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
Welcome 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:90-04-0
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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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chengdu and import and export trade co., LTD., who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do res
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inquiryOur company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O
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inquiryChemical Name: O-Anisidine Synonyms: 2-Aminoanisole; Ortho-Anisidine; 2-methoxyaniline; 2-(o-tolyloxy)-anilin CAS No.: 90-04-0 Molecular Formula: C7H9NO Properties: colorless oily substance, melting point 6.6℃. Oxidation and discoloration i
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inquiryWe are leading fine chemicals supplier in China and Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED intermediat
Cas:90-04-0
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inquiryAppearance:white or light yellow crystalline powder Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for research and industrial manufacture. Transportation:By
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
Lonwin Industry group limited as a professional manufactor & exporter of chemical materials ,we totally haver more than 270 stuffs, we have been on this line for more than 9 years. Our chemical materials are exported to lot of countries and reg
Cas:90-04-0
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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
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
Cas:90-04-0
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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,
Product name: O-Anisidine CAS No.:90-04-0 Molecule Formula:C7H9NO Molecule Weight:123.15 Purity: 99.0% Package: 200kg/drum Description:Yellow oily liquid Manufacture Standards:Enterprise Standard TESTING ITEMS
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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Cas:90-04-0
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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
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Hunan chemfish Pharmaceutical co.,Ltd a comprehensive enterprise, is located in High-Tech Science Park,Changsha,Chia . Specializing in R&D, manufacture and marketing, we provide a wide range of products and the most professional services to meet the
Cas:90-04-0
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inquiryOur clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:90-04-0
Min.Order:1 Kilogram
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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
Amoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi
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Hangzhou ZeErRui Chemical Co., Ltd. located in Lingang industrial areas, our plant covers an area of 6000 square meters.ZeErRui dedicated to the development, production and marketing of chemicals. We have earned ourselves a good reputation at home an
Conditions | Yield |
---|---|
With bis(tri-ortho-tolylphosphine)palladium(0); (R)-(-)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl-di-tert-butylphosphine; ammonia; sodium t-butanolate In 1,4-dioxane at 100℃; for 12h; Inert atmosphere; | 95% |
With ammonium hydroxide In water at 20℃; for 9h; Green chemistry; | 94% |
With [N,N'-bis(5-sulfonatosalicylidene)-1,2-diaminoethane]copper disodium salt; ammonia; sodium hydroxide In water at 120℃; for 12h; sealed tube; | 90% |
Conditions | Yield |
---|---|
With borane-ammonia complex In methanol; water at 20℃; for 0.0833333h; | 99% |
