dimethyl amine
1,1,1,3,3,3-hexamethyl-disilazane
N,N-Dimethyltrimethylsilylamine
Conditions | Yield |
---|---|
With 1,3-dimethyl-2-imidazolidinone at 40℃; Reagent/catalyst; | 94% |
With ammonium sulfate at 80℃; for 8h; Reagent/catalyst; Time; Autoclave; | 84% |
trimethylsilyl <(dimethylamino)methyl>methylcarbamate
A
1,3,5-trimethyl-1,3,5-triazacyclohexane
B
N,N-Dimethyltrimethylsilylamine
Conditions | Yield |
---|---|
at 20℃; for 360h; nitrogen atmosphere; | A 90% B n/a |
bis-(dimethylamino)methane
bis(trimethylsilyl) 2-(2-furyl)ethylphosphonite
A
N,N-Dimethyltrimethylsilylamine
Conditions | Yield |
---|---|
With zinc(II) chloride at 130℃; for 1h; | A n/a B 83% |
benzylthiotrimethylsilane
N,N-dimethylphenylmethane sulfenamide
A
dibenzyl disulphide
B
N,N-Dimethyltrimethylsilylamine
Conditions | Yield |
---|---|
at 80 - 110℃; | A 72% B 79% |
trimethylsilyl iodide
N,N-dimethyl acetamide
A
N,N-Dimethyltrimethylsilylamine
B
heptamethyldisilazane
C
N-methyldiacetamide
D
methyl iodide
Conditions | Yield |
---|---|
In dichloromethane at 35℃; for 5h; | A 76% B 1% C 5% D 3% |
Conditions | Yield |
---|---|
In methylbutane Ambient temperature; | 75% |
In octane; acetonitrile at 20℃; for 5h; Solvent; Reflux; | 70% |
bis-(dimethylamino)methane
bis(trimethylsilyl) [2-(2-furyl)-1-(trimethylsilyloxycarbonyl)ethyl]phosphonite
A
N,N-Dimethyltrimethylsilylamine
B
trimethylsilyl (dimethylaminomethyl)[2-(2-furyl)-1-(trimethylsiloxycarbonyl)ethyl]phosphinate
Conditions | Yield |
---|---|
With zinc(II) chloride at 110 - 130℃; for 1.5h; | A n/a B 74% |
A
N,N-Dimethyltrimethylsilylamine
B
dipropylphosphinous iodide
Conditions | Yield |
---|---|
With trimethylsilyl iodide In chlorobenzene at 110 - 132℃; for 8h; | A n/a B 63% |
trimethylsilyl iodide
N,N-dimethyl-formamide
A
N,N-Dimethyltrimethylsilylamine
B
N-formyl-N-methylformamide
C
N-Methyl-N-(trimethylsilyl)-formamid
D
formyl iodide
E
methyl iodide
Conditions | Yield |
---|---|
In dichloromethane at 40℃; for 5h; | A 61% B 1% C 11% D 5% E 11% |
trimethylsilyl iodide
Hexamethylphosphorous triamide
A
N,N-Dimethyltrimethylsilylamine
B
N,N,N',N'-tetramethylphosphorodiamidous iodide
Conditions | Yield |
---|---|
In dichloromethane Ambient temperature; | A n/a B 60% |
bis-(dimethylamino)methane
C7H19PS4Si
A
N,N-Dimethyltrimethylsilylamine
Conditions | Yield |
---|---|
at 100℃; for 1h; | A 57% B n/a |
at 90 - 100℃; |
methyl-bis(dimethylamino)phosphine
trimethylsilylazide
A
N,N-Dimethyltrimethylsilylamine
B
N-trimethylsilyl-methylbis(dimethylaminophosphine) imine
C
C11H33N5P2Si
Conditions | Yield |
---|---|
at 100℃; for 16h; | A n/a B 45% C 8.0 g |
at 100℃; for 16h; | A n/a B 45% C 20% |
at 100℃; for 16h; | A n/a B 45% C 8 g |
N-(trimethylsilylmethyl)methylamine
N,N-Dimethyltrimethylsilylamine
Conditions | Yield |
---|---|
With n-butyllithium; hexane In tetrahydrofuran; benzene at 20.4 - 50.3℃; Kinetics; |
trimethylsilyl bromide
Hexamethylphosphorous triamide
A
N,N-Dimethyltrimethylsilylamine
B
Brom-bis-dimethylamino-phosphan
