Dayangchem's R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. DayangChem can provide different quantities
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inquiryName: N,N-Dimethyltrimethylsilylamine Synonyms: pentamethylsilylamine CAS: 2083-91-2 MF: C7H21NSi2 Appearance:Colorless clear liquid Storage:Preserve in well-closed, light-resistant and airtight containers. Package:25kg/drum Application:Syntheses
Cas:2083-91-2
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Min.Order:1 Gram
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inquiryCompany Introduction 1. Established in 2005, with two independent business divisions: Fine chemicals division; Pharmaceutical division. 2. Main product: Optical brightener Textile auxiliary Dye stuff Pigments
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Min.Order:1 Gram
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
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inquiryProduct name: N,N-Dimethyltrimethylsilylamine CAS No.:2083-91-2 Molecule Formula:C7H21NSi2 Molecule Weight:175.42 Purity: 99.0% Package: 25kg/drum Description:White powder Manufacture Standards:Enterprise Standard TESTING ITEMS
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Min.Order:1 Kilogram
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inquiryZhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed
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Min.Order:1 Kilogram
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inquiryStock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
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inquiryJinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
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Min.Order:100 Gram
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inquiryAcmec is a leading manufacturer and supplier of biochemical reagents and life science products. We have over 40,000 items in stock (real-time inventory) and offer discounted prices to registered members of the online store ( www.acmec.com.cn ) Appea
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inquiryhigh quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
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inquirygood quality, competitive price, thoughtful after sale serviceAppearance:White to Off-White Solid Storage:Keep it in dry,shady and cool place Package:as your requirement Application:Pharma;Industry;Agricultural;chemical reaserch Transportation:by Sea
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inquiryWe are committed to providing our customers with the best products and services at the most competitive prices.Appearance:light yellow liquid Storage:Room temperature with sealed well Package:according to the clients requirement Application:Use as pr
N,N-Dimethyltrimethylsilylamine cas 2083-91-2Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
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inquiryHangzhou ZeErRui Chemical Co., Ltd. located in Lingang industrial areas, our plant covers an area of 6000 square meters.ZeErRui dedicated to the development, production and marketing of chemicals. We have earned ourselves a good reputation at home an
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inquiryStock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
home-produced Application:medicine
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inquiryKnown for its best quality and competitve price, this chemicals we offered is widely appreciated by our customers.Appearance:White powder Storage:keep sealed and keep from direct light Package:According client's requirements Application:pharmaceutica
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inquiryfactory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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% |
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