Taizhou FremChem Co. Ltd. is a high-tech enterprise located in China Medical City specializing in R&D, manufacturing, sales of new APIS, pharmaceutical intermediates and fine chemicals. All of our company is committed to provide high quality chemical
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inquiryDayangchem'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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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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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
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
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inquiryCangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new ap
Colorcom is a global leader in industrial chemical manufacturing and is continuously innovating and transforming to exceed client expectations and industry standards. Colorcom prides itself on superior customer and technical focus, while focusing on
Our 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
Cas:4519-40-8
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inquiryCompetitive Price High Quality Fast Delivery custom-made Welcome to Henan Tianfu Chemical Co., Ltd. website. Our company engages in Sodium Tripolyphosphate (STPP) and Sodium Hexametabphosphate (SHMP) production; development of noble me
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inquiryOur advantages: 1. All inquiries will be replied within 12 hours. 2. Dedication to quality, supply & service. 3. Strictly on selecting raw materials. 4. Reasonable & competitive price, fast lead time. 5. Sample is available for your eva
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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
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inquiryroduct name 2,4-Difluoroaniline Product category Pharmaceutical intermediate CAS No. 367-25-9 Structual formula
Cas:4519-40-8
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inquiry1.No Less 8 years exporting experience. Clients 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 Specialized
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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 prese
Cas:4519-40-8
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inquiry2,3-Difluoroaniline CAS: 4519-40-8 Specificatio Item Standard Identification A.H-NMR:Comply with the structure B.LC-MS:Comply with the structure C.The IR spectrum
Cas:4519-40-8
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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
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
Company 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
Cas:4519-40-8
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inquiryHangzhou 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
Cas:4519-40-8
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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
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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inquiryChemlyte Solutions believe that customers and suppliers deserve much more than what traditional distributors can offer. To grow in today s fast-paced and increasingly competitive market it is essential to be able to quickly adapt to market forces eff
Cas:4519-40-8
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inquiryOur Advantages Production: Advanced chemical equipment with years of experience Staffs for producing various extract products. Quality Control:A complete set of Testing Professional and Analysis Equipment ensures the Quality Requirements and Specif
Cas:4519-40-8