Conditions | Yield |
---|---|
Ambient temperature; |
trimethylsilyl fluoride
bis(dimethylamino)dimethylsilane
Dimethyl-N-dimethylamino-fluor-silan
A
dimethyldifluorosilane
B
N,N-Dimethyltrimethylsilylamine
Conditions | Yield |
---|---|
at 120℃; Equilibrium constant; |
trimethylsilyl fluoride
bis(dimethylamino)dimethylsilane
A
dimethyldifluorosilane
B
N,N-Dimethyltrimethylsilylamine
C
Dimethyl-N-dimethylamino-fluor-silan
Conditions | Yield |
---|---|
at 120℃; Equilibrium constant; |
chloro-trimethyl-silane
Tetrakis(dimethylamino)methan
A
N,N-Dimethyltrimethylsilylamine
B
N,N,N',N',N'',N''-hexamethylguanidinium chloride
Conditions | Yield |
---|---|
In toluene 0 deg C to r.t., overnight; Yield given; |
chloro-trimethyl-silane
N,N-dimethylammonium chloride
N,N-Dimethyltrimethylsilylamine
Conditions | Yield |
---|---|
With triethylamine; sodium iodide In acetonitrile for 0.5h; Ambient temperature; Yield given; |
B2F4(N(CH3)2Si(CH3)3)
A
N,N-Dimethyltrimethylsilylamine
B
diboron tetrafluoride
Conditions | Yield |
---|---|
In neat (no solvent) during heating of B2F4*NMe2SiMe3; |
N,N-Dimethyltrimethylsilylamine
S-Trifluormethyldifluorosulfonium(IV) Hexafluoroarsenat
Bis(dimethylamino)(trifluormethyl)sulfonium-hexafluoroarsenat
Conditions | Yield |
---|---|
-80 deg C -> RT; | 100% |
N,N-Dimethyltrimethylsilylamine
Triphenyl-((E)-(2R,3S)-2,4,6-trimethyl-3-trimethylsilanyloxy-hept-4-enyl)-phosphonium; iodide
Conditions | Yield |
---|---|
In dichloromethane | 100% |
N,N-Dimethyltrimethylsilylamine
chlorodimethylarsenium trifluoromethanesulfonate
bis(dimethylamino)arsenium trifluoromethanesulfonate
Conditions | Yield |
---|---|
100% |
N,N-Dimethyltrimethylsilylamine
chlorodiethylarsenium trifluoromethanesulfonate
diethylaminodimethylaminoarsenium trifluoromethanesulfonate
Conditions | Yield |
---|---|
100% |
Conditions | Yield |
---|---|
In diethyl ether for 15h; Ambient temperature; | 100% |
N,N-Dimethyltrimethylsilylamine
4-[4-(2-iodo-benzyl)-piperazin-1-yl]-cyclohexanone
{4-[4-(2-iodo-benzyl)-piperazin-1-yl]-cyclohex-1-enyl}-dimethyl-amine
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid | 100% |
N,N-Dimethyltrimethylsilylamine
4-[4-(2,5-difluoro-benzyl)-piperidin-1-yl]-cyclohexanone
{4-[4-(2,5-difluoro-benzyl)-piperidin-1-yl]-cyclohex-1-enyl}-dimethyl-amine
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid | 100% |
{bis(trimethylsilyl)amino}-t-butylchloroborane
N,N-Dimethyltrimethylsilylamine
(tert-butyl)[bis(trimethylsilyl)amino](dimethylamino)borane
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: Me3SiCl; under N2, equimolar amt. of Me3SiNMe2 was added to stirred (Me3Si)2NB(C(CH3)3)Cl at 0°C, warmed to room temp., stirred overnight; elem. anal.; | 100% |
N,N-Dimethyltrimethylsilylamine
S-(Perfluorethyl)thiazyldifluorid
A
trimethylsilyl fluoride
B
S-(Dimethylamino)-S-(perfluorethyl)thiazylfluorid
Conditions | Yield |
---|---|
for 72h; -30 deg C to RT; | A n/a B 99% |
Conditions | Yield |
---|---|
With 2,4,6-trichloroborazine In dichloromethane at 20℃; | 99% |
