Product Name

  • Name

    N,N-Dimethyltrimethylsilylamine

  • EINECS 218-222-3
  • CAS No. 2083-91-2
  • Article Data52
  • CAS DataBase
  • Density 0.761 g/cm3
  • Solubility decomposes in water
  • Melting Point <0 °C
  • Formula C5H15NSi
  • Boiling Point 89.3 °C at 760 mmHg
  • Molecular Weight 117.266
  • Flash Point -19 °C
  • Transport Information UN 2733 3/PG 2
  • Appearance clear colorless to pale yellow liquid
  • Safety 16-26-36/37/39-45
  • Risk Codes 11-34
  • Molecular Structure Molecular Structure of 2083-91-2 (N,N-Dimethyltrimethylsilylamine)
  • Hazard Symbols FlammableF, CorrosiveC
  • Synonyms Silanamine,pentamethyl- (9CI);Silylamine, pentamethyl- (6CI,7CI,8CI);(Dimethylamino)trimethylsilane;(N,N-Dimethylamino)trimethylsilane;(Trimethylsilyl)dimethylamine;N,N,1,1,1-Pentamethylsilanamine;N,N-Dimethyl(trimethylsilyl)amine;N,N-Dimethyl-N-(trimethylsilyl)amine;N-(Trimethylsilyl)dimethylamine;N-Methyl-N-(trimethylsilyl)methylamine;Pentamethylsilanamine;Pentamethylsilylamine;TSL 8831;Trimethyl(dimethylamino)silane;
  • PSA 3.24000
  • LogP 1.38290

Synthetic route

dimethyl amine
124-40-3

dimethyl amine

1,1,1,3,3,3-hexamethyl-disilazane
999-97-3

1,1,1,3,3,3-hexamethyl-disilazane

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

Conditions
ConditionsYield
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
91749-17-6

trimethylsilyl <(dimethylamino)methyl>methylcarbamate

A

1,3,5-trimethyl-1,3,5-triazacyclohexane
108-74-7

1,3,5-trimethyl-1,3,5-triazacyclohexane

B

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

Conditions
ConditionsYield
at 20℃; for 360h; nitrogen atmosphere;A 90%
B n/a
bis-(dimethylamino)methane
51-80-9

bis-(dimethylamino)methane

bis(trimethylsilyl) 2-(2-furyl)ethylphosphonite
333364-16-2

bis(trimethylsilyl) 2-(2-furyl)ethylphosphonite

A

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

B

O-trimethylsilyl-[2-(2-furyl)ethyl](dimethylaminomethyl)phosphinate

O-trimethylsilyl-[2-(2-furyl)ethyl](dimethylaminomethyl)phosphinate

Conditions
ConditionsYield
With zinc(II) chloride at 130℃; for 1h;A n/a
B 83%
benzylthiotrimethylsilane
14629-67-5

benzylthiotrimethylsilane

N,N-dimethylphenylmethane sulfenamide
107427-35-0

N,N-dimethylphenylmethane sulfenamide

A

dibenzyl disulphide
150-60-7

dibenzyl disulphide

B

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

Conditions
ConditionsYield
at 80 - 110℃;A 72%
B 79%
trimethylsilyl iodide
16029-98-4

trimethylsilyl iodide

N,N-dimethyl acetamide
127-19-5

N,N-dimethyl acetamide

A

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

B

heptamethyldisilazane
920-68-3

heptamethyldisilazane

C

N-methyldiacetamide
1113-68-4

N-methyldiacetamide

D

methyl iodide
74-88-4

methyl iodide

Conditions
ConditionsYield
In dichloromethane at 35℃; for 5h;A 76%
B 1%
C 5%
D 3%
chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

dimethyl amine
124-40-3

dimethyl amine

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

Conditions
ConditionsYield
In methylbutane Ambient temperature;75%
In octane; acetonitrile at 20℃; for 5h; Solvent; Reflux;70%
bis-(dimethylamino)methane
51-80-9

bis-(dimethylamino)methane

bis(trimethylsilyl) [2-(2-furyl)-1-(trimethylsilyloxycarbonyl)ethyl]phosphonite
333361-87-8

bis(trimethylsilyl) [2-(2-furyl)-1-(trimethylsilyloxycarbonyl)ethyl]phosphonite

A

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

B

trimethylsilyl (dimethylaminomethyl)[2-(2-furyl)-1-(trimethylsiloxycarbonyl)ethyl]phosphinate
333361-89-0

trimethylsilyl (dimethylaminomethyl)[2-(2-furyl)-1-(trimethylsiloxycarbonyl)ethyl]phosphinate

