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 quantiti
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inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
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inquiryUnique advantages for Chlorotriethylsilane Cas 994-30-9 Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Colorles clear liquid Storage:N/A Package:25kg/drum,180kg/drum Applica
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inquiryhigh quality Appearance:White or off-white Solid Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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inquiryOur main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
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inquiryProduct Name: Chlorotriethylsilane Synonyms: CHLOROTRIETHYLSILANE;SILANE E3;TESCI;TESCL;chlorotriethyl-silan;CT2520;TRIETHYLCHLOROSILANE;TRIETHYLSILYL CHLORIDE CAS: 994-30-9 MF: C6H15ClSi MW: 150.72 EINECS: 213-
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inquiryProduct Description Product name Chlorotriethylsilane CAS 994-30-9 Assay 99% Appearance Colorless liqui
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inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturin
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
Cas:994-30-9
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inquiryProduct Name: Chlorotriethylsilane CAS: 994-30-9 MF: C6H15ClSi MW: 150.72 EINECS: 213-615-6 Appearance: Colorless Transparent Liqu
We can provide GMP validation service that complies with SFDA, FDA, WHO and EU EMPA.Excellent registration team could help us easlily to register our products in different countries.If you and your customer are interested in some products or need CMO
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inquiry1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; Appearance:Colorless Transparent Liquid Storage:Store in sealed contain
Cas:994-30-9
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inquirySynonyms: CHLOROTRIETHYLSILANE;SILANE E3;TESCI;TESCL;chlorotriethyl-silan;CT2520;TRIETHYLCHLOROSILANE;TRIETHYLSILYL CHLORIDE CAS: 994-30-9 MF: C6H15ClSi MW: 150.72 EINECS: 213-615-6 Product Categories: Other Reagents;Monochlorosilanes;Protecti
Cas:994-30-9
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inquiryOur company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At present,
Cas:994-30-9
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inquiryChlorotriethylsilane CAS:994-30-9 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 organic interm
Cas:994-30-9
Min.Order:1 Gram
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
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inquiryProduct Detail Minimum Order Qty. 10 Gram
Cas:994-30-9
Min.Order:10 Gram
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Type:Trading Company
inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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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