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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
Cas:4519-40-8
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inquiryGMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,
2,3-Difluoroaniline Chemical Properties Boiling point 68-69 °C density 1.274 g/mL at 25 °C (lit.) refractive index n20/D 1.514(lit.) Fp 160 °F pka 2.19±0.10(Predicted) form Liquid Specific Gravity 1.274 co
Cas:4519-40-8
Min.Order:1 Gram
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Type:Lab/Research institutions
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
Cas:4519-40-8
Min.Order:1 Kilogram
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inquiryGOLDEN PHARMA CO.,LIMITED.is a professional pharmaceutical company,our team have more than 20years expereince in pharmaceutical production and sales. we are a professional technical enterprise specializing in the R & D, production,QA regulation
Our company is engaged in customizing the benzene ring and pyridine derivative organic intermediates, and the quantity is flexible according to customer's needs. It mainly provides high-quality intermediates for domestic and foreign pharmaceutical an
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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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inquiry2,3-difluoroanilline
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen; triethylamine In methanol at 50℃; for 3h; | 98% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen; triethylamine In methanol at 50℃; for 2.5h; Temperature; | 93% |
2,3-difluoroanilline
Conditions | Yield |
---|---|
With hydrogenchloride In water for 1h; Reflux; | 89.1% |
2,3-difluoroanilline
Conditions | Yield |
---|---|
Stage #1: 1-(6-amino-2,3-difluorophenyl)pyrrolidine-2,5-dione With sulfuric acid; acetic acid; sodium nitrite at 5℃; for 0.5h; Stage #2: With ethanol; zinc for 1.5h; Reflux; | 83.6% |
Multi-step reaction with 2 steps 1.1: sodium nitrite; sulfuric acid; acetic acid / 0.5 h / 5 °C 1.2: 1 h / 50 °C 2.1: hydrogenchloride / water / 1 h / Reflux View Scheme |
Conditions | Yield |
---|---|
With ammonium hydroxide; cesium fluoride; copper(I) oxide 1.) N,N'-dimethylethyleneurea, 250 deg C (bomb), 12 h, 2.) 170 deg C (bomb), 24 h; Yield given. Multistep reaction. Further byproducts given. Yields of byproduct given; | |
With ammonium hydroxide; cesium fluoride; copper(I) oxide 1.) N,N'-dimethylethyleneurea, 250 deg C (bomb), 12 h, 2.) 160 deg C (bomb), 24 h; Yield given. Multistep reaction. Further byproducts given. Yields of byproduct given; |
Conditions | Yield |
---|---|
With hydrogen; sodium formate; palladium on charcoal |
difluorodichlorobenzene
1-chloro-3,5-difluorobenzene
3,4,5-trichloro-2,6-difluoronitrobenzene
1,2,4-trichloro-3,5-difluoronitrobenzene
2,3-difluoroanilline
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid; sodium acetate; chlorine; aluminium trichloride; palladium on charcoal In methanol; dichloromethane |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: iron; bromine / 4.83 h / 20 - 50 °C 2: sulfuric acid; nitric acid / water / 1.5 h / 20 - 35 °C 3: palladium 10% on activated carbon; hydrogen; triethylamine / methanol / 2.5 h / 50 °C View Scheme | |
Multi-step reaction with 4 steps 1: iron; bromine / 4.83 h / 20 - 50 °C 2: sulfuric acid; nitric acid / water / 1.5 h / 20 - 35 °C 3: iron; calcium chloride; ethanol; water / 3.2 h / 55 °C 4: palladium 10% on activated carbon; hydrogen; triethylamine / methanol / 3 h / 50 °C View Scheme |
1,2-difluoro-4,5-dibromobenzene
2,3-difluoroanilline
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sulfuric acid; nitric acid / water / 1.5 h / 20 - 35 °C 2: palladium 10% on activated carbon; hydrogen; triethylamine / methanol / 2.5 h / 50 °C View Scheme | |