Conditions
ConditionsYield
With zinc(II) chloride at 110 - 130℃; for 1.5h;A n/a
B 74%
N,N-dimethyl-P,P-dipropylphosphinous amide

N,N-dimethyl-P,P-dipropylphosphinous amide

A

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

B

dipropylphosphinous iodide
81373-58-2

dipropylphosphinous iodide

Conditions
ConditionsYield
With trimethylsilyl iodide In chlorobenzene at 110 - 132℃; for 8h;A n/a
B 63%
trimethylsilyl iodide
16029-98-4

trimethylsilyl iodide

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

A

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

B

N-formyl-N-methylformamide
18197-25-6

N-formyl-N-methylformamide

C

N-Methyl-N-(trimethylsilyl)-formamid
13889-02-6

N-Methyl-N-(trimethylsilyl)-formamid

D

formyl iodide
50398-22-6

formyl iodide

E

methyl iodide
74-88-4

methyl iodide

Conditions
ConditionsYield
In dichloromethane at 40℃; for 5h;A 61%
B 1%
C 11%
D 5%
E 11%
trimethylsilyl iodide
16029-98-4

trimethylsilyl iodide

Hexamethylphosphorous triamide
1608-26-0

Hexamethylphosphorous triamide

A

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

B

N,N,N',N'-tetramethylphosphorodiamidous iodide
20502-38-9

N,N,N',N'-tetramethylphosphorodiamidous iodide

Conditions
ConditionsYield
In dichloromethane Ambient temperature;A n/a
B 60%
bis-(dimethylamino)methane
51-80-9

bis-(dimethylamino)methane

C7H19PS4Si
153080-50-3

C7H19PS4Si

A

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

B

Tetrathiophosphoric acid dimethylaminomethyl ester diethyl ester

Tetrathiophosphoric acid dimethylaminomethyl ester diethyl ester

Conditions
ConditionsYield
at 100℃; for 1h;A 57%
B n/a
at 90 - 100℃;
methyl-bis(dimethylamino)phosphine
14937-39-4

methyl-bis(dimethylamino)phosphine

trimethylsilylazide
4648-54-8

trimethylsilylazide

A

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

B

N-trimethylsilyl-methylbis(dimethylaminophosphine) imine
82181-74-6

N-trimethylsilyl-methylbis(dimethylaminophosphine) imine

C

C11H33N5P2Si
82181-79-1

C11H33N5P2Si

Conditions
ConditionsYield
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
18135-05-2

N-(trimethylsilylmethyl)methylamine

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

Conditions
ConditionsYield
With n-butyllithium; hexane In tetrahydrofuran; benzene at 20.4 - 50.3℃; Kinetics;
trimethylsilyl bromide
2857-97-8

trimethylsilyl bromide

Hexamethylphosphorous triamide
1608-26-0

Hexamethylphosphorous triamide

A

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

B

Brom-bis-dimethylamino-phosphan
20502-36-7

Brom-bis-dimethylamino-phosphan

Conditions
ConditionsYield
Ambient temperature;
trimethylsilyl fluoride
420-56-4

trimethylsilyl fluoride

bis(dimethylamino)dimethylsilane
3768-58-9

bis(dimethylamino)dimethylsilane

Dimethyl-N-dimethylamino-fluor-silan
661-62-1

Dimethyl-N-dimethylamino-fluor-silan

A

dimethyldifluorosilane
353-66-2

dimethyldifluorosilane

B

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

Conditions
ConditionsYield
at 120℃; Equilibrium constant;
trimethylsilyl fluoride
420-56-4

trimethylsilyl fluoride

bis(dimethylamino)dimethylsilane
3768-58-9

bis(dimethylamino)dimethylsilane

A

dimethyldifluorosilane
353-66-2

dimethyldifluorosilane

B

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

C

Dimethyl-N-dimethylamino-fluor-silan
661-62-1

Dimethyl-N-dimethylamino-fluor-silan

Conditions
ConditionsYield
at 120℃; Equilibrium constant;
chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

Tetrakis(dimethylamino)methan
10524-51-3

Tetrakis(dimethylamino)methan

A

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

B

N,N,N',N',N'',N''-hexamethylguanidinium chloride
30388-20-6

N,N,N',N',N'',N''-hexamethylguanidinium chloride

Conditions
ConditionsYield
In toluene 0 deg C to r.t., overnight; Yield given;
chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

