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:271-34-1
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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
Cas:271-34-1
Min.Order:1 Metric Ton
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inquiryT he company has advanced technology, as well as a large number of excellent R & D team, to provide customers from the grams to one hundred kilograms and tons of high-quality products, competitive prices and quality service Appearance:W
1. Factory price and high quality must be guaranteed, base on 8 years of production and R&D experience2. Free samples will be provided,ensure specifications and quality are right for customer3. Customers will receive the most professional technical s
Cas:271-34-1
Min.Order:1 Gram
FOB Price: $0.1
Type:Manufacturers
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
5-Azaindole Basic information Product Name: 5-Azaindole Synonyms: HARMYRINE;1H-PYRROLO[3,2-C]PYRIDINE;1,6-DIAZAINDENE;1,5-DIAZAINDENE;5-AZAINDOLE;3,7-DIDEAZAPURINE;5-AZAINDOLE 98%;1H-Pyr
Product Description Product website: http://www.finerchem.com Product Name 5-Azaindole CAS No. 271-34-1 Ass
With 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
Cas:271-34-1
Min.Order:1 Kilogram
FOB Price: $5.0 / 10.0
Type:Trading Company
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:271-34-1
Min.Order:1 Kilogram
FOB Price: $139.0 / 210.0
Type:Trading Company
inquiry1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; Appearance:Powder Storage:Store in sealed containers at cool & dry pla
Cas:271-34-1
Min.Order:100 Gram
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Type:Other
inquiry1.In No Less 10 years exporting experience. you can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specializ
5-Azaindole CAS:271-34-1 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 intermediates,
Cas:271-34-1
Min.Order:1 Gram
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Type:Lab/Research institutions
inquiryAdvantage : LIDE PHARMACEUTICALS LTD. is a mid-small manufacturing-type enterprise, engaged in pharmaceutical intermediates of R&D, custom-made and production, and also involving trading chemicals for export. We have established the R&
Cas:271-34-1
Min.Order:0
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Type:Lab/Research institutions
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
Best quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
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
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
Cas:271-34-1
Min.Order:4 Kilogram
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Type:Lab/Research institutions
inquiryThe 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
1. Product advantages: exquisite appearance and unique functions. 2. Product Advantages: Our products are the best,fast speed ,in large stock 3. High-quality products and thoughtful service are your greatest satisfaction. 4. The product
Our advantages: 1, High quality with competitive price: 1) Standard:BP/USP/EP/Enterprise standard 2) All Purity≥99% 3) We are manufacturer and can provide high quality products with factory price. 2, Fast and safe delivery 1) Parcel can be
Cas:271-34-1
Min.Order:1 Gram
Negotiable
Type:Other
inquiryMassive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and
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