A 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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inquirylow price high quality high purity good sevice stock Appearance:white Storage:Preserve In Well-Closed, Light-Resistant and Tight Containers. Store In Cool & Dry Place Package:1g,5g,10g...1kg,5kg...more Application:Pharmaceutical intermediat
Cas:994-30-9
Min.Order:1 Gram
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inquiryConditions | Yield |
---|---|
With hexachloroethane; palladium dichloride at 20℃; for 1h; Cooling with ice; | 99.8% |
With hydrogenchloride; palladium on activated charcoal In hexane at 0℃; for 2h; | 87% |
With dichloromethane; eosin y at 40℃; Reagent/catalyst; Temperature; Flow reactor; Inert atmosphere; Irradiation; Green chemistry; | 86% |
triethylsilane
Phenyltrichlorosilane
A
triethylsilyl chloride
B
dichlorophenylsilane
Conditions | Yield |
---|---|
With tetra-n-butylphosphonium chloride at 100 - 120℃; for 3h; Inert atmosphere; | A 97.5% B 84.7% |
triethylsilyl phenylselenide
A
triethylsilyl chloride
B
diphenyl diselenide
Conditions | Yield |
---|---|
With chlorine In tetrachloromethane | A 96% B 96% |
phosgene
chloro-trimethyl-silane
Triethylsilanol
1,2-dichloro-ethane
triethylsilyl chloride
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide | 95% |
phosgene
chloro-trimethyl-silane
hexaethyl disiloxane
1,2-dichloro-ethane
triethylsilyl chloride
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide | 94.6% |
Conditions | Yield |
---|---|
With hydrogenchloride In water at 20℃; for 10h; | 90% |
With hydrogenchloride In hexane at 0℃; for 2h; | 72% |
Conditions | Yield |
---|---|
In neat (no solvent) (C2H5)3SiH and n-C6H13Cl in presence of AlCl3 at room temp.; vigorous react.;; | 88% |
With aluminium trichloride |
triethylsilane
vanadiumtetrachloride
A
triethylsilyl chloride
B
vanadium(III) chloride
Conditions | Yield |
---|---|
In neat (no solvent) in heating triethylsilane in 5 min;; | A 87% B n/a C n/a |
In neat (no solvent) in heating triethylsilane in 5 min;; | A 87% B n/a C n/a |
ethylpentachlorodisilane
triethylsilyl chloride
Conditions | Yield |
---|---|
With trimethylamine hydrochloride | 85% |
With (CH3)3N*HCl | 85% |
Conditions | Yield |
---|---|
With butyryl chloride; bis(acetylacetonate)nickel(II) at 90℃; for 2h; | A 83% B 68% |
chlorosulfonate de trimethylsilyle
2,4-Dimethyl-3-(triethylsiloxy)-2-penten
A
triethylsilyl chloride
B
2,4-Dimethyl-2-(trimethylsiloxysulfonyl)-3-pentanon
Conditions | Yield |
---|---|
In 1,2-dichloro-ethane for 3.5h; Ambient temperature; | A n/a B 81% |
triethylsilane
acetylene
A
triethylsilyl chloride
B
vinyltriethylsilane
Conditions | Yield |
---|---|
With aluminium trichloride at 40℃; for 2h; | A n/a B 80% |
triethylsilane
vanadium(V) oxychloride
C
triethylsilyl chloride
D
hydrogen
Conditions | Yield |
---|---|
A n/a B n/a C 80% D n/a | |
A n/a B n/a C 80% D n/a |
triethylsilane
bismuth(III) chloride
A
bismuth
B
triethylsilyl chloride
Conditions | Yield |
---|---|
byproducts: H2; heating dry powdered BiCl3 with triethyl silane under reflux;; | A n/a B 79% |
byproducts: H2; heating dry powdered BiCl3 with triethyl silane under reflux;; | A n/a B 79% |
Conditions | Yield |
---|---|
With HCl In hydrogenchloride (C2H5)3OH and an excess of concd. HCl at 0°C;; | 77% |