N,N-Dimethyltrimethylsilylamine
(R)-3-hydroxy-5-phenyl-pentanoic acid ethyl ester
(3R)-ethyl 5-phenyl-3-trimethylsilyloxy-pentanoate
Conditions | Yield |
---|---|
at 20℃; for 16h; | 99% |
for 16h; |
N,N-Dimethyltrimethylsilylamine
Conditions | Yield |
---|---|
In chloroform at 20℃; for 1h; | 99% |
B,B',B''-trichloroborazine
N,N-Dimethyltrimethylsilylamine
2,4,6-tris(dimethylamino)borazene
Conditions | Yield |
---|---|
In dichloromethane (Ar or N2), ligand in CH2Cl2 added slowly at -78°C to borazine inCH2Cl2, warmed to room temp.; evapd.(vac.), crystd. twice (CH2Cl2); | 99% |
N,N-Dimethyltrimethylsilylamine
5-chloro-5H-dibenzo[a,d]cycloheptene
(5-H-dibenzo[a,d]cyclohepten-5-yl)-dimethylamine
Conditions | Yield |
---|---|
In toluene Inert atmosphere; | 99% |
N,N-Dimethyltrimethylsilylamine
((C5(CH3)5)Fe(C5H4))2BBr
((C5(CH3)5)Fe(C5H4))2BN(CH3)2
Conditions | Yield |
---|---|
In toluene (N2) Me3SiNMe2 was added at room temp. to soln. Fe complex in toluene and stirred for 1 h; volatiles were removed in vacuo; elem. anal.; | 99% |
Pyridine-3-sulfonyl chloride
N,N-Dimethyltrimethylsilylamine
Conditions | Yield |
---|---|
In acetonitrile for 1h; Reflux; Inert atmosphere; | 99% |
N,N-Dimethyltrimethylsilylamine
dabsyl chloride
4-(4-(dimethylamino)diazenyl)-N,N-dimethylbenzenesulfonamide
Conditions | Yield |
---|---|
In acetonitrile for 1h; Reflux; Inert atmosphere; | 99% |
N,N-Dimethyltrimethylsilylamine
cyclopropanesulfonyl chloride
Conditions | Yield |
---|---|
In acetonitrile for 1h; Reflux; Inert atmosphere; | 99% |
N,N-Dimethyltrimethylsilylamine
dansyl chloride
5-(dimethylamino)-N,N-dimethylnaphthalene-2-sulfonamide
Conditions | Yield |
---|---|
In acetonitrile for 1h; Reflux; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With titanium tetrachloride In toluene at 55℃; for 17h; | 99% |
6-methoxy-3-pyridinecarboxaldehyde
N,N-Dimethyltrimethylsilylamine
3-methoxy-1-iodobenzene
Conditions | Yield |
---|---|
Stage #1: 6-methoxy-3-pyridinecarboxaldehyde; N,N-Dimethyltrimethylsilylamine With t-butyldimethylsiyl triflate In 1,4-dioxane for 0.05h; Inert atmosphere; Glovebox; Stage #2: 3-methoxy-1-iodobenzene With nickel(II) bromide dimethoxyethane; 2,6-bis(pyrazole)pyridine; zinc In 1,4-dioxane at 50℃; for 24h; Inert atmosphere; Sealed tube; | 99% |
Conditions | Yield |
---|---|
With lithium di-1-admantylamide In diethyl ether; cyclohexane at 50℃; for 24h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 0.5h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With titanium tetrachloride | 99% |
pyridine-4-carbaldehyde
N,N-Dimethyltrimethylsilylamine
A
Hexamethyldisiloxane
B
(bis-dimethylamino methyl)-4 pyridine
Conditions | Yield |
---|---|
With bromine; trimethylsilyl trifluoromethanesulfonate In tetrachloromethane for 48h; Ambient temperature; | A n/a B 98% |
3-pyridinecarboxaldehyde
N,N-Dimethyltrimethylsilylamine
A
Hexamethyldisiloxane
B
(bis-dimethylamino methyl)-3 pyridine
Conditions | Yield |
---|---|