Multi-step reaction with 3 steps 1: sulfuric acid; nitric acid / water / 1.5 h / 20 - 35 °C 2: iron; calcium chloride; ethanol; water / 3.2 h / 55 °C 3: palladium 10% on activated carbon; hydrogen; triethylamine / methanol / 3 h / 50 °C View Scheme |
A
2,3-difluoroanilline
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen; triethylamine In methanol at 45℃; for 4.2h; Temperature; |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: iron(III) chloride; chlorine / 9 h / 48 - 54 °C 2: sulfuric acid; nitric acid / water / 7 h / 20 - 26 °C 3: palladium 10% on activated carbon; hydrogen; triethylamine / methanol / 4.2 h / 45 °C View Scheme |
A
2,3-difluoroanilline
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sulfuric acid; nitric acid / water / 7 h / 20 - 26 °C 2: palladium 10% on activated carbon; hydrogen; triethylamine / methanol / 4.2 h / 45 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: potassium carbonate / N,N-dimethyl-formamide / 6 h / 20 °C 2.1: hydrogen; palladium 10% on activated carbon / methanol / 4 h / 20 °C / Inert atmosphere 3.1: sodium nitrite; sulfuric acid; acetic acid / 0.5 h / 5 °C 3.2: 1.5 h / Reflux View Scheme | |
Multi-step reaction with 4 steps 1.1: ammonium hydroxide / ethanol / 8 h / 20 °C 2.1: toluene-4-sulfonic acid / 5,5-dimethyl-1,3-cyclohexadiene / 7 h / Dean-Stark; Reflux 3.1: hydrogen; palladium 10% on activated carbon / methanol / 4 h / 20 °C / Inert atmosphere 4.1: sodium nitrite; sulfuric acid; acetic acid / 0.5 h / 5 °C 4.2: 1.5 h / Reflux View Scheme | |
Multi-step reaction with 4 steps 1.1: potassium carbonate / N,N-dimethyl-formamide / 6 h / 20 °C 2.1: hydrogen; palladium 10% on activated carbon / methanol / 4 h / 20 °C / Inert atmosphere 3.1: sodium nitrite; sulfuric acid; acetic acid / 0.5 h / 5 °C 3.2: 1 h / 50 °C 4.1: hydrogenchloride / water / 1 h / Reflux View Scheme | |
Multi-step reaction with 5 steps 1.1: ammonium hydroxide / ethanol / 8 h / 20 °C 2.1: toluene-4-sulfonic acid / 5,5-dimethyl-1,3-cyclohexadiene / 7 h / Dean-Stark; Reflux 3.1: hydrogen; palladium 10% on activated carbon / methanol / 4 h / 20 °C / Inert atmosphere 4.1: sodium nitrite; sulfuric acid; acetic acid / 0.5 h / 5 °C 4.2: 1 h / 50 °C 5.1: hydrogenchloride / water / 1 h / Reflux View Scheme |
2-amino-3,4-difluoronitro-benzene
2,3-difluoroanilline
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: toluene-4-sulfonic acid / 5,5-dimethyl-1,3-cyclohexadiene / 7 h / Dean-Stark; Reflux 2.1: hydrogen; palladium 10% on activated carbon / methanol / 4 h / 20 °C / Inert atmosphere 3.1: sodium nitrite; sulfuric acid; acetic acid / 0.5 h / 5 °C 3.2: 1.5 h / Reflux View Scheme | |
Multi-step reaction with 4 steps 1.1: toluene-4-sulfonic acid / 5,5-dimethyl-1,3-cyclohexadiene / 7 h / Dean-Stark; Reflux 2.1: hydrogen; palladium 10% on activated carbon / methanol / 4 h / 20 °C / Inert atmosphere 3.1: sodium nitrite; sulfuric acid; acetic acid / 0.5 h / 5 °C 3.2: 1 h / 50 °C 4.1: hydrogenchloride / water / 1 h / Reflux View Scheme |
2,3-difluoroanilline
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: hydrogen; palladium 10% on activated carbon / methanol / 4 h / 20 °C / Inert atmosphere 2.1: sodium nitrite; sulfuric acid; acetic acid / 0.5 h / 5 °C 2.2: 1.5 h / Reflux View Scheme | |
Multi-step reaction with 3 steps 1.1: hydrogen; palladium 10% on activated carbon / methanol / 4 h / 20 °C / Inert atmosphere 2.1: sodium nitrite; sulfuric acid; acetic acid / 0.5 h / 5 °C 2.2: 1 h / 50 °C 3.1: hydrogenchloride / water / 1 h / Reflux View Scheme |
2,3-difluoroanilline
potassium ethyl xanthogenate
2-mercapto-7-fluorobenzothiazole
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 4h; Inert atmosphere; Heating; | 100% |