With HCl In hydrogenchloride (C2H5)3OH and an excess of concd. HCl at 0°C;; | 77% |
With hydrogenchloride; water | |
With hydrogenchloride In hexane at 0℃; for 2h; | 96 % Chromat. |
Triethyl(7,7,7-trichloroheptyl)silane
A
triethylsilyl chloride
B
hexaethyl disiloxane
C
7,7-Dichloro-1-heptene
D
(7,7-Dichloro-heptyl)-triethyl-silane
E
Triethyl-(3,7,7-trichloro-heptyl)-silane
Conditions | Yield |
---|---|
With iron pentacarbonyl; isopropyl alcohol at 140℃; for 3h; Mechanism; Product distribution; other metal carbonyl; other hydrogen donors, or PPh3; | A n/a B n/a C n/a D 77% E 10% |
triethylsilane
A
triethylsilyl chloride
B
hydrogen
C
ruthenium
Conditions | Yield |
---|---|
In not given react. with boiling (C2H5)3SiH after 12 min;; | A 74% B n/a C n/a |
In not given react. with boiling (C2H5)3SiH after 12 min;; | A 74% B n/a C n/a |
Conditions | Yield |
---|---|
With triethylsilane; bis(acetylacetonate)nickel(II) at 90℃; for 2h; | A 71% B 51% |
Conditions | Yield |
---|---|
With triethylsilane; bis(acetylacetonate)nickel(II) at 90℃; for 2h; | A 71% B 64% |
triethylsilane
A
triethylsilyl chloride
B
hexaethyl disiloxane
C
triethylsilyl acrylate
D
acrylic acid
Conditions | Yield |
---|---|
With iron(III)-acetylacetonate; acryloyl chloride at 20℃; for 0.333333h; Further byproducts given; | A 70% B 2% C 8% D 2% |
With iron(III)-acetylacetonate; acryloyl chloride at 20℃; for 0.333333h; Further byproducts given; | A 70% B 2% C 8% D 2% |
triethylsilane
acryloyl chloride
A
triethylsilyl chloride
B
hexaethyl disiloxane
C
triethylsilyl acrylate
D
acrylic acid
Conditions | Yield |
---|---|
With iron(III)-acetylacetonate at 20℃; for 0.333333h; Further byproducts given; | A 70% B 2% C 8% D 2% |
triethylsilane
acryloyl chloride
A
triethylsilyl chloride
B
hexaethyl disiloxane
C
triethylsilyl acrylate
D
acrylic acid
E
acrolein
Conditions | Yield |
---|---|
With iron(III)-acetylacetonate at 20℃; for 0.333333h; Product distribution; other reagents, other acyl chlorides; | A 70% B 2 % Chromat. C 8 % Chromat. D 2 % Chromat. E 8 % Chromat. |
acryloyl chloride
A
triethylsilyl chloride
B
hexaethyl disiloxane
C
triethylsilyl acrylate
D
acrylic acid
Conditions | Yield |
---|---|
With triethylsilane; iron(III)-acetylacetonate at 20℃; for 0.333333h; Further byproducts given; | A 70% B 2% C 8% D 2% |
triethylsilane
5,5,5-trichloro-1-pentene
A
triethylsilyl chloride
B
hexaethyl disiloxane
C
5,5,5-trichloropentyltriethylsilane
D
(E)-5,5,5-Trichloro-pent-2-ene
Conditions | Yield |
---|---|
With dihydrogen hexachloroplatinate; isopropyl alcohol at 20℃; for 48h; Further byproducts given; | A 0.7% B 2.3% C 67% D n/a |
Conditions | Yield |
---|---|
In hexane; toluene reaction in evacuated ampul; slow addn. of (Et3Si)2Hg (in toluene) to toluenic soln. Ni-compound (-40°C); left overnight; soln. becomes orange and pptn. of Hg; replacement of toluene by hexane; warming to -10°C;; elem. anal.; gas-liquid chromy.;; | A 61.7% B 37% C 20% |
triethylsilane
2-propynyl chloride
A
triethylsilyl chloride
B
triethylallylsilane
C
triethyl(propen-1-yl)silane
D
(3-chloro-1-propynyl)triethylsilane
Conditions | Yield |
---|---|
