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Cas:13822-56-5
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inquiryItems Standard Result Appearance Colorless clear liquid Complies Assay 97%min 9
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inquiryChemical Name :3-aminopropyltrimethoxysilane Molecular Formula :C6H17NO3Si Molecular structure: CAS NO.: 13822-56-5 Foreign Company's Trademark: A-1110 Appearance:Colorless Transparent liquid. Storage:in cool, dry place Packa
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inquiryTIANFUCHEM--13822-56-5--3-(Trimethoxysilyl)-1-propanamine in stock Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had established stable busi
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inquiryProduct Description Product website: http://www.finerchem.com Product Name 3-Aminopropyltrimethoxysilane CAS No. 13822-56-5
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inquiryProduct Name 3-Aminopropyltrimethoxysilane CAS NO. 13822-56-5 Molecular Formula C36H17NOSi Molecular Weight 179.29 Appearance colorless tran
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inquiryProduct Name: 3-Aminopropyltrimethoxysilane CAS: 13822-56-5 MF: C6H17NO3Si MW: 179.29 EINECS: 237-511-5 Mol File: 13822-56-5.mol 3-Aminopropyltrimethoxysilane Structure 3-Aminopropyltrimethoxysilane Chemical Properties Melting poi
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inquiry3-Aminopropyltrimethoxysilane CAS:13822-56-5 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality org
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inquiryA substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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inquiry13822-56-5 Chemical name:3-Aminopropyltrimethoxysilane Synonyms:1-Propanamine,3-(trimethoxysilyl)-; Formula:H2N(CH2)3Si(OCH3)3 Description:Colorless Transparent liquid. Superiority 1.Powerful R & D team 2.The ability of quanti
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inquirytrimethoxysilane
Triethoxysilane
A
beta-amminopropyl trimethoxy silane
B
3-(trimethoxysilyl)propan-1-amine
Conditions | Yield |
---|---|
A 70% B n/a |
trimethoxysilane
Triethoxysilane
A
beta-aminopropyl triethoxy silane
B
3-(trimethoxysilyl)propan-1-amine
Conditions | Yield |
---|---|
A 62% B n/a | |
A 62% B n/a |
3-Chloropropyltrimethoxysilan
3-(trimethoxysilyl)propan-1-amine
Conditions | Yield |
---|---|
With ammonia |
methanol
C9H23NO4Si
A
2-ethoxy-ethanol
B
3-(trimethoxysilyl)propan-1-amine
Conditions | Yield |
---|---|
at 20℃; Kinetics; Equilibrium constant; |
trimethoxysilane
1-amino-2-propene
A
beta-aminoisopropyltrimethoxysilane
B
3-(trimethoxysilyl)propan-1-amine
Conditions | Yield |
---|---|
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex at 80℃; for 20h; Catalytic behavior; Schlenk technique; Inert atmosphere; Overall yield = 94.3 %Spectr.; regioselective reaction; |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 12h; | 100% |
1-Bromonaphthalene
3-(trimethoxysilyl)propan-1-amine
Methyl 1-naphthylphosphinate
Conditions | Yield |
---|---|
With anilinium hypophosphorous salt; 1,3-bis-(diphenylphosphino)propane; palladium diacetate In acetonitrile Heating; | 100% |
5-isothiocyanato-1,10-phenanthroline
3-(trimethoxysilyl)propan-1-amine
N-(1,10-phenanthrolin-5-yl)-N'-(3-trimethoxysilylpropyl)thiourea
Conditions | Yield |
---|---|
In dichloromethane; pentane at 0℃; for 0.166667h; | 100% |
3-(trimethoxysilyl)propan-1-amine
1-[(2-oxazepan-1-yl)carbonyl]azepan-2-one
A
caprolactam
Conditions | Yield |
---|---|
In toluene at 75℃; for 3h; | A n/a B 100% |
acrylic acid-2-[N-methyl][(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)-1-sulfonylamino]-ethyl ester
3-(trimethoxysilyl)propan-1-amine
Conditions | Yield |
---|---|
at 70℃; for 5h; | 100% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 1h; | 99.1% |
Conditions | Yield |
---|---|
With lithium hydride In tetrahydrofuran for 2h; Heating; | 99% |
Conditions | Yield |
---|---|
With potassium hydride In tetrahydrofuran for 2h; Heating; | 99% |
3-(trimethoxysilyl)propan-1-amine
carbonic acid dimethyl ester
N-(3-trimethoxysilylpropyl) O-methyl carbamate
Conditions | Yield |
---|---|
With sodium methylate In methanol at 55 - 80℃; for 3.5h; Temperature; Time; | 99% |
With sodium methylate In methanol at 55 - 80℃; for 4h; Large scale; | 99% |