Established in May 2015, TaiChem Ltd. is initially invested by a British research and development company and started by PhDs back from aboard. The company is registered in China Medical City (CMC), Taizhou, Jiangsu Province, and the production site
Product Name: 5-Azaindole Synonyms: 5-Azaindole ,98%;5-Azaindole,1H-pyrrolo[3,2-c]pyridine;5-Aza-1H-indole;5-Azaindole (1,5-Diazaindene 3,7-Dideazapurine);HARMYRINE;1H-PYRROLO[3,2-C]PYRIDINE;1,6-DIAZAINDENE;1,5-DIAZAINDENE CAS: 271-34-1 MF:
Cas:271-34-1
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryfactory?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
We Huarong Pharm can provide Customized Synthesis & Process R&D & APIs and intermediates Production & Quality Research & Registration Application, especially our GMP validation service which complies with SFDA, FDA, WHO and EU EMPA. O
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
Product name: 5-azaindole. Synonyms:5-Azaindole,98%;5-Azaindole,1H-pyrrolo[3,2-c]pyridine;5-Aza-1H-indole;5-Azaindole(1,5-Diazaindene3,7-DideaChemicalbookzapurine);HARMYRINE;1H-PYRROLO[3,2-C]PYRIDINE;1,6-DIAZAINDENE;1,5-DIAZAINDENE CAS No: 271-
Located in Hangzhou National Hi-Tech Industrial Development Zone, zhongqichem is a technical company mainly focus on the Custom synthesis, manufacturing, sales of chemicals to various industries. Benefiting from the outstanding customer service and h
4-chloro-1H-pyrrolo-[3,2-c]-pyridine
5-azaindole
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol | 96% |
tert-butyl 1H-pyrrolo[3,2-c]pyridine-1-carboxylate
5-azaindole
Conditions | Yield |
---|---|
With trifluoroacetic acid In dichloromethane at 20℃; for 1.5h; | 95% |
3-(4-Morpholinovinylene)-4-nitropyridine 1-oxide
5-azaindole
Conditions | Yield |
---|---|
With hydrogen; nickel In ethanol; water under 14.7 - 22.07 Torr; 1) 15 h, 20 deg C, 2) 3-5 h, 60 deg C; | 92% |
3-Dimethylaminovinylene-4-nitropyridine
5-azaindole
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol under 14.7 - 22.07 Torr; 1) 1 h, 20 deg C, 2) 3 h, 60 deg C; | 91% |
(E)-N,N-dimethyl-2-(4-nitro-1-oxidopyridin-3-yl)ethenamine
5-azaindole
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In ethanol at 60℃; under 3750.38 Torr; for 4h; Inert atmosphere; | 91% |
With hydrogen; palladium on activated charcoal In ethanol under 14.7 - 22.07 Torr; 1) 1 h, 20 deg C, 2) 3 h, 60 deg C; | 87% |
With hydrogen; Raney nickel In ethanol; water at 20 - 40℃; under 750.075 Torr; for 5.25h; | 76% |
Conditions | Yield |
---|---|
With Ni(1,5-cyclooctadiene)2 In tetrahydrofuran; diethyl ether at 110℃; for 4.5h; Temperature; Microwave irradiation; | 90.4% |
N-(3-((Z)-2-ethoxyvinyl)pyridin-4-yl)acetamide
5-azaindole
Conditions | Yield |
---|---|
With hydrogenchloride In methanol for 2h; Heating; | 90% |
With hydrogenchloride In methanol; water for 5h; Inert atmosphere; Reflux; | 1.9 g |
5-azaindole
Conditions | Yield |
---|---|
In ethanol; water | 84% |
3-ethynyl-4-pyridinamine
5-azaindole
Conditions | Yield |
---|---|
With pyrrolidine In water at 200℃; for 0.25h; Microwave irradiation; | 82% |
3-dimethylaminovinylene-4-nitropyridine-l-oxide
5-azaindole
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In ethanol at 20 - 65℃; under 1500.15 - 2250.23 Torr; for 8h; Inert atmosphere; Autoclave; | 74.5% |
N-(3-methyl-[4]pyridyl)-formamide
sodium formate
sodium anilide
5-azaindole
Conditions | Yield |
---|---|
at 300℃; |
N-(3-methyl-[4]pyridyl)-formamide
5-azaindole
Conditions | Yield |
---|---|