With dihydrogen hexachloroplatinate; iodine In tetrahydrofuran at 20℃; Further byproducts given; | A n/a B n/a C n/a D 61% |
triethylsilane
benzoyl chloride
A
triethylsilyl chloride
B
triethylsilyl benzoate
C
benzoic acid benzyl ester
D
benzaldehyde
E
benzoic acid
Conditions | Yield |
---|---|
iron(III)-acetylacetonate at 20℃; for 0.5h; Product distribution; other catalysts, other substrates; | A 60% B 16% C 9% D 13% E 3% |
triethylsilane
A
triethylsilyl chloride
B
(3-chloropropyl)triethylsilane
Conditions | Yield |
---|---|
With dihydrogen hexachloroplatinate; 3-chloroprop-1-ene at 50℃; for 6h; Title compound not separated from byproducts; | A 52% B 23% |
triethylsilane
3-chloroprop-1-ene
A
triethylsilyl chloride
B
(3-chloropropyl)triethylsilane
Conditions | Yield |
---|---|
With dihydrogen hexachloroplatinate at 50℃; for 6h; Product distribution; | A 52% B 23% |
With dihydrogen hexachloroplatinate at 50℃; for 6h; Title compound not separated from byproducts; | A 52% B 23% |
triethylsilyl chloride
2-methyl-but-3-yn-2-ol
2-methyl-2-<(triethylsilyl)oxy>-3-butyne
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane at 0℃; for 1h; | 100% |
10-deacetylbaccatin III
triethylsilyl chloride
7-triethylsilyl-10-deacetylbaccatin III
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide | 100% |
With pyridine Ambient temperature; | 98% |
In pyridine at 25℃; for 24h; | 97.7% |
triethylsilyl chloride
(3S,4S)-4-hydroxy-3-methyl-1-hexene
Triethyl-((S)-1-ethyl-2-methyl-but-3-enyloxy)-silane
Conditions | Yield |
---|---|
With 0,2,4-dichlorophenyl-0-methylisopropylamidothiophosphate; triethylamine In dichloromethane for 1h; Ambient temperature; | 100% |
triethylsilyl chloride
D-3,4,5,6-tetra-O-benzoyl-myo-inositol
D-3,4,5,6-tetra-O-benzoyl-1-O-triethylsilyl-myo-inositol
Conditions | Yield |
---|---|
With pyridine at 0℃; | 100% |
With pyridine for 2h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 0℃; for 1h; | 100% |
With triethylamine In N,N-dimethyl-formamide |
triethylsilyl chloride
(E)-(S)-6-[(1R,3R,3aR,3bS,6R,6aR,6bR)-3-(4-Methoxy-benzyloxy)-3a,6-dimethyl-decahydro-cyclobutadicyclopenten-1-yl]-2-methyl-hepta-3,6-diene-2,5-diol
(E)-(S)-6-[(1R,3R,3aR,3bS,6R,6aR,6bR)-3-(4-Methoxy-benzyloxy)-3a,6-dimethyl-decahydro-cyclobutadicyclopenten-1-yl]-2-methyl-5-triethylsilanyloxy-hepta-3,6-dien-2-ol
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane for 4h; Ambient temperature; | 100% |
With dmap; triethylamine In dichloromethane Yield given; |
triethylsilyl chloride
(4R,5S)-methyl 5-<(carbamoyl)oxy>-4-hydroxy-2-hexynoate
(4R,5S)-methyl 5-<(carbamoyl)oxy>-4-<(triethylsilyl)oxy>-2-hexynoate
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide for 1.5h; Ambient temperature; | 100% |
triethylsilyl chloride
2,6-Anhydro-4-O-benzyl-1-O-(tert-butyldiphenylsilyl)-3,7,8,9-tetradeoxy-D-altro-non-8-enitol
(2R,3S,4S,6S)-2-Allyl-4-benzyloxy-6-(tert-butyl-diphenyl-silanyloxymethyl)-3-triethylsilanyloxy-tetrahydro-pyran
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide at 25℃; | 100% |
With 1H-imidazole In N,N-dimethyl-formamide for 3.5h; Ambient temperature; | 100% |
triethylsilyl chloride
N-<(benzyloxy)carbonyl>-2-<(E)-5-(ethoxycarbonyl)-4-pentenyl>-2,3-dihydro-4-pyridone