N,N-dimethylammonium chloride
506-59-2

N,N-dimethylammonium chloride

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

Conditions
ConditionsYield
With triethylamine; sodium iodide In acetonitrile for 0.5h; Ambient temperature; Yield given;
B2F4(N(CH3)2Si(CH3)3)
134620-31-8

B2F4(N(CH3)2Si(CH3)3)

A

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

B

diboron tetrafluoride
13965-73-6

diboron tetrafluoride

Conditions
ConditionsYield
In neat (no solvent) during heating of B2F4*NMe2SiMe3;
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

S-Trifluormethyldifluorosulfonium(IV) Hexafluoroarsenat
31842-51-0

S-Trifluormethyldifluorosulfonium(IV) Hexafluoroarsenat

Bis(dimethylamino)(trifluormethyl)sulfonium-hexafluoroarsenat
129813-16-7

Bis(dimethylamino)(trifluormethyl)sulfonium-hexafluoroarsenat

Conditions
ConditionsYield
-80 deg C -> RT;100%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

((E)-(2R,3S)-3-Hydroxy-2,4,6-trimethyl-hept-4-enyl)-triphenyl-phosphonium; iodide

((E)-(2R,3S)-3-Hydroxy-2,4,6-trimethyl-hept-4-enyl)-triphenyl-phosphonium; iodide

Triphenyl-((E)-(2R,3S)-2,4,6-trimethyl-3-trimethylsilanyloxy-hept-4-enyl)-phosphonium; iodide
136152-11-9

Triphenyl-((E)-(2R,3S)-2,4,6-trimethyl-3-trimethylsilanyloxy-hept-4-enyl)-phosphonium; iodide

Conditions
ConditionsYield
In dichloromethane100%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

chlorodimethylarsenium trifluoromethanesulfonate
141103-54-0

chlorodimethylarsenium trifluoromethanesulfonate

bis(dimethylamino)arsenium trifluoromethanesulfonate
141103-62-0

bis(dimethylamino)arsenium trifluoromethanesulfonate

Conditions
ConditionsYield
100%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

chlorodiethylarsenium trifluoromethanesulfonate
141103-56-2

chlorodiethylarsenium trifluoromethanesulfonate

diethylaminodimethylaminoarsenium trifluoromethanesulfonate
141103-64-2

diethylaminodimethylaminoarsenium trifluoromethanesulfonate

Conditions
ConditionsYield
100%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

Phenyl vinyl ketone
768-03-6

Phenyl vinyl ketone

Dimethyl-((Z)-3-phenyl-3-trimethylsilanyloxy-allyl)-amine

Dimethyl-((Z)-3-phenyl-3-trimethylsilanyloxy-allyl)-amine

Conditions
ConditionsYield
In diethyl ether for 15h; Ambient temperature;100%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

4-[4-(2-iodo-benzyl)-piperazin-1-yl]-cyclohexanone
749913-59-5

4-[4-(2-iodo-benzyl)-piperazin-1-yl]-cyclohexanone

{4-[4-(2-iodo-benzyl)-piperazin-1-yl]-cyclohex-1-enyl}-dimethyl-amine
749913-61-9

{4-[4-(2-iodo-benzyl)-piperazin-1-yl]-cyclohex-1-enyl}-dimethyl-amine

Conditions
ConditionsYield
With toluene-4-sulfonic acid100%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

4-[4-(2,5-difluoro-benzyl)-piperidin-1-yl]-cyclohexanone
749913-60-8

4-[4-(2,5-difluoro-benzyl)-piperidin-1-yl]-cyclohexanone

{4-[4-(2,5-difluoro-benzyl)-piperidin-1-yl]-cyclohex-1-enyl}-dimethyl-amine
749913-62-0

{4-[4-(2,5-difluoro-benzyl)-piperidin-1-yl]-cyclohex-1-enyl}-dimethyl-amine

Conditions
ConditionsYield
With toluene-4-sulfonic acid100%
{bis(trimethylsilyl)amino}-t-butylchloroborane
89487-06-9

{bis(trimethylsilyl)amino}-t-butylchloroborane

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

(tert-butyl)[bis(trimethylsilyl)amino](dimethylamino)borane
89487-12-7

(tert-butyl)[bis(trimethylsilyl)amino](dimethylamino)borane

Conditions
ConditionsYield
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
2083-91-2

