DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:941-55-9
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inquiryCAS: 941-55-9 MF: C7H7N3O2S MW: 197.21 EINECS: 213-381-5 Product Categories: Mol File: 941-55-9.mol Tosyl azide Structure Tosyl azide Chemical Properties Melting point 22 °C density ~0.90 g/mL at 20 °C refractive
Our 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 prese
Cas:941-55-9
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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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Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
J&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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Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Product name: P-Toluenesulfonyl Azide CAS No.: 941-55-9 Molecule Formula:C7H8N3O2S Molecule Weight:198.22 Purity: 99.0% Package: 200kg/drum Description:Colorless or pale yellow liquid Manufacture Standards:Enterprise Standard TES
Cas:941-55-9
Min.Order:1 Kilogram
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inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
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factory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
Shandong Mopai Biotechnology Co., LTD is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemicals. W
1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
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SAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in custom synthe
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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
Shanghai Lonwin Chemical company is a subsidiary of Lonwin Industry Group Limited, was established in 2011 and is headquartered in Shanghai, adjacent to China National Convention and Exhibition Center and Hongqiao transportation hub.Lonwinchem is
Cas:941-55-9
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inquiryConditions | Yield |
---|---|
With sodium azide In water; isopropyl alcohol at 20℃; for 1h; | 100% |
With sodium azide In water; acetone at 0 - 23℃; for 17h; Inert atmosphere; | 100% |
With sodium azide In water; acetone at 0 - 23℃; for 17h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With trimethylsilylazide; 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 50℃; for 1.5h; | 98% |
Conditions | Yield |
---|---|
Stage #1: toluene-4-sulfonic acid With trichloroisocyanuric acid; triphenylphosphine In tetrahydrofuran at 0 - 5℃; for 0.25h; Stage #2: With sodium azide In tetrahydrofuran at 5 - 20℃; for 0.0166667h; Solvent; | 97% |
With sodium azide; trichloroacetonitrile; triphenylphosphine In acetonitrile at 20℃; for 3h; | 95% |
Stage #1: toluene-4-sulfonic acid With 1-ethyl-3-methylimidazolium tetrafluoroborate; triethylamine at 0℃; for 0.0833333h; Stage #2: With sodium azide; bis(trichloromethyl) carbonate at 0 - 25℃; for 1.5h; | 89% |
With sodium azide; trichloroisocyanuric acid; triphenylphosphine In tetrahydrofuran at 20℃; |
Conditions | Yield |
---|---|
With SHNC In water for 0.75h; Ambient temperature; | 96% |
With dinitrogen tetraoxide In tetrachloromethane; acetonitrile at -20℃; for 0.166667h; Product distribution; other t; | 95% |
With dinitrogen tetraoxide In tetrachloromethane; acetonitrile at -20℃; for 0.166667h; | 95% |