N-<(benzyloxy)carbonyl>-2-(trans-5-(ethoxycarbonyl)-4-pentenyl)-4-(triethylsilyloxy)-1,2-dihydropyridine
Conditions | Yield |
---|---|
With sodium hexamethyldisilazane In tetrahydrofuran at -78℃; for 1h; | 100% |
triethylsilyl chloride
10-Deacetoxy-7-(triethylsilyl)baccatin III
7,13-Bis(triethylsilyl)-10-deoxybaccatin
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide Ambient temperature; | 100% |
triethylsilyl chloride
(2R,3S)-5-(benzyloxy)-3-hydroxy-N-methoxy-N,2-dimethylpentanamide
(2R,3S)-5-Benzyloxy-2-methyl-3-triethylsilanyloxy-pentanoic acid methoxy-methyl-amide
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide at 23℃; for 0.583333h; | 100% |
With 1H-imidazole In N,N-dimethyl-formamide at 23℃; Yield given; | |
With 1H-imidazole Etherification; |
triethylsilyl chloride
(2R,3R,4S,5S)-7-Benzyloxy-2,4-dimethyl-1-phenylsulfanyl-5-triethylsilanyloxy-heptan-3-ol
C34H58O3SSi2
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide at 23℃; for 2.5h; | 100% |
With 1H-imidazole In N,N-dimethyl-formamide at 23℃; |
triethylsilyl chloride
Conditions | Yield |
---|---|
With 1H-imidazole In dichloromethane for 6h; Heating; | 100% |
triethylsilyl chloride
oxiranyl-methanol
triethyl(oxiran-2-ylmethoxy)silane
Conditions | Yield |
---|---|
With 1H-imidazole; triethylamine In N,N-dimethyl-formamide silylation; | 100% |
With 1H-imidazole; dmap In dichloromethane at 20℃; for 1h; Inert atmosphere; | 100% |
With 1H-imidazole; dmap In dichloromethane at 0 - 20℃; for 3h; | 95% |
With dmap; triethylamine In dichloromethane at 0 - 20℃; | 84% |
With pyridine In diethyl ether for 0.75h; |
Conditions | Yield |
---|---|
In tetrahydrofuran | 100% |
triethylsilyl chloride
isopropyl (1S,2S,3R,5S)-5-(2-chloroethyl)-3-hydroxy-2-methylcyclopentane-1-carboxylate
isopropyl (1S,2S,3R,5S)-5-(2-chloroethyl)-3-triethylsiloxy-2-methylcyclopentane-1-carboxylate
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide for 1h; Ambient temperature; | 100% |
triethylsilyl chloride
Conditions | Yield |
---|---|
With triethylamine; lithium diisopropyl amide In tetrahydrofuran; hexane 1.) -78 deg C, 30 min, 2.) -78 deg C, 1 h; -78 deg C to r.t., 40 min; | 100% |
triethylsilyl chloride
Conditions | Yield |
---|---|
With pyridine at 35℃; | 100% |
triethylsilyl chloride
2,2-Dimethyl-propionic acid (3R,4R,5S,6S)-5-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-4,6-dimethyl-7-phenylsulfanyl-heptyl ester
2,2-Dimethyl-propionic acid (3R,4R,5S,6S)-5-(tert-butyl-dimethyl-silanyloxy)-4,6-dimethyl-7-phenylsulfanyl-3-triethylsilanyloxy-heptyl ester
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide at 23℃; for 1.4h; | 100% |
With 1H-imidazole In N,N-dimethyl-formamide |
triethylsilyl chloride
(3aR,4S,5S,6R.7aS)-5,6-epoxy-3a,4,5,6,7,7a-hexahydro-4-hydroxy-6-methyl-2(3H)-benzofuranone
(1aR,2aS,5aS,6S,6aS)-2,2a,5,5a,6,6a-hexahydro-1a-methyl-6-<(triethylsilyl)oxy>oxirenobenzofuran-4(1aH)-one
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane for 0.5h; Ambient temperature; | 100% |
With dmap; triethylamine In dichloromethane for 3.5h; Ambient temperature; | 75% |
triethylsilyl chloride
(S)-oxiranemethanol
(R)-(triethylsilyl)glycidyl ether