With hydrogen In neat (no solvent) at 59.84℃; under 30003 Torr; for 3.5h; Autoclave; | 99.1% |
With sodium tetrahydroborate In methanol; water at 20℃; for 0.0833333h; Sealed tube; Green chemistry; | 99% |
Conditions | Yield |
---|---|
With ammonium hydroxide In water at 20℃; for 9h; Green chemistry; | 95% |
With ammonium hydroxide; caesium carbonate In acetonitrile for 7h; Reflux; Green chemistry; | 91% |
With iron(III) oxide; sodium hydroxide; copper(l) iodide; ammonia In ethanol; water at 90℃; for 16h; | 90% |
Conditions | Yield |
---|---|
With tris(dibenzylideneacetone)dipalladium (0); lithium hexamethyldisilazane; CyJohnPhos; 1,1,1-triphenylsilylamine In toluene at 100℃; for 17h; | 98% |
With bis(tri-ortho-tolylphosphine)palladium(0); (R)-(-)-1-[(S)-2-(dicyclohexylphosphino)ferrocenyl]ethyl-di-tert-butylphosphine; ammonia; sodium t-butanolate In 1,4-dioxane at 100℃; for 24h; Inert atmosphere; | 89% |
With bis[chloro(1,2,3-trihapto-allylbenzene)palladium(II)]; N-[2-(di(1-adamantyl)phosphino)phenyl]morpholine; ammonia; sodium t-butanolate In 1,4-dioxane at 20℃; for 14h; Inert atmosphere; chemoselective reaction; | 88% |
2-methoxylphenyl azide
2-methoxy-phenylamine
Conditions | Yield |
---|---|
With zinc(II) tetrahydroborate In 1,2-dimethoxyethane for 3h; Ambient temperature; | 89% |
Stage #1: 2-methoxylphenyl azide With hydrazine hydrate for 0.166667h; Inert atmosphere; Stage #2: for 12h; Irradiation; chemoselective reaction; | 87% |
With water for 5h; Inert atmosphere; UV-irradiation; Sealed tube; chemoselective reaction; | 66% |
Conditions | Yield |
---|---|
With ((+/-)-binap)Ni[P(OPh)3]2*2PhCH3; ammonia; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate In 1,4-dioxane at 120℃; for 18h; Inert atmosphere; Sealed tube; | A n/a B 70% |
With C28H30Cl5N3Pd; ammonia; lithium isopropoxide; sodium t-butanolate In 1,4-dioxane at 100℃; for 2h; Reagent/catalyst; Inert atmosphere; Schlenk technique; | A n/a B 68% |
1-(2-methoxyphenyl)ethanol
2-methoxy-phenylamine
Conditions | Yield |
---|---|
With sodium azide; trifluoroacetic acid In hexane at 40℃; for 4h; Sealed tube; | 60% |
With sodium azide; methanesulfonic acid; trifluoroacetic acid In hexane at 40℃; for 10h; | 60% |
Conditions | Yield |
---|---|
With hydrogen In ethanol at 100℃; under 22502.3 Torr; for 10h; Autoclave; |
Conditions | Yield |
---|---|
With bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]}; tert-butyl N-tosyloxycarbamate at 20℃; for 12h; chemoselective reaction; | A 37% B 37% |
With titanium; sulfuric acid; hydroxylamine In water; acetonitrile at 40℃; Electrochemical reaction; | |
With sulfuric acid; titanium(IV); hydroxylamine; acetic acid In water at 40℃; Electrochemical reaction; Inert atmosphere; |
Conditions | Yield |
---|---|
With hydrogen In water at 130℃; under 3750.38 Torr; for 10h; Molecular sieve; Autoclave; |
2-methoxy-phenylamine
Conditions | Yield |
---|---|
With trifluoroacetic acid In dichloromethane at 20℃; for 16h; Polystyrene; | 52% |
Conditions | Yield |
---|---|
With tetrabutylammomium bromide at 105℃; for 0.283333h; Reagent/catalyst; Temperature; | 93% |
3,5-dichloroiodobenzene
B
2-methoxy-phenylamine
C
2,2'-dimethoxyazobenzene
Conditions | Yield |
---|---|
With copper(l) iodide; caesium carbonate; N,N`-dimethylethylenediamine In 1,4-dioxane at 60℃; for 14h; Goldberg Reaction; Inert atmosphere; | A 25% B 30% C 26% |
Conditions | Yield |
---|---|
With formic acid; 10-mesityl-10H-phenothiazine; ascorbic acid In water; acetonitrile at 20℃; for 4h; Inert atmosphere; Irradiation; Sealed tube; | A 76% B 51% |
2,2'-dimethoxyazobenzene
2-methoxy-phenylamine
Conditions | Yield |
---|---|
With ammonium bromide; aluminium In methanol for 0.25h; sonication; | 90% |