Conditions | Yield |
---|---|
With 3-azidosulfonyl-3H-imidazole-1-ium hydrogen sulfate; potassium carbonate In water; isopropyl alcohol at 20℃; for 18h; Solvent; Concentration; | 90% |
With sodium azide In water; acetone at 20℃; for 2h; | 87% |
With copper(ll) sulfate pentahydrate; sodium hydrogencarbonate; perfluorobutanesulfonyl azide In methanol; diethyl ether; water at 20℃; for 6h; | 81% |
A
4-toluenesulfonyl azide
B
(η(5)-cyclopentadienyl)[1,2-bis(methoxycarbonyl)ethenethiolato-κS]cobalt(III)
Conditions | Yield |
---|---|
In neat (no solvent) 177-178°C; | A 43% B 88% |
Conditions | Yield |
---|---|
With sodium azide; water In acetonitrile for 4h; Heating; | 88% |
7-Methoxy-1-<(4-methylphenyl)sulfonyl>-3,4-dihydropyrrolo<4,3,2-de>quinolin-8(1H)-one
A
4-toluenesulfonyl azide
B
7-Methoxy-2,4-dihydropyrrolo<4,3,2-de>quinolin-8(1H)-one
Conditions | Yield |
---|---|
With sodium azide; N,N-dimethyl-formamide at 25℃; for 4h; | A n/a B 84% |
toluene-4-sulfonic acid 4-methyl-5-oxo-2,5-dihydro-furan-3-yl ester
A
4-toluenesulfonyl azide
B
4-hydroxy-3-methyl-5H-furan-2-one
Conditions | Yield |
---|---|
With sodium azide In methanol at 20℃; Substitution; | A n/a B n/a C 20% |
toluene-4-sulfonic acid 4-(3,4-dimethoxy-phenyl)-5-oxo-2,5-dihydro-furan-3-yl ester
A
4-toluenesulfonyl azide
B
3-(3,4-dimethoxyphenyl)-4-hydroxy-5H-furan-2-one
Conditions | Yield |
---|---|
With sodium azide In methanol at 20℃; Substitution; | A n/a B n/a C 20% |
N-tosyl dimethylketenimine
A
4-toluenesulfonyl azide
B
Isobutyronitrile
C
N-[1-Amino-2-methyl-prop-2-en-(Z)-ylidene]-4-methyl-benzenesulfonamide
D
C22H28N2O5S2
Conditions | Yield |
---|---|
With tris-(2-chloro-ethyl)-amine In diethyl ether Product distribution; | A n/a B n/a C 14% D 3% |
With tris-(2-chloro-ethyl)-amine In diethyl ether | A n/a B n/a C 14% D 3% |
N-[1-Chloro-2-methyl-prop-(Z)-ylidene]-4-methyl-benzenesulfonamide
A
4-toluenesulfonyl azide
B
Isobutyronitrile
Conditions | Yield |
---|---|
With lithium azide In diethyl ether; N,N-dimethyl-formamide at -20 - 20℃; Product distribution; |
4-toluenesulfonyl azide
Conditions | Yield |
---|---|
With acetic acid; sodium nitrite |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 70 percent / K2CO3 / acetone / 20 °C 2: NaN3 / methanol / 20 °C View Scheme |
4-(4-toluenesulfonyloxy)coumarin
4-toluenesulfonyl azide
Conditions | Yield |
---|---|
With sodium azide In dimethyl sulfoxide for 1h; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: N-chloro-succinimide; tetrabutyl-ammonium chloride; water / acetonitrile / 0 °C 2: sodium azide / acetonitrile / 0.75 h / 20 °C View Scheme | |
Multi-step reaction with 2 steps 1: tetrabutyl-ammonium chloride; water; N-chloro-4-methylbenzenesulfonamide / acetonitrile / 0.5 h / 0 °C 2: sodium azide / acetonitrile / 0.75 h / 0 - 20 °C View Scheme |
2,4-Dinitrophenol
p-toluenesulfonyl chloride
A
4-toluenesulfonyl azide
B
1-azido-2,4-dinitrobenzene
C
toluene-4-sulfonic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: triethylamine / diethyl ether 2: sodium azide / dimethyl sulfoxide; water; acetonitrile / 25 °C View Scheme |
2,4-dinitrophenyl 4-methylbenzenesulfonate
A
4-toluenesulfonyl azide
B
2,4-Dinitrophenol
C
1-azido-2,4-dinitrobenzene
D
toluene-4-sulfonic acid
Conditions | Yield |
---|---|
With sodium azide In water; dimethyl sulfoxide; acetonitrile at 25℃; Kinetics; Mechanism; regioselective reaction; |