N,N-Dimethyltrimethylsilylamine

S-(Perfluorethyl)thiazyldifluorid
111615-97-5

S-(Perfluorethyl)thiazyldifluorid

A

trimethylsilyl fluoride
420-56-4

trimethylsilyl fluoride

B

S-(Dimethylamino)-S-(perfluorethyl)thiazylfluorid
111615-99-7

S-(Dimethylamino)-S-(perfluorethyl)thiazylfluorid

Conditions
ConditionsYield
for 72h; -30 deg C to RT;A n/a
B 99%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

2,4,6-tris(dimethylamino)borazene
7360-02-3

2,4,6-tris(dimethylamino)borazene

Conditions
ConditionsYield
With 2,4,6-trichloroborazine In dichloromethane at 20℃;99%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

(R)-3-hydroxy-5-phenyl-pentanoic acid ethyl ester
182417-58-9

(R)-3-hydroxy-5-phenyl-pentanoic acid ethyl ester

(3R)-ethyl 5-phenyl-3-trimethylsilyloxy-pentanoate
465545-16-8

(3R)-ethyl 5-phenyl-3-trimethylsilyloxy-pentanoate

Conditions
ConditionsYield
at 20℃; for 16h;99%
for 16h;
bis(dimethylamino)chlorocarbenium bis(pentafluorethyl)phosphinate

bis(dimethylamino)chlorocarbenium bis(pentafluorethyl)phosphinate

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

hexamethylguanidinium bis(pentafluorethyl)phosphinate

hexamethylguanidinium bis(pentafluorethyl)phosphinate

Conditions
ConditionsYield
In chloroform at 20℃; for 1h;99%
B,B',B''-trichloroborazine
933-18-6

B,B',B''-trichloroborazine

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

2,4,6-tris(dimethylamino)borazene
7360-02-3

2,4,6-tris(dimethylamino)borazene

Conditions
ConditionsYield
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
2083-91-2

N,N-Dimethyltrimethylsilylamine

5-chloro-5H-dibenzo[a,d]cycloheptene
18506-04-2

5-chloro-5H-dibenzo[a,d]cycloheptene

(5-H-dibenzo[a,d]cyclohepten-5-yl)-dimethylamine
4889-29-6

(5-H-dibenzo[a,d]cyclohepten-5-yl)-dimethylamine

Conditions
ConditionsYield
In toluene Inert atmosphere;99%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

((C5(CH3)5)Fe(C5H4))2BBr
1233850-01-5

((C5(CH3)5)Fe(C5H4))2BBr

((C5(CH3)5)Fe(C5H4))2BN(CH3)2
1233850-03-7

((C5(CH3)5)Fe(C5H4))2BN(CH3)2

Conditions
ConditionsYield
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
16133-25-8

Pyridine-3-sulfonyl chloride

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

N,N-Dimethyl-3-pyridinsulfonsaeureamid

N,N-Dimethyl-3-pyridinsulfonsaeureamid

Conditions
ConditionsYield
In acetonitrile for 1h; Reflux; Inert atmosphere;99%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

dabsyl chloride
56512-49-3

dabsyl chloride

4-(4-(dimethylamino)diazenyl)-N,N-dimethylbenzenesulfonamide
72720-19-5

4-(4-(dimethylamino)diazenyl)-N,N-dimethylbenzenesulfonamide

Conditions
ConditionsYield
In acetonitrile for 1h; Reflux; Inert atmosphere;99%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

cyclopropanesulfonyl chloride
139631-62-2

cyclopropanesulfonyl chloride

N,N-dimethylcyclopropanesulfonamide

N,N-dimethylcyclopropanesulfonamide

Conditions
ConditionsYield
In acetonitrile for 1h; Reflux; Inert atmosphere;99%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

dansyl chloride
51278-33-2

dansyl chloride

5-(dimethylamino)-N,N-dimethylnaphthalene-2-sulfonamide
1467025-04-2

5-(dimethylamino)-N,N-dimethylnaphthalene-2-sulfonamide

Conditions
ConditionsYield
In acetonitrile for 1h; Reflux; Inert atmosphere;99%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

C50H38FeNO3S

C50H38FeNO3S

C45H37FeN2

C45H37FeN2

Conditions
ConditionsYield
With titanium tetrachloride In toluene at 55℃; for 17h;99%
6-methoxy-3-pyridinecarboxaldehyde
65873-72-5