In N,N-dimethyl-formamide at 100℃; for 4h; Inert atmosphere; | 100% |
In N,N-dimethyl-formamide at 160℃; for 4h; | 89% |
2-(3-((7-(benzyloxy)quinazolin-4-yl)amino)-1H-pyrazol-5-yl)acetic acid
2,3-difluoroanilline
2-(3-{[7-(benzyloxy)quinazolin-4-yl]amino}-1H-pyrazol-5-yl)-N-(2,3-difluorophenyl)acetamide
Conditions | Yield |
---|---|
With pyridine; trichlorophosphate at 0 - 20℃; for 2h; | 100% |
2,3-difluoroanilline
4-bromo-2,3-difluoro-aniline
Conditions | Yield |
---|---|
With N-Bromosuccinimide In N,N-dimethyl-formamide for 1h; Cooling with ice; | 100% |
With N-Bromosuccinimide In N,N-dimethyl-formamide at 0℃; for 1h; | 97% |
With N-Bromosuccinimide In acetonitrile at 35℃; for 2h; | 68% |
2,3-difluoroanilline
2,3-difluorobenzenesulphonyl chloride
Conditions | Yield |
---|---|
Stage #1: 2,3-difluoroanilline With hydrogenchloride; sodium nitrite In water at -5 - 0℃; for 0.166667h; Ice/NaCl; Stage #2: With thionyl chloride; copper(l) chloride In water at -5℃; for 0.5h; | 98% |
With hydrogenchloride; acetic acid; mercury; sodium nitrite; copper(I) chloride In water | |
Stage #1: 2,3-difluoroanilline With hydrogenchloride; sodium nitrite In water at -10℃; for 0.666667h; Stage #2: With hydrogenchloride; sulfur dioxide; copper(l) chloride In water; acetic acid at 0℃; | |
Stage #1: 2,3-difluoroanilline With hydrogenchloride; acetic acid; sodium nitrite In water at -5℃; Stage #2: With sulfur dioxide; copper(l) chloride In water for 0.25h; Cooling with ice; | |
Stage #1: 2,3-difluoroanilline With hydrogenchloride; sodium nitrite In water at -10℃; for 0.666667h; Stage #2: With sulfur dioxide; copper(l) chloride In water; acetic acid at 0℃; |
1-methanesulfonyl-1H-pyrrole-2,4-dicarboxylic acid 2-methyl ester
2,3-difluoroanilline
4-(2,3-difluoro-phenylcarbamoyl)-1-methanesulfonyl-1H-pyrrole-2-carboxylic acid methyl ester
Conditions | Yield |
---|---|
Stage #1: 1-methanesulfonyl-1H-pyrrole-2,4-dicarboxylic acid 2-methyl ester With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃; for 1h; Stage #2: 2,3-difluoroanilline With triethylamine In dichloromethane for 1h; | 98% |
4-chloro-3-formylcoumarin
2,3-difluoroanilline
7,8-difluoro-4-(2-hydroxyphenyl)quinoline-3-carboxylic acid
Conditions | Yield |
---|---|
With sulfuric acid In methanol at 20℃; for 0.0833333h; | 98% |
Conditions | Yield |
---|---|
In diethylene glycol dimethyl ether at 130℃; for 15h; | 97.9% |
2,3-difluoroanilline
2-(4-nitro-1H-pyrazol-1-yl)acetic acid
N-(2,3-difluorophenyl)-2-(4-nitro-1H-pyrazol-1-yl)acetamide
Conditions | Yield |
---|---|
With pyridine; trichlorophosphate In dichloromethane for 2h; | 97% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 2h; Heating; | 96% |
In 1-methyl-pyrrolidin-2-one at 120℃; |
ethylxanthogenate
2,3-difluoroanilline
2-mercapto-7-fluorobenzothiazole
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 120℃; for 2h; | 96% |
2,3-difluoroanilline
aminosulfonic acid
acrylic acid
2,4-Difluorocinnamic acid
Conditions | Yield |
---|---|
With sulfuric acid; sodium nitrite; palladium diacetate In water | 95% |
4-chloro-3-formylcoumarin
2,3-difluoroanilline
10,11-difluoro-6H-chromeno[4,3-b]quinolin-6-one
Conditions | Yield |
---|---|
In ethanol at 20℃; for 0.25h; ultrasound irradiation; | 94% |
In methanol at 20℃; for 0.15h; ultrasound irradiation; | 92% |
With Amberlyst-15 In ethanol for 2h; Reflux; Inert atmosphere; | 78% |
2,3-difluoroanilline
Conditions | Yield |
---|---|
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide In dichloromethane; ethyl acetate at 20℃; for 17h; | 92% |
2,3-difluoroanilline
Conditions | Yield |
---|---|