Conditions | Yield |
---|---|
With C36H55N2*Pd(2+)*C7H7NO2S(2-); hydrogen In benzene-d6 at 75℃; for 12h; Temperature; Time; | 100% |
With iron(III) oxide; hydrazine hydrate In water at 120℃; for 1.5h; Inert atmosphere; | 99% |
With D-glucose; potassium hydroxide In water at 85℃; for 0.0833333h; Green chemistry; chemoselective reaction; | 99% |
4-toluenesulfonyl azide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 18℃; | 100% |
4-toluenesulfonyl azide
Conditions | Yield |
---|---|
In dichloromethane-d2 at -78℃; for 144h; | 100% |
1,4-Dihydro-1,4-dimethyl-5-(2,2-dimethylpropyliden)-5H-tetrazol
4-toluenesulfonyl azide
Conditions | Yield |
---|---|
In toluene at 20℃; for 1h; | 100% |
4-toluenesulfonyl azide
thiolane-2,5-dione
benzylamine
N-(4-methylphenylsulfonyl)-N'-(phenylmethyl)-butanediamide
Conditions | Yield |
---|---|
Stage #1: thiolane-2,5-dione; benzylamine In methanol for 0.5h; Stage #2: 4-toluenesulfonyl azide With 2,6-dimethylpyridine In methanol for 0.5h; Further stages.; | 100% |
methyl 5-acetamido-2,6-anhydro-3,5-dideoxy-8,9-O-isopropylidene-4-O-(2-propynyl)-D-glycero-D-galacto-non-2-enonate
4-toluenesulfonyl azide
diisopropylamine
methyl 5-acetamido-2,6-anhydro-3,5-dideoxy-8,9-O-isopropylidene-4-O-[3-(diisopropylamino)-3-(4-methylbenzenesulfonylimino)propoxy]-D-glycero-D-galacto-non-2-enonate
Conditions | Yield |
---|---|
With copper(l) iodide In dichloromethane at 20℃; for 1h; Inert atmosphere; | 100% |
4-toluenesulfonyl azide
Conditions | Yield |
---|---|
With triethylamine In acetonitrile at 20℃; for 16h; | 100% |
4-toluenesulfonyl azide
Conditions | Yield |
---|---|
With copper(I) thiophene-2-carboxylate In dichloromethane at 20℃; for 3h; | 99.2% |
4-toluenesulfonyl azide
ethyl 5-(2,2-dimethyl-1,1-diphenyl-1-silapropoxy)-3-oxohept-6-enoate
ethyl 5-(2,2-dimethyl-1,1-diphenyl-1-silapropoxy)-2-diazo-3-oxohept-6-enoate
Conditions | Yield |
---|---|
With triethylamine In acetonitrile Diazotization; | 99% |
Conditions | Yield |
---|---|
Stage #1: chloro-diphenylphosphine With sodium In tetrahydrofuran for 18h; Heating; Stage #2: 4-toluenesulfonyl azide In tetrahydrofuran; acetone at 20℃; for 48h; Staudinger reaction; | 99% |
Conditions | Yield |
---|---|
With 4 A molecular sieve; chiral (CO)Ru(II)(salen) In dichloromethane at 20℃; for 24h; | 99% |
4-toluenesulfonyl azide
methyl-phenyl-thioether
S-methyl-S-phenyl-N-(p-tolylsulfonyl)sulfimide
Conditions | Yield |
---|---|
With MS 4 Angstroem; bis(salicylaldehyde)ethylenediiminatocarbonylruthenium(II) In dichloromethane at 20℃; | 99% |
With (5,10,15,20-tetrakis(pentafluorophenyl)porphyrinato)iron(III) chloride In 1,2-dichloro-ethane for 24h; Molecular sieve; Inert atmosphere; Reflux; | 94% |
With D-glucose; cytochrome P-I263F A328V variant; NADPH In aq. phosphate buffer; dimethyl sulfoxide at 20℃; for 20h; pH=8; Reagent/catalyst; Enzymatic reaction; | 63% |
4-toluenesulfonyl azide
4-trifluoromethylphenylacetylene
diisopropylamine
Conditions | Yield |
---|---|
With copper(l) iodide In tetrahydrofuran at 20℃; for 1h; | 99% |
4-toluenesulfonyl azide
phenylacetylene
1-(4-methylbenzensulfonyl)-4-phenyl-1H-1,2,3-triazole
Conditions | Yield |
---|---|
With copper(I) thiophene-2-carboxylate; benzoic acid In benzene at 60℃; for 0.05h; Flow reactor; | 99% |
