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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inquiry4-(Butylamino)-benzoic acid, methyl ester CAS:71839-12-8 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
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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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inquiry1. Product advantages High purity, all above 98.5%, no impurities after dissolution We will test each batch to ensure quality OEM and private brand services designed for free Various cap colors available We can also provide MT1 peptide powd
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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
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inquiry1.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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inquiryR & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
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inquiryJ&H CHEM is one of China's leading providers of integrated fine chemical services including offering, research and development, Custom manufacturing business, as well as other Value-added customer services, for diversified range products of chemicals
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inquiry1.Our services:A.Supply sampleB.The packing also can be according the customers` requirmentC.Any inquiries will be replied within 24 hoursD.we provide Commerical Invoice, Packing List, Bill of loading, COA , Health certificate and Origin certificate.
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inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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inquirymethyl 4-(butylamino)benzoate CAS NO.71839-12-8 Application:methyl 4-(butylamino)benzoate CAS NO.71839-12-8
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inquiryfactory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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inquiryBest quality with low price Storage:ln stock Package:25kg/Barrel Application:Chemicals Transportation:Express/Sea/Air Port:Shanghai
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inquiryGood Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen
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inquiry*stable and better quality products*efficient and meticulous servicesAppearance:Powder Storage:Store in dry, cool and ventilated place Package:10G/bottle 1kg/tin 5kg/tin 25kg/carton Application:1. Chemical raw materials 2. Used as an analytical reage
methyl 4-(butylamino)benzoate CAS NO.71839-12-8Appearance:powder Storage:Dry and ventilated Package:Standard or as customer's require Application:intermediates Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By air(
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inquiryBest Seller, High Quality, Competitive Price, Fast Delivery, Quick ResponseAppearance:powder, or liquid Storage:Stored in room temperature, ventilated place Package:Bottle, barrel, cargo, container, etc. Application:Pharmaceuticals, intermediates, AP
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inquirytri-n-butylindium
A
o-benzenedisulfonimide
B
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
In tetrahydrofuran at 20 - 25℃; | A n/a B 92% |
Methyl 4-chlorobenzoate
N-butylamine
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
With di-tert-butyl{2′-isopropoxy-[1,1′-binaphthalen]-2-yl}phosphane; caesium carbonate; palladium diacetate In 1,2-dimethoxyethane at 110℃; for 16h; | 91% |
With 1,4-diaza-bicyclo[2.2.2]octane; nickel(II) bromide dimethoxyethane; tris(2,2-bipyridine)ruthenium(II) hexafluorophosphate In dimethyl sulfoxide at 80℃; for 1h; Flow reactor; Sealed tube; Schlenk technique; Inert atmosphere; Irradiation; | 65% |