With sodium formate; sodium anilide at 290 - 310℃; |
1H-pyrrole[3,2-C]pyridine-3-carboxylic acid
5-azaindole
(3-Trimethylsilanylethynyl-pyridin-4-yl)-carbamic acid ethyl ester
5-azaindole
Conditions | Yield |
---|---|
With sodium ethanolate In ethanol Heating; Yield given; |
5-azaindole
Conditions | Yield |
---|---|
With hydrogenchloride at 45 - 50℃; for 1h; Yield given; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: dimethylformamide / 90 °C 2: H2 / Pd/C / ethanol / 60 °C View Scheme | |
Multi-step reaction with 2 steps 1: N,N-dimethyl-formamide / 20 - 90 °C / Inert atmosphere 2: palladium 10% on activated carbon; hydrogen / ethanol / 4 h / 60 °C / 3750.38 Torr / Inert atmosphere View Scheme | |
Multi-step reaction with 2 steps 1: N,N-dimethyl-formamide / 1.5 h / 100 °C 2: palladium 10% on activated carbon; hydrogen / ethanol / 8 h / 20 - 65 °C / 1500.15 - 2250.23 Torr / Inert atmosphere; Autoclave View Scheme |
N-(4-pyridyl) t-butyl carbamate
5-azaindole
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 1.) BuLi / 1.) THF, hexane, 0 deg C, 3 h, 2.) THF, hexane, 20 deg C, 1 h 2: 1.) t-BuLi / 1.) THF, pentane, -40 deg C, 1 h, 2.) THF, pentane, 20 deg C, 1 h 3: 5.5 M HCl / 1 h / 45 - 50 °C View Scheme |
(3-methylpyridin-4-yl)carbamic acid tert-butyl ester
5-azaindole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) t-BuLi / 1.) THF, pentane, -40 deg C, 1 h, 2.) THF, pentane, 20 deg C, 1 h 2: 5.5 M HCl / 1 h / 45 - 50 °C View Scheme |
3-bromopyridin-4-amine
5-azaindole
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 2: 93 percent / Pd(PPh3)2Cl2, Et4NCl / acetonitrile / 2.5 h / Heating 3: 90 percent / conc. HCl / methanol / 2 h / Heating View Scheme | |
Multi-step reaction with 3 steps 1: 52 percent / pyridine / 3 h / 0-10 deg C 2: CUI, Et3N / Pd(PPh3)2Cl2 / 100 - 110 °C 3: NaOEt / ethanol / Heating View Scheme | |
Multi-step reaction with 3 steps 1: N-ethyl-N,N-diisopropylamine / dichloromethane / 16 h / 5 - 20 °C / Inert atmosphere 2: bis-triphenylphosphine-palladium(II) chloride; tetrabutyl-ammonium chloride / acetonitrile / 2.5 h / Inert atmosphere; Reflux 3: hydrogenchloride / methanol; water / 5 h / Inert atmosphere; Reflux View Scheme |
N-(3-bromopyridin-4-yl)acetamide
5-azaindole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 93 percent / Pd(PPh3)2Cl2, Et4NCl / acetonitrile / 2.5 h / Heating 2: 90 percent / conc. HCl / methanol / 2 h / Heating View Scheme | |
Multi-step reaction with 2 steps 1: bis-triphenylphosphine-palladium(II) chloride; tetrabutyl-ammonium chloride / acetonitrile / 2.5 h / Inert atmosphere; Reflux 2: hydrogenchloride / methanol; water / 5 h / Inert atmosphere; Reflux View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 75 percent / 20percent aq. TiCl3 / acetic acid / 25 h / Ambient temperature 3: 93 percent / Pd(PPh3)2Cl2, Et4NCl / acetonitrile / 2.5 h / Heating 4: 90 percent / conc. HCl / methanol / 2 h / Heating View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 63 percent / dimethylformamide / 1 h / 90 °C 2: 91 percent / H2 / 10percent Pd/C / ethanol / 14.7 - 22.07 Torr / 1) 1 h, 20 deg C, 2) 3 h, 60 deg C View Scheme | |
Multi-step reaction with 3 steps 1: palladium; ethanol / Hydrogenation 2: THF 3: sodium anilide; sodium formate / 290 - 310 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 81 percent / PCl3 / 3.5 h / T < 0 deg C 2: 63 percent / dimethylformamide / 1 h / 90 °C 3: 91 percent / H2 / 10percent Pd/C / ethanol / 14.7 - 22.07 Torr / 1) 1 h, 20 deg C, 2) 3 h, 60 deg C View Scheme | |