With (N,N’-bis-{2,6-(di-iso-propyl)phenyl}imidazole-2-ylidene)tri-tert-butylphosphinetetrafluoroborate copper (I) In toluene at 20℃; for 15h; Reagent/catalyst; Solvent; Temperature; | 97% |
With copper(II) acetate monohydrate; 2-amino-phenol In acetonitrile at 20℃; for 0.333333h; regioselective reaction; | 95% |
Conditions | Yield |
---|---|
With copper(l) iodide; water; triethylamine at 25℃; for 1h; | 99% |
4-toluenesulfonyl azide
2-ethynyl-1-nitrobenzene
1-(4-methylbenzensulfonyl)-4-(2-nitrophenyl)-1H-1,2,3-triazole
Conditions | Yield |
---|---|
With [Tpm*,BrCu(NCMe)]BF4 In chloroform at 40℃; for 72h; Inert atmosphere; | 99% |
4-toluenesulfonyl azide
propargyl benzene
4-benzyl-1-(p-tosyl)-1H-1,2,3-triazole
Conditions | Yield |
---|---|
With copper(I) thiophene-2-carboxylate; benzoic acid In benzene at 60℃; for 0.05h; Flow reactor; | 99% |
With copper(I) thiophene-2-carboxylate In toluene at 20℃; for 3h; | 75% |
4-toluenesulfonyl azide
1-ethynylcyclopentanol
1-(1-(p-tosyl)-1H-1,2,3-triazol-4-yl)cyclopentan-1-ol
Conditions | Yield |
---|---|
With copper(I) thiophene-2-carboxylate; benzoic acid In benzene at 60℃; for 0.05h; Flow reactor; | 99% |
With copper(I) thiophene-2-carboxylate In toluene at 20℃; for 3h; | 90% |
With copper(I) thiophene-2-carboxylate In toluene at 20℃; for 2h; | 83% |
4-toluenesulfonyl azide
4-(1-phenylvinyl)morpholine
4-methyl-N-[morpholino(phenyl)methylene]benzenesulfonamide
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 0.333333h; | 99% |
4-toluenesulfonyl azide
4-methoxyphenylacetylen
4-(4-methoxyphenyl)-1-tosyl-1H-1,2,3-triazole
Conditions | Yield |
---|---|
With copper(I) thiophene-2-carboxylate; benzoic acid In benzene at 60℃; for 0.05h; Flow reactor; | 99% |
With copper(II) acetate monohydrate; 2-amino-phenol In acetonitrile at 20℃; for 0.5h; regioselective reaction; | 96% |
With (N,N’-bis-{2,6-(di-iso-propyl)phenyl}imidazole-2-ylidene)tri-tert-butylphosphinetetrafluoroborate copper (I) In toluene at 20℃; for 15h; | 93% |
4-toluenesulfonyl azide
para-bromoacetophenone
N-(2-acetyl-5-bromophenyl)-4-methylbenzenesulfonamide
Conditions | Yield |
---|---|
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; lithium carbonate; acetic acid; silver(I) triflimide In 1,2-dichloro-ethane at 25℃; for 12h; Inert atmosphere; | 99% |
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; sodium acetate; silver(I) triflimide In 1,2-dichloro-ethane at 80℃; for 12h; | 71% |
With silver hexafluoroantimonate; [RhCl2(p-cymene)]2; copper(II) acetate monohydrate In 1,2-dichloro-ethane at 100℃; for 24h; Inert atmosphere; Schlenk technique; | 70% |
With silver hexafluoroantimonate; dichloro(p-cymene)ruthenium(II) dimer; copper diacetate In 1,2-dichloro-ethane at 80℃; for 48h; Inert atmosphere; | 46% |
4-toluenesulfonyl azide
acetophenone
N-(2-acetylphenyl)-4-methylbenzenesulfonamide
Conditions | Yield |
---|---|
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; lithium carbonate; acetic acid; silver(I) triflimide In 1,2-dichloro-ethane at 25℃; for 12h; Inert atmosphere; | 99% |
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; sodium acetate; silver(I) triflimide In 1,2-dichloro-ethane at 80℃; for 12h; Reagent/catalyst; Temperature; Time; | 97% |
With bromopentacarbonylmanganese(I); dimethyl zinc(II); copper diacetate In 1,4-dioxane; toluene at 0 - 80℃; for 6h; Schlenk technique; Inert atmosphere; regioselective reaction; | 90% |