methyl 4-iodobenzoate
N-butylamine
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
Stage #1: methyl 4-iodobenzoate With copper(l) iodide; L-proline In dimethyl sulfoxide at 20℃; for 0.0833333h; Ullmann-Goldberg Substitution; Inert atmosphere; Stage #2: N-butylamine In dimethyl sulfoxide at 20℃; for 17h; Ullmann-Goldberg Substitution; Inert atmosphere; | 91% |
methyl 4-butyramidobenzoate
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
With borane-ammonia complex; boron trifluoride diethyl etherate; tris(pentafluorophenyl)borate In 1,2-dichloro-ethane at 60℃; for 16h; | 84% |
n-butyllithium
C12H16N2O2S
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
In diethyl ether; hexane at -78 - 25℃; for 0.833333h; | 67% |
N-butylamine
4-methoxycarbonyl aniline
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
With palladium on activated charcoal In tetrahydrofuran at 170℃; for 1.5h; Microwave irradiation; | 34% |
Stage #1: N-butylamine; 4-methoxycarbonyl aniline In ethanol for 2h; Reflux; Stage #2: With sodium tetrahydroborate In methanol at 0 - 20℃; for 2h; | 30% |
methanol
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
With diethyl ether |
butyraldehyde
4-methoxycarbonyl aniline
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
With acetic acid; zinc; benzene |
methanol
4-(N-butylamino)benzoic acid
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
With sulfuric acid Heating; |
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: NaOMe / methanol 1.2: 80 percent / methanol / 0.5 h / 20 - 25 °C 2.1: 67 percent / diethyl ether; hexane / 0.83 h / -78 - 25 °C View Scheme |
4-methoxycarbonyl aniline
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: triethylamine / dichloromethane / 14 h / 0 - 20 °C 2: caesium carbonate / N,N-dimethyl-formamide / 2 h / 90 °C 3: potassium carbonate / methanol / 1 h / 70 °C View Scheme |
methyl 4-(2,2,2-trifluoroacetamido)benzoate
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: caesium carbonate / N,N-dimethyl-formamide / 2 h / 90 °C 2: potassium carbonate / methanol / 1 h / 70 °C View Scheme |
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
With potassium carbonate In methanol at 70℃; for 1h; | 702.6 mg |
methyl 4-butyramidobenzoate
A
N-(n-butyl)-4-methoxycarbonylaniline
B
4-methoxycarbonyl aniline
Conditions | Yield |
---|---|
With [bis(2-methylallyl)cycloocta-1,5-diene]ruthenium(II); formic acid; bis(trifluoromethanesulfonyl)amide; triethylamine; [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine] In dibutyl ether at 130℃; for 24h; Overall yield = 83 percent; Overall yield = 43 mg; |
2-bromo-1-cycloheptene-1-carboxylic acid
N-(n-butyl)-4-methoxycarbonylaniline
methyl 4-(2-bromo-N-butylcyclohept-1-ene-1-carboxamido)benzoate
Conditions | Yield |
---|---|
Stage #1: 2-bromo-1-cycloheptene-1-carboxylic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃; for 0.166667h; Stage #2: N-(n-butyl)-4-methoxycarbonylaniline With dmap In dichloromethane at 60℃; for 2h; | 97% |
2-bromo-1-cyclopentene-1-carboxylic acid
N-(n-butyl)-4-methoxycarbonylaniline
methyl 4-(2-bromo-N-butylcyclopent-1-ene-1-carboxamido)benzoate
Conditions | Yield |
---|---|
Stage #1: 2-bromo-1-cyclopentene-1-carboxylic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃; for 0.166667h; Stage #2: N-(n-butyl)-4-methoxycarbonylaniline With dmap In dichloromethane at 60℃; for 2h; | 92% |
Conditions | Yield |
---|---|
With [m-(1,4-diazabicyclo[2.2.2]octanekN1:kN4)]hexamethyldialuminum In tetrahydrofuran at 130℃; for 0.133333h; Inert atmosphere; Microwave irradiation; | 91% |
Conditions | Yield |
---|---|
With [m-(1,4-diazabicyclo[2.2.2]octanekN1:kN4)]hexamethyldialuminum In tetrahydrofuran at 130℃; for 0.133333h; Inert atmosphere; Microwave irradiation; | 89% |