With 8Na(1+)*12C4H10NO(1-)*2HO(1-)*2Nd(3+) In neat (no solvent) at 80℃; for 12h; Inert atmosphere; Schlenk technique; Green chemistry; | 90% |
succinic acid anhydride
3-(trimethoxysilyl)propan-1-amine
4-oxo-4-[3-(trimethoxysilyl)propylamino]butanoic acid
Conditions | Yield |
---|---|
In tetrahydrofuran at -5 - 5℃; for 6h; Inert atmosphere; | 99% |
Inert atmosphere; | 98% |
In tetrahydrofuran at 20℃; for 18h; Inert atmosphere; |
Pyridine-2,3-dicarboxylic anhydride
3-(trimethoxysilyl)propan-1-amine
Conditions | Yield |
---|---|
In tetrahydrofuran at -5 - 5℃; for 5h; Inert atmosphere; | 99% |
3-(trimethoxysilyl)propan-1-amine
trimellitic Anhydride
C15H21NO8Si
Conditions | Yield |
---|---|
In tetrahydrofuran at -5 - 5℃; for 6h; Inert atmosphere; | 99% |
3-(trimethoxysilyl)propan-1-amine
urea
3-(trimethoxysilyl)propyl isocyanate
Conditions | Yield |
---|---|
Stage #1: 3-(trimethoxysilyl)propan-1-amine; urea With Trimethyl orthoacetate In dimethyl sulfoxide at 90 - 95℃; for 9h; Stage #2: With sulfuric acid; copper(II) oxide In dimethyl sulfoxide at 75 - 80℃; for 4.5h; pH=6.5; Concentration; Temperature; pH-value; | 98.2% |
Stage #1: 3-(trimethoxysilyl)propan-1-amine; urea In methanol at 180℃; under 8250.83 - 10501.1 Torr; for 12.5h; Stage #2: With tin(ll) chloride at 195℃; under 56.2556 Torr; | 92% |
ethanol
3-(trimethoxysilyl)propan-1-amine
sodium hydroxide
B
sodium chloride
Conditions | Yield |
---|---|
In methanol; water Si-compd. dissoln. in MeOH, aq. soln. of NaOH addn., refluxing (1 h), soln. of Cu-compd. in MeOH addn., refluxing (30 min), MeOH distillation off with simultaneous addn. of EtOH; NaCl filtration off, solvent removing; elem. anal.; | A 93% B 98% |
3-(trimethoxysilyl)propan-1-amine
Conditions | Yield |
---|---|
With ammonium hydrogen difluoride In water at 20℃; | 98% |
[2-(acryloyloxy)ethyl]trimethylammonium bis-(trifluoromethane)sulfonimide
3-(trimethoxysilyl)propan-1-amine
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 5h; | 97.6% |
Conditions | Yield |
---|---|
In toluene Heating; | 97% |
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran at 0 - 65℃; Product distribution; Further Variations:; Reagents; Solvents; Temperatures; | 97% |
Conditions | Yield |
---|---|
In dichloromethane at 5℃; Inert atmosphere; | 97% |
In dichloromethane at 5 - 20℃; Inert atmosphere; | 97% |
3-(trimethoxysilyl)propan-1-amine
trans-4-(4-Heptylcyclohexyl)benzoesaeurechlorid
Conditions | Yield |
---|---|
With triethylamine In toluene at 5 - 20℃; for 17.5h; | 97% |
3-(trimethoxysilyl)propan-1-amine
trifluoroacetic acid
Conditions | Yield |
---|---|
In water at 20℃; for 2h; Inert atmosphere; Schlenk technique; | 97% |
3-(trimethoxysilyl)propan-1-amine
bis(trifluoromethanesulfonyl)amide
Conditions | Yield |
---|---|
In water; dimethyl sulfoxide at 25 - 100℃; for 19h; | 97% |
2-dimethylaminoethyl isothiocyanate
3-(trimethoxysilyl)propan-1-amine
1-(2-Dimethylamino-ethyl)-3-(3-trimethoxysilyl-propyl)-thiourea
Conditions | Yield |
---|---|
In 1,4-dioxane at 20℃; for 20h; Heating / reflux; | 96.6% |
carbon disulfide
3-(trimethoxysilyl)propan-1-amine
Conditions | Yield |
---|---|
Stage #1: carbon disulfide; 3-(trimethoxysilyl)propan-1-amine In tetrahydrofuran at 0 - 5℃; for 3h; Addition; Stage #2: With CYANAMID; triethylamine In tetrahydrofuran at 40℃; for 3h; Elimination; | 96% |
3-(trimethoxysilyl)propan-1-amine
3-hydroxy-1,2,3-benzotriazin-4(3H)-one ester of di-isopropylthio-acetic acid
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 4h; | 96% |
3-(trimethoxysilyl)propan-1-amine
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 1h; Inert atmosphere; Schlenk technique; | 96% |
2-bromoisobutyric acid bromide
3-(trimethoxysilyl)propan-1-amine
Conditions | Yield |
---|---|
With triethylamine In dichloromethane for 14h; | 95.1% |
With triethylamine In dichloromethane for 2h; Cooling with ice; Inert atmosphere; |
3-(trimethoxysilyl)propan-1-amine
p-(iodophenyl)carboxaldehyde
Conditions | Yield |
---|---|
In methanol for 20h; Heating; | 95% |
3-(trimethoxysilyl)propan-1-amine
phenyl isothiocyanate
N-phenyl-N'-[3-(trimethoxysilyl)propyl]thiourea
Conditions | Yield |
---|---|
With triethylamine In dichloromethane for 24h; | 95% |
With triethylamine In chloroform at 50℃; |
3-(trimethoxysilyl)propan-1-amine
butyl isothiocyanate
N-butyl-N'-[3-(trimethoxysilyl)propyl]thiourea
Conditions | Yield |
---|---|
With triethylamine In dichloromethane for 24h; | 95% |
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