6-methoxy-3-pyridinecarboxaldehyde

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

3-methoxy-1-iodobenzene
766-85-8

3-methoxy-1-iodobenzene

1-(3-methoxyphenyl)-1-(6-methoxypyridin-3-yl)-N,N-dimethylmethanamine

1-(3-methoxyphenyl)-1-(6-methoxypyridin-3-yl)-N,N-dimethylmethanamine

Conditions
ConditionsYield
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%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

2-chloro-1,4-dimethoxybenzene
2100-42-7

2-chloro-1,4-dimethoxybenzene

3,6-dimethoxy-2-(trimethylsilyl) N,N-dimethylbenzenamine

3,6-dimethoxy-2-(trimethylsilyl) N,N-dimethylbenzenamine

Conditions
ConditionsYield
With lithium di-1-admantylamide In diethyl ether; cyclohexane at 50℃; for 24h; Inert atmosphere;99%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

2,3,4,6-tetra-O-benzyl-D-galactopyranose
6386-24-9

2,3,4,6-tetra-O-benzyl-D-galactopyranose

trimethylsilyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranoside

trimethylsilyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranoside

Conditions
ConditionsYield
In dichloromethane at 20℃; for 0.5h; Inert atmosphere;99%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

C50H37FeNO3S

C50H37FeNO3S

C45H36FeN2

C45H36FeN2

Conditions
ConditionsYield
With titanium tetrachloride99%
pyridine-4-carbaldehyde
872-85-5

pyridine-4-carbaldehyde

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

A

Hexamethyldisiloxane
107-46-0

Hexamethyldisiloxane

B

(bis-dimethylamino methyl)-4 pyridine
122713-43-3

(bis-dimethylamino methyl)-4 pyridine

Conditions
ConditionsYield
With bromine; trimethylsilyl trifluoromethanesulfonate In tetrachloromethane for 48h; Ambient temperature;A n/a
B 98%
3-pyridinecarboxaldehyde
500-22-1

3-pyridinecarboxaldehyde

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

A

Hexamethyldisiloxane
107-46-0

Hexamethyldisiloxane

B

(bis-dimethylamino methyl)-3 pyridine
122713-46-6

(bis-dimethylamino methyl)-3 pyridine

Conditions
ConditionsYield
With bromine; trimethylsilyl trifluoromethanesulfonate In tetrachloromethane for 18h; Ambient temperature;A n/a
B 98%
furfural
98-01-1

furfural

N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

A

(bis-dimethylamino methyl)-2 furanne
33500-19-5

(bis-dimethylamino methyl)-2 furanne

B

Hexamethyldisiloxane
107-46-0

Hexamethyldisiloxane

Conditions
ConditionsYield
With bromine; trimethylsilyl trifluoromethanesulfonate In tetrachloromethane for 4h; Ambient temperature;A 98%
B n/a
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

methyl vinyl ketone
78-94-4

methyl vinyl ketone

Dimethyl-((Z)-3-trimethylsilanyloxy-but-2-enyl)-amine

Dimethyl-((Z)-3-trimethylsilanyloxy-but-2-enyl)-amine

Conditions
ConditionsYield
In diethyl ether for 15h; Ambient temperature;98%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

1-(Phenylsulfonyl)-1,2,3,4-tetrahydro-2-phenyl-4-quinolone
124857-02-9

1-(Phenylsulfonyl)-1,2,3,4-tetrahydro-2-phenyl-4-quinolone

1-Benzenesulfonyl-2-phenyl-4-trimethylsilanyloxy-1,2-dihydro-quinoline

1-Benzenesulfonyl-2-phenyl-4-trimethylsilanyloxy-1,2-dihydro-quinoline

Conditions
ConditionsYield
With toluene-4-sulfonic acid at 80℃; for 5h;98%
N,N-Dimethyltrimethylsilylamine
2083-91-2

N,N-Dimethyltrimethylsilylamine

1,3-bis(dibromoboryl)cymantrene
1010720-67-8

1,3-bis(dibromoboryl)cymantrene

Mn(CO)3C5H3(B(N(CH3)2)2)2
1148032-18-1

Mn(CO)3C5H3(B(N(CH3)2)2)2

Conditions
ConditionsYield
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%

N,N-Dimethyltrimethylsilylamine Chemical Properties

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.

N,N-Dimethyltrimethylsilylamine Uses

It can be used as raw material in organic synthesis.

N,N-Dimethyltrimethylsilylamine Safety Profile

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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