With bromine; trimethylsilyl trifluoromethanesulfonate In tetrachloromethane for 18h; Ambient temperature; | A n/a B 98% |
furfural
N,N-Dimethyltrimethylsilylamine
A
(bis-dimethylamino methyl)-2 furanne
B
Hexamethyldisiloxane
Conditions | Yield |
---|---|
With bromine; trimethylsilyl trifluoromethanesulfonate In tetrachloromethane for 4h; Ambient temperature; | A 98% B n/a |
Conditions | Yield |
---|---|
In diethyl ether for 15h; Ambient temperature; | 98% |
N,N-Dimethyltrimethylsilylamine
1-(Phenylsulfonyl)-1,2,3,4-tetrahydro-2-phenyl-4-quinolone
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid at 80℃; for 5h; | 98% |
N,N-Dimethyltrimethylsilylamine
1,3-bis(dibromoboryl)cymantrene
Mn(CO)3C5H3(B(N(CH3)2)2)2
Conditions | Yield |
---|---|
In toluene (N2); dropwise addn. of a soln. of Si compd. in toluene to a soln. of Mncomplex in toluene at room temp., stirring overnight; evapn. in vac., cooling at -40°C for 12 h; | 98% |
IUPAC Name: N-methyl-N-trimethylsilylmethanamine
Molecular Formula: C5H15NSi
Molecular Weight: 117.27g/mol
EINECS: 218-222-3
Chemical Properties: clear colorless to pale yellow liquid
Density: 0.732 g/mL at 25 °C(lit.)
Melting Point: <0°C
Boiling Point: 89.3 °C at 760 mmHg
Solubility: decomposes
liansport Information: UN 2733 3/PG 2
Properties: liquid
Freely Rotating Bonds: 1
Polar Surface Area: 3.24Å2
Index of Refraction: 1.403
Molar Refractivity: 37.65 cm3
Molar Volume: 154 cm3
Polarizability: 14.92 ×10-24 cm3
Surface Tension: 17.6 dyne/cm
Enthalpy of Vaporization: 31.57 kJ/mol
Vapour Pressure: 66.5 mmHg at 25°C
Sensitive moisture sensitive
The chemical synonyms of Dimethylaminotrimethylsilane (2083-91-2) are Dimethylaminotrimethylsilan ; (Dimethylamino)trimethylsilane ; N,N-dimethylaminotrimethylsilane ; N,N-dimethylaminotrimethylsilane tmsdma ; N,N-dimethyltrimethylsilylamine ; N-trimethylsilydimethylamine ; N-(trimethylsilyl)dimethylamine ; Tmsdma .Product categories of Dimethylaminotrimethylsilane (2083-91-2) are Aminosilanes ; Analytical Chemistry ; GC Derivatizing Reagents ; Si (Classes of Silicon Compounds) ; Silicon Compounds (for Synthesis) ; Silylation (GC Derivatizing Reagents) ; Si-N Compounds ; Synthetic Organic Chemistry ; Trimethylsilylation (GC Derivatizing Reagents) .The molecular structure of Dimethylaminotrimethylsilane (2083-91-2) is.
It can be used as raw material in organic synthesis.
Explosive reaction with xenon difluoride below 0°C. When heated to decomposition it emits toxic fumes of NOx.
Hazard Codes: F,C
F: Highly flammable
C: Corrosive
Risk Statements: 11-34
11: Highly flammable
34: Causes burns
Safety Statements: 16-26-36/37/39-45
16: Keep away from sources of ignition - No smoking
26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
36/37/39: Wear suitable protective clothing, gloves and eye/face protection
45: In case of accident or if you feel unwell, seek medical advice immediately (show the label where possible)
F 1-10
HazardClass : 3
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