2-bromocyclohex-1-enecarboxylic acid
N-(n-butyl)-4-methoxycarbonylaniline
methyl 4-(2-bromo-N-butylcyclohex-1-ene-1-carboxamido)benzoate
Conditions | Yield |
---|---|
Stage #1: 2-bromocyclohex-1-enecarboxylic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃; for 0.166667h; Stage #2: N-(n-butyl)-4-methoxycarbonylaniline With dmap In dichloromethane at 60℃; for 2h; | 84% |
2-(N,N-dimethylamino)ethanol
N-(n-butyl)-4-methoxycarbonylaniline
tetracaine hydrochloride
Conditions | Yield |
---|---|
Stage #1: 2-(N,N-dimethylamino)ethanol; N-(n-butyl)-4-methoxycarbonylaniline With sodium methylate at 130℃; for 8h; Stage #2: With hydrogenchloride | 83% |
isocyanic acid (3-nitro-phenyl) ester
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
In dichloromethane at 20℃; Inert atmosphere; | 80% |
2-bromo-1-cyclooctene-1-carboxylic acid
N-(n-butyl)-4-methoxycarbonylaniline
methyl 4-(2-bromo-N-butylcyclooct-1-ene-1-carboxamido)benzoate
Conditions | Yield |
---|---|
Stage #1: 2-bromo-1-cyclooctene-1-carboxylic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃; for 0.166667h; Stage #2: N-(n-butyl)-4-methoxycarbonylaniline With dmap In dichloromethane at 60℃; for 2h; | 56% |
Malonic acid monomethyl ester
N-(n-butyl)-4-methoxycarbonylaniline
N-butyl-N-(4-methoxycarbonylphenyl)-α-carbomethoxyacetamide
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane 15 min, 0 deg C then r.t., 5 h; |
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
With hydrazine hydrate for 0.5h; Heating; |
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: DMAP, DCC / CH2Cl2 / 15 min, 0 deg C then r.t., 5 h 2: MeSO2N3, DBU / acetonitrile / 0 deg C, 30 min then r.t. 3: 50 percent / 50 molpercent Nafion-H / toluene / 28 h / Heating View Scheme |
N-(n-butyl)-4-methoxycarbonylaniline
N-butyl-N-(4-methoxycarbonylphenyl)-α-carbomethoxy-α-diazoacetamide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: DMAP, DCC / CH2Cl2 / 15 min, 0 deg C then r.t., 5 h 2: MeSO2N3, DBU / acetonitrile / 0 deg C, 30 min then r.t. View Scheme |
N-(n-butyl)-4-methoxycarbonylaniline
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: DMAP, DCC / CH2Cl2 / 15 min, 0 deg C then r.t., 5 h 2: MeSO2N3, DBU / acetonitrile / 0 deg C, 30 min then r.t. 3: 10 percent / 50 molpercent Nafion-H / toluene / 28 h / Heating View Scheme |
N-(n-butyl)-4-methoxycarbonylaniline
methyl 5-butyl-4-oxo-2,3,4,5-tetrahydro-1H-cyclopenta[c]quinoline-8-carboxylate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.17 h / 20 °C 1.2: 2 h / 60 °C 2.1: palladium diacetate; caesium carbonate; tricyclohexylphosphine tetrafluoroborate / N,N-dimethyl acetamide / 4 h / 130 °C View Scheme |
N-(n-butyl)-4-methoxycarbonylaniline
methyl 5-butyl-6-oxo-5,6,7,8,9,10-hexahydrophenanthridine-2-carboxylate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.17 h / 20 °C 1.2: 2 h / 60 °C 2.1: palladium diacetate; caesium carbonate; tricyclohexylphosphine tetrafluoroborate / N,N-dimethyl acetamide / 4 h / 130 °C View Scheme |
N-(n-butyl)-4-methoxycarbonylaniline
methyl 5-butyl-6-oxo-6,7,8,9,10,11-hexahydro-5H-cyclohepta[c]quinoline-2-carboxylate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.17 h / 20 °C 1.2: 2 h / 60 °C 2.1: palladium diacetate; caesium carbonate; tricyclohexylphosphine tetrafluoroborate / N,N-dimethyl acetamide / 4 h / 130 °C View Scheme |
N-(n-butyl)-4-methoxycarbonylaniline
methyl 5-butyl-6-oxo-5,6,7,8,9,10,11,12-octahydrocycloocta[c]quinoline-2-carboxylate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.17 h / 20 °C 1.2: 2 h / 60 °C 2.1: palladium diacetate; caesium carbonate; tricyclohexylphosphine tetrafluoroborate / N,N-dimethyl acetamide / 4 h / 130 °C View Scheme |
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