Multi-step reaction with 2 steps 1: 92 percent / dimethylformamide / 2 h / 100 °C 2: 92 percent / H2 / Raney nickel / ethanol; H2O / 14.7 - 22.07 Torr / 1) 15 h, 20 deg C, 2) 3-5 h, 60 deg C View Scheme | |
Multi-step reaction with 2 steps 1: 96 percent / dimethylformamide / 1 h / 90 °C 2: 87 percent / H2 / 10percent Pd/C / ethanol / 14.7 - 22.07 Torr / 1) 1 h, 20 deg C, 2) 3 h, 60 deg C View Scheme |
ethyl (3-bromopyridin-4-yl)carbamate
5-azaindole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: CUI, Et3N / Pd(PPh3)2Cl2 / 100 - 110 °C 2: NaOEt / ethanol / Heating View Scheme |
1-benzyl-4,5-dihydro-4-oxopyrrolo<3,2-c>pyridine
5-azaindole
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 79 percent / Na, liquid ammonia 2: 78 percent / phosphorus oxychloride / 5 h / 180 °C 3: 96 percent / H2 / 10percent Pd/C / ethanol View Scheme |
4,5-dihydro-4-oxo-1H-pyrrolo<3,2-c>pyridine
5-azaindole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 78 percent / phosphorus oxychloride / 5 h / 180 °C 2: 96 percent / H2 / 10percent Pd/C / ethanol View Scheme |
4-amino-3-methylpyridine
5-azaindole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: THF 2: sodium anilide; sodium formate / 290 - 310 °C View Scheme | |
Multi-step reaction with 3 steps 1: TiCl2(ClO4)2 / acetone / 1 h / 60 °C 2: salicylic acid; iron(II) oxide / N,N-dimethyl acetamide / 2 h / 70 °C 3: zinc(II) oxide / tetrachloromethane / 2 h / 90 °C View Scheme |
{[(3-Trimethylsilanyl)ethynyl]-pyridin-4-yl}amine
5-azaindole
Conditions | Yield |
---|---|
With copper(I) iodide In N,N-dimethyl-formamide |
3-methyl-4-nitropyridine N-oxide
N,N-dimethylformamide diethyl diacetal
5-azaindole
Conditions | Yield |
---|---|
With sodium hydroxide; ammonium formate; palladium In ethanol; water; N,N-dimethyl-formamide; toluene; benzene |
5-azaindole
di-tert-butyl dicarbonate
tert-butyl 1H-pyrrolo[3,2-c]pyridine-1-carboxylate
Conditions | Yield |
---|---|
With dmap In acetonitrile at 20℃; for 18h; | 100% |
With triethylamine In dichloromethane at 25℃; for 12h; Inert atmosphere; | 98.2% |
With triethylamine In dichloromethane at 25℃; for 12h; Inert atmosphere; | 98.2% |
5-azaindole
benzyl chloroformate
benzyl 1H-pyrrolo[3,2-c]pyridine-1-carboxylate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 1h; | 100% |
With triethylamine In dichloromethane at 0 - 20℃; for 1h; | 100% |
5-azaindole
6-bromo-4-chloro-2-(2-fluoro-phenyl)-quinazoline
6-bromo-2-(2-fluoro-phenyl)-4-pyrrolo[3,2-c]pyridin-1-yl-quinazoline
Conditions | Yield |
---|---|
With caesium carbonate In DMF (N,N-dimethyl-formamide) at 20℃; for 1h; | 98% |
5-azaindole
Conditions | Yield |
---|---|
With water-d2; silver trifluoromethanesulfonate In chloroform-d1 at 90℃; for 18h; regioselective reaction; | 97% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 140℃; for 6h; | 96% |
Conditions | Yield |
---|---|
With aluminium trichloride In dichloromethane at 20℃; Friedel-Crafts reaction; | 94% |
5-azaindole
p-toluenesulfonyl chloride
1-tosyl-1H-pyrrolo[3,2-c]pyridine
Conditions | Yield |
---|---|
With tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide In water; toluene at 0 - 10℃; for 2h; Inert atmosphere; | 93% |
Stage #1: 5-azaindole With sodium hydride In tetrahydrofuran; mineral oil at 0 - 20℃; for 1.16667h; Inert atmosphere; Stage #2: p-toluenesulfonyl chloride In tetrahydrofuran for 15h; |
Conditions | Yield |
---|---|