Conditions | Yield |
---|---|
With 1H-imidazole; dmap In dichloromethane at 0 - 20℃; for 2h; | 100% |
With 1H-imidazole In dichloromethane at 0 - 20℃; for 1h; Inert atmosphere; | 94% |
With dmap; triethylamine at -30℃; |
triethylsilyl chloride
1D-1,2-O-cyclohexylidene-6-O-(4-oxopentanoyl)-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-myo-inositol
1D-1,2-O-cyclohexylidene-6-O-levulinoyl-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol
Conditions | Yield |
---|---|
100% | |
With dmap; triethylamine In dichloromethane Ambient temperature; Yield given; |
(S)-Ethyl lactate
triethylsilyl chloride
α-(triethylsiloxy)propanoic acid ethyl ester
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; | 100% |
With 1H-imidazole In dichloromethane at 20℃; for 16h; Schlenk technique; Inert atmosphere; | 85% |
With 1H-imidazole In N,N-dimethyl-formamide for 3h; Ambient temperature; |
triethylsilyl chloride
(7R,8S,8aS)-8-((E)-But-1-enyl)-7-hydroxy-hexahydro-indolizin-3-one
(7R,8S,8aS)-8-((E)-But-1-enyl)-7-triethylsilanyloxy-hexahydro-indolizin-3-one
Conditions | Yield |
---|---|
In pyridine for 14h; Ambient temperature; | 100% |
With pyridine Yield given; |
triethylsilyl chloride
(-)-(1R,2S)-2-phenyl-1-cyclohexyl hydroxyacetate
Triethylsilanyloxy-acetic acid (1R,2S)-2-phenyl-cyclohexyl ester
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; | 100% |
triethylsilyl chloride
2,2-Dimethyl-propionic acid (4S,5S)-5-[(2R,3R,4R,5R)-3-hydroxy-4-methoxymethoxy-5-(2-trityloxy-ethyl)-tetrahydro-furan-2-yl]-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester
2,2-Dimethyl-propionic acid (4S,5S)-5-[(2S,3R,4S,5R)-4-methoxymethoxy-3-triethylsilanyloxy-5-(2-trityloxy-ethyl)-tetrahydro-furan-2-yl]-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester
Conditions | Yield |
---|---|
With 1H-imidazole; dmap In N,N-dimethyl-formamide at 40℃; for 15h; | 100% |
triethylsilyl chloride
(2R,4S,8S,10R)-4-(tert-Butyl-diphenyl-silanyloxy)-8-hydroxy-2,10-bis-(4-methoxy-benzyloxy)-1-(2-trimethylsilanyl-ethoxymethoxy)-tridec-12-en-6-one
(2R,4S,8S,10R)-4-(tert-Butyl-diphenyl-silanyloxy)-2,10-bis-(4-methoxy-benzyloxy)-8-triethylsilanyloxy-1-(2-trimethylsilanyl-ethoxymethoxy)-tridec-12-en-6-one
Conditions | Yield |
---|---|
With 1H-imidazole In dichloromethane; N,N-dimethyl-formamide for 1h; | 100% |
triethylsilyl chloride
taxinine A
Acetic acid (1R,2R,3R,5S,8R,9R,10R)-2,10-diacetoxy-8,12,15,15-tetramethyl-4-methylene-13-oxo-5-triethylsilanyloxy-tricyclo[9.3.1.03,8]pentadec-11-en-9-yl ester
Conditions | Yield |
---|---|
With 1H-imidazole In dichloromethane for 4h; Ambient temperature; | 100% |
With 1H-imidazole In dichloromethane for 3h; Ambient temperature; | 98% |
triethylsilyl chloride
2-ethyl-2-(2-iodophenyl)butan-1-ol
triethyl-[2-ethyl-2-(2-iodophenyl)butoxy]silane
Conditions | Yield |
---|---|
With pyridine for 0.5h; Ambient temperature; | 100% |
triethylsilyl chloride
(1-Ethyl-8-iodo-1,2,3,4-tetrahydro-naphthalen-1-yl)-methanol
Triethyl-(1-ethyl-8-iodo-1,2,3,4-tetrahydro-naphthalen-1-ylmethoxy)-silane
Conditions | Yield |
---|---|
With pyridine for 0.5h; Ambient temperature; | 100% |
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