With chloro(2-dicyclohexylphosphino-2’,4’,6’-triisopropyl-1,1‘-biphenyl)[2-(2’-amino-1,1‘-biphenyl’)]palladium(II); sodium t-butanolate In 1,4-dioxane at 90℃; for 0.75h; Buchwald-Hartwig Coupling; Microwave irradiation; | 92% |
Conditions | Yield |
---|---|
Stage #1: 2,3-difluoroanilline; glycerol With sulfuric acid; sodium iodide at 150 - 180℃; for 4h; Stage #2: With sodium hydroxide In water at 60 - 70℃; | 91% |
Stage #1: 2,3-difluoroanilline With sulfuric acid at 0 - 20℃; for 1h; Stage #2: glycerol With sodium iodide at 150 - 180℃; for 3h; | 91% |
With sulfuric acid; sodium 3-nitrobenzenesulfonate at 140℃; for 4h; Condensation; cyclization; | 86% |
With sulfuric acid; sodium 3-nitrobenzenesulfonate In water at 135℃; | |
Stage #1: 2,3-difluoroanilline; glycerol With sulfuric acid; sodium 3-nitrobenzenesulfonate In water at 135℃; for 3.5h; Stage #2: With sodium hydroxide In water at 0 - 20℃; |
2,3-difluoroanilline
2-Bromoacetyl bromide
2-bromo-N-(2,3-difluorophenyl)acetamide
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether at 5 - 20℃; for 1h; | 91% |
With sodium hydroxide In diethyl ether; water at 5 - 20℃; for 1.33333h; | 91% |
With potassium carbonate In dichloromethane for 5h; | |
With potassium carbonate In dichloromethane for 5h; |
2,3-difluoroanilline
Conditions | Yield |
---|---|
With chloro(2-dicyclohexylphosphino-2’,4’,6’-triisopropyl-1,1‘-biphenyl)[2-(2’-amino-1,1‘-biphenyl’)]palladium(II); sodium t-butanolate In 1,4-dioxane at 90℃; for 0.75h; Buchwald-Hartwig Coupling; Inert atmosphere; Microwave irradiation; Sealed tube; | 91% |
2,3-difluoroanilline
1,2,3-thiadiazole-5-carbonyl azide
Conditions | Yield |
---|---|
In toluene Heating; | 90% |
2,3-difluoroanilline
chloroacetyl chloride
2-chloro-N-(2,3-difluorophenyl)acetamide
Conditions | Yield |
---|---|
With sodium hydroxide In diethyl ether; water at 5 - 20℃; for 1.33333h; | 90% |
With sodium hydroxide In diethyl ether; water at 5 - 20℃; for 1.33333h; | 90% |
Stage #1: 2,3-difluoroanilline With sodium hydrogencarbonate In chloroform at 20℃; for 0.25h; Stage #2: chloroacetyl chloride In chloroform at 20℃; for 2h; |
2,3-difluoroanilline
3-methyl-4-nitro-benzoyl chloride
N-(2,3-difluoro-phenyl)-3-methyl-4-nitro-benzamide
Conditions | Yield |
---|---|
With pyridine for 1h; Heating; | 89% |
2-(3-((7-(3-chloropropoxy)quinazolin-4-yl)amino)-1H-pyrazol-5-yl)acetic acid
2,3-difluoroanilline
2-(5-{[7-(3-chloropropoxy)quinazolin-4-yl]amino}-2H-pyrazol-3-yl)-N-(2,3-difluorophenyl)acetamide
Conditions | Yield |
---|---|
With pyridine; trichlorophosphate at 0 - 20℃; | 89% |
With pyridine; trichlorophosphate In diethyl ether; ethyl acetate at 0 - 20℃; for 23.5h; | 89% |
4-(piperidin-1-yl)benzaldehyde
2,3-difluoroanilline
N-(4-(piperidin-1-yl)benzylidene)-2,3-difluorobenzenamine
Conditions | Yield |
---|---|
With acetic acid In ethanol at 20℃; for 0.5h; | 88% |
Conditions | Yield |
---|---|
With sodium tris(acetoxy)borohydride; acetic acid In dichloromethane at 20℃; for 12h; | 88% |
2,3-difluoroanilline
2-chloro-2-(diethoxymethyl)-3-methyloxirane
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In water; toluene at 40℃; for 36h; Temperature; | 88% |
bis(benzonitrile)palladium(II) chloride
2,3-difluoroanilline
trans-[PdCl2(2,3-difluoroaniline)2]
Conditions | Yield |
---|---|
In ethanol under N2; soln. of PdCl2(C6H5CN)2 (0.26 mmol) added to soln. of 2,3-difluoroaniline (0.52 mmol); refluxed (8 h); hot soln. filtered; solvent removed (vac.); elem. anal.; | 87% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 20℃; for 16h; Inert atmosphere; | 87% |
[2-(tritylamino)-1,3-thiazol-5-yl]acetic acid
2,3-difluoroanilline
N-(2,3-difluorophenyl)-2-[2-(tritylamino)-1,3-thiazol-5-yl]acetamide
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 50℃; for 18h; | 85% |
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