With aluminium trichloride In dichloromethane at 20℃; Friedel-Crafts reaction; | 92% |
Conditions | Yield |
---|---|
With tetrabutyl phosphonium bromide; potassium carbonate In water at 20℃; for 12h; regioselective reaction; | 92% |
5-azaindole
3-iodo-1H-pyrrolo[3,2-c]pyridine
Conditions | Yield |
---|---|
With potassium hydroxide; iodine In N,N-dimethyl-formamide at 20℃; for 0.25h; | 91% |
With iodine; potassium hydroxide regiospecific reaction; | 87% |
Stage #1: 5-azaindole With potassium hydroxide In N,N-dimethyl-formamide at 20℃; for 0.25h; Stage #2: With iodine In N,N-dimethyl-formamide at 0 - 20℃; for 0.25h; | 83% |
With iodine; potassium hydroxide In N,N-dimethyl-formamide at 20℃; | 73% |
Stage #1: 5-azaindole With potassium hydroxide In N,N-dimethyl-formamide at 25℃; for 0.25h; Stage #2: With iodine In N,N-dimethyl-formamide at 25℃; for 0.25h; |
5-azaindole
4-iodopyridine
1-(pyridin-4-yl)-1H-pyrrolo[3,2-c]pyridine
Conditions | Yield |
---|---|
With potassium phosphate In dimethyl sulfoxide at 80℃; for 5h; Ullmann-Goldberg Substitution; Inert atmosphere; | 90% |
With potassium phosphate; copper In dimethyl sulfoxide at 80℃; for 5h; Ullmann-Goldberg Substitution; Inert atmosphere; | 90% |
5-azaindole
o-nitroiodobenzene
1-(2-nitrophenyl)-1H-pyrrolo[3,2-c]pyridine
Conditions | Yield |
---|---|
With potassium phosphate; copper In dimethyl sulfoxide at 80℃; for 2h; Ullmann-Goldberg Substitution; Inert atmosphere; | 89% |
With potassium phosphate In dimethyl sulfoxide at 80℃; for 2h; Ullmann-Goldberg Substitution; Inert atmosphere; |
Conditions | Yield |
---|---|
With copper(l) iodide; potassium carbonate; lithium chloride In N,N-dimethyl-formamide at 120℃; for 24h; | 88% |
Conditions | Yield |
---|---|
With carbon dioxide; potassium hydroxide In acetonitrile at 130℃; for 12h; Autoclave; | 88% |
Conditions | Yield |
---|---|
With copper(l) iodide; potassium carbonate; lithium chloride In N,N-dimethyl-formamide at 120℃; for 24h; | 85% |
5-azaindole
methyl iodide
5-methyl-1H-pyrrolo[3,2-c]pyridin-5-ium iodide
Conditions | Yield |
---|---|
In toluene at 120℃; for 2h; Inert atmosphere; | 85% |
Conditions | Yield |
---|---|
With caesium carbonate In dimethyl sulfoxide at 100℃; for 3h; Schlenk technique; | 85% |
Conditions | Yield |
---|---|
Stage #1: 5-azaindole With potassium hydroxide In dimethyl sulfoxide at 20℃; for 0.5h; Schlenk technique; Stage #2: 2-Iodobenzyl bromide In dimethyl sulfoxide at 20℃; Schlenk technique; | 85% |
5-azaindole
benzenesulfonyl chloride
1-Benzenesulfonyl-1H-pyrrolo<3,2-c>pyridine
Conditions | Yield |
---|---|
Stage #1: 5-azaindole With sodium hydride In tetrahydrofuran at 20℃; for 0.5h; Stage #2: benzenesulfonyl chloride In tetrahydrofuran at 20℃; | 84% |
Stage #1: 5-azaindole With sodium hydride In mineral oil at 0℃; for 0.5h; Stage #2: benzenesulfonyl chloride at 0 - 20℃; for 1h; | 69.4% |
Stage #1: 5-azaindole With sodium hydride In tetrahydrofuran; mineral oil at 0℃; for 0.5h; Stage #2: benzenesulfonyl chloride In tetrahydrofuran at 0 - 20℃; for 1h; | 69.4% |
5-azaindole
2-mesitylenesulphonyl chloride
1-(2,4,6-trimethyl-benzenesulfonyl)-1H-pyrrolo[3,2-c]pyridine
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran at 0 - 25℃; for 16h; Inert atmosphere; | 84% |
With sodium hydride at 0 - 20℃; for 16h; | 84% |
5-azaindole
Conditions | Yield |
---|---|
In water at 80℃; Sealed tube; Green chemistry; regioselective reaction; | 84% |
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