethylsilane at 60℃; for 4h; Reagent/catalyst; | 98.8% |
With tetrakis(triphenylphosphine)platinum at 90 - 130℃; for 2h; Reagent/catalyst; Large scale; regiospecific reaction; | 93% |
With N-heterocyclic carbene fuctionalized with methyl(trimethylsilane) and methoxypolyethylene glycol Pt(II) complex at 90℃; for 10h; | 93.7% |
Conditions | Yield |
---|---|
Stage #1: oct-1-ene With diethylenetriaminepentaacetic acid (DTPA)-functionalized silica supported Pt at 60℃; for 0.5h; Stage #2: Dichloromethylsilane at 60℃; for 4h; Reagent/catalyst; | 98.6% |
at 300℃; | |
tetrakis(triphenylphosphine) palladium(0) at 120℃; for 6h; |
Conditions | Yield |
---|---|
With H2PtCl6 | 98.3% |
Product Name: Dichloromethylsilane
The MF of Dichloromethylsilane(75-54-7) is CH4Cl2Si.
The MW of Dichloromethylsilane(75-54-7) is 115.03.
Synonyms: CM8750;dichlorohydridomethylsilicon;dichloromethyl-silan;dichloromethylsilane,[flammableliquid];Methyldichlorosilan;Methyl-dichlorsilan;methyl-dichlorsilan(czech);monomethyldichlorosilane
Product Categories: Chloro;Dichlorosilanes;Si (Classes of Silicon Compounds);Si-Cl Compounds;Si-H Compounds;Chloro Silanes
Mol File: 75-54-7.mol
EINECS: 200-877-1
Enthalpy of Vaporization: 27.14 kJ/mol
Boiling Point: 38.4 °C at 760 mmHg
Vapour Pressure: 468 mmHg at 25°C
MP: -93 °C
Density: 1.105 g/mL at 25 °C(lit.)
Storage temp: 2-8°C
Water Solubility: DECOMPOSES
Sensitive: Air & Moisture Sensitive
CAS DataBase Reference: 75-54-7(CAS DataBase Reference)
NIST Chemistry Reference: 75-54-7(NIST)
EPA Substance Registry System: 75-54-7(EPA Substance)
1. | skn-rbt 2 mg/24H SEV | 85JCAE Prehled Prumyslove Toxikologie; Organicke Latky Marhold, J.,Prague, Czechoslovakia.: Avicenum,1986,1218. | ||
2. | eye-rbt 20 mg/24H MOD | 85JCAE Prehled Prumyslove Toxikologie; Organicke Latky Marhold, J.,Prague, Czechoslovakia.: Avicenum,1986,1218. | ||
3. | orl-rat LD50:2830 µL/kg | JACTDZ Journal of the American College of Toxicology. 12 (1993),572. | ||
4. | ihl-rat LC50:300 ppm/4H | 85JCAE Prehled Prumyslove Toxikologie; Organicke Latky Marhold, J.,Prague, Czechoslovakia.: Avicenum,1986,1218. |
Moderately toxic by inhalation. Corrosive. A severe irritant to skin, eyes, and mucous membranes. Ignites spontaneously in air. A very dangerous fire hazard when exposed to heat or flame. Forms impact-sensitive explosive mixtures with potassium permanganate, lead(II) oxide, lead(IV) oxide, copper oxide, silver oxide. To fight fire, use water, foam, CO2, mist. When heated to decomposition it emits toxic fumes of Cl−. See also CHLOROSILANES.
Safety information of Dichloromethylsilane(75-54-7):
Hazard Codes: F,T,C
Risk Statements: 11-14/15-28-34-37
R11:Highly Flammable ;
R14/15:Reacts violently with water, liberating extremely flammable gases ;
R28:Very Toxic if swallowed ;
R34:Causes burns ;
R37:Irritating to the respiratory system ;
Safety Statements: 16-26-36/37/39-43-45-7/8-30
S16:Keep away from sources of ignition - No smoking ;
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice ;
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection ;
S43:In case of fire, use ... (indicate in the space the precise type of fire-fighting equipment. If water increases the risk add - Never use water) ;
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) ;
S7/8:Keep container tightly closed and dry ;
S30:Never add water to this product ;
RIDADR: UN 1242 4.3/PG 1
WGK Germany: 1
RTECS: VV3500000
F: 10-21
TSCA: Yes
HazardClass: 4.3
PackingGroup: I
Hazardous Substances Data: 75-54-7(Hazardous Substances Data)
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