With silver hexafluoroantimonate; dichloro(p-cymene)ruthenium(II) dimer; copper diacetate In 1,2-dichloro-ethane at 80℃; for 24h; Inert atmosphere; | 75% |
With silver hexafluoroantimonate; [RhCl2(p-cymene)]2; copper(II) acetate monohydrate In 1,2-dichloro-ethane at 100℃; for 24h; Solvent; Reagent/catalyst; Inert atmosphere; Schlenk technique; | 72% |
4-toluenesulfonyl azide
benzoic acid ethyl ester
ethyl 2-(4-methylphenylsulfonamido)benzoate
Conditions | Yield |
---|---|
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; lithium carbonate; acetic acid; silver(I) triflimide In 1,2-dichloro-ethane at 50℃; for 12h; Temperature; Reagent/catalyst; Solvent; Inert atmosphere; | 99% |
4-toluenesulfonyl azide
5-bromo-N-acetylindoline
N-(1-acetyl-5-bromoindolin-7-yl)-4-methylbenzenesulfonamide
Conditions | Yield |
---|---|
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; silver(I) triflimide In 1,2-dichloro-ethane at 20℃; for 3h; | 99% |
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; sodium acetate; silver(I) triflimide In 1,2-dichloro-ethane at 25℃; for 6h; Inert atmosphere; regioselective reaction; | 95% |
With silver hexafluoroantimonate; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; silver(I) acetate In 1,2-dichloro-ethane at 80℃; for 10h; Schlenk technique; | 75% |
4-toluenesulfonyl azide
4-methylphenylboronic acid
4-methyl-N-(4-methylphenyl)benzenesulfonamide
Conditions | Yield |
---|---|
With copper(l) chloride In methanol at 20℃; for 0.5h; Chan-Lam Coupling; | 99% |
With L-proline-functionalized MCM-41-immobilized-CuCl; air In methanol at 20℃; for 2h; | 97% |
With Copper(II) immobilized into prolinamide-modified polyacrylonitrile fiber In methanol at 60℃; for 0.5h; Chan-Lam Coupling; | 94% |
With air; Graphene supported-1-N-ferrocenylmethylimidazole-Copper complex In ethanol at 70℃; for 0.75h; Catalytic behavior; | 92% |
Conditions | Yield |
---|---|
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; lithium carbonate; acetic acid; silver(I) triflimide In 1,2-dichloro-ethane at 80℃; for 12h; Inert atmosphere; | 99% |
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; sodium acetate; silver(I) triflimide In 1,2-dichloro-ethane at 80℃; for 16h; Catalytic behavior; Reagent/catalyst; Solvent; Sealed tube; | 92% |
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; lithium acetate; silver(I) triflimide In 1,2-dichloro-ethane at 50℃; for 24h; | 88% |
4-toluenesulfonyl azide
Conditions | Yield |
---|---|
With copper(I) thiophene-2-carboxylate In toluene at 20℃; Schlenk technique; Inert atmosphere; | 99% |
4-toluenesulfonyl azide
Conditions | Yield |
---|---|
With [Cp*Ir(OCOCH3)2]; silver(I) triflimide In 1,2-dichloro-ethane at 25℃; for 12h; regioselective reaction; | 99% |
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; silver(I) acetate; silver(I) triflimide In 1,2-dichloro-ethane at 80℃; Sealed tube; Inert atmosphere; regioselective reaction; | 78% |
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; lithium acetate; silver(I) triflimide In 1,2-dichloro-ethane at 120℃; for 1h; regioselective reaction; | 76% |
4-toluenesulfonyl azide
Conditions | Yield |
---|---|
With copper(I) thiophene-2-carboxylate In toluene at 0 - 20℃; for 1h; Inert atmosphere; Schlenk technique; | 99% |
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