With 4,4'-di-tert-butylbiphenyl; lithium; nickel dichloride In tetrahydrofuran at 20℃; Reduction; | 74% |
With SO2 In hydrogenchloride in the presence of I2, HI, or KI; |
formic acid o-anisidide
2-methoxy-phenylamine
Conditions | Yield |
---|---|
With water; sodium hydroxide In ethanol at 65 - 70℃; for 1h; | 96% |
With sodium hydroxide In ethanol; water at 40℃; Kinetics; |
Conditions | Yield |
---|---|
With formic acid; 10-mesityl-10H-phenothiazine; ascorbic acid In water; acetonitrile at 20℃; for 4h; Inert atmosphere; Irradiation; Sealed tube; | A 70% B 73% |
formic acid
2-Nitroanisole
A
formic acid o-anisidide
B
2-methoxy-phenylamine
Conditions | Yield |
---|---|
platinum on charcoal; sulfided; vanadia In water at 90 - 95℃; for 2.5h; | A 24.8% B 62.8% |
1,2-dimethoxyethane
methylene chloride
2-amino-phenol
2-methoxy-phenylamine
Conditions | Yield |
---|---|
With sodium methylate In methanol | 67.8% |
Conditions | Yield |
---|---|
With N-Bromosuccinimide; CYANAMID; bis-[(trifluoroacetoxy)iodo]benzene In acetonitrile at 20℃; for 1h; chemoselective reaction; | 88% |
With sodium hydroxide; hydroxylamine-O-sulfonic acid In acetonitrile at 20℃; for 16h; | 80% |
With N-Bromosuccinimide; N-methoxylamine hydrochloride; bis-[(trifluoroacetoxy)iodo]benzene In acetonitrile at 20℃; | 79% |
Conditions | Yield |
---|---|
With ethene; 5%-palladium/activated carbon; ammonium acetate; potassium carbonate In acetonitrile at 90℃; under 760.051 Torr; for 15h; Reagent/catalyst; Schlenk technique; | 84% |
With styrene; ammonium hydroxide In 1-methyl-pyrrolidin-2-one at 130℃; for 20h; Sealed tube; Inert atmosphere; | 72% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; Inert atmosphere; | 100% |
With cadmium(II) oxide at 80℃; for 0.166667h; Neat (no solvent); Microwave irradiation; | 98% |
With tris(pentafluorophenyl)borate In neat (no solvent) at 20℃; for 0.0166667h; Green chemistry; | 95% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane for 2h; | 100% |
With hydroxyapatite supported copper(I) oxide In acetonitrile at 50℃; for 0.0833333h; | 91% |
With triethylamine at 0 - 20℃; for 3h; | 90% |
2-methoxy-phenylamine
benzenesulfonyl chloride
N-(2-methoxyphenyl)benzenesulfonamide
Conditions | Yield |
---|---|
With pyridine for 12h; Ambient temperature; | 100% |
With sodium hydroxide at 20℃; for 1h; Addition; | 85% |
51% |
2-methoxy-phenylamine
2-chloro-ethanol
2-[2-hydroxyethyl-(2-methoxyphenyl)amino]ethanol
Conditions | Yield |
---|---|
With calcium carbonate In water at 110℃; for 72h; | 100% |
With potassium carbonate at 95℃; for 22h; | 98% |
With potassium carbonate | 88% |
2-methoxy-phenylamine
diethyl 2-ethoxymethylenemalonate
2-[(2-methoxyphenylamino)-methylene]-malonic acid diethyl ester
Conditions | Yield |
---|---|
In ethanol at 90℃; for 18h; | 100% |
at 130℃; | 99% |
In neat (no solvent) at 120℃; for 0.75h; | 98% |
Conditions | Yield |
---|---|
With Oxone; potassium hydroxide; disodium hydrogenphosphate; tetra(n-butyl)ammonium hydrogensulfate In dichloromethane; water; acetone at 0℃; for 0.75h; pH=7.5-8.5; | 100% |
With tert.-butylhydroperoxide; 3 A molecular sieve; zirconium(IV) tert-butoxide In dichloromethane for 2h; Ambient temperature; | 85% |
With dihydrogen peroxide; acetonitrile In aq. buffer at 20℃; for 1h; pH=11; Green chemistry; | 84% |
2-methoxy-phenylamine
trifluoroacetic anhydride
N-(2-methoxyphenyl)-2,2,2-trifluoro-acetamide
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 0 - 20℃; for 0.75h; | 100% |
With pyridine In dichloromethane at 0 - 20℃; for 72h; Inert atmosphere; | 99% |
In diethyl ether | |
Stage #1: 2-methoxy-phenylamine With pyridine In dichloromethane at 0℃; for 0.5h; Stage #2: trifluoroacetic anhydride In dichloromethane at 0 - 30℃; for 1.25h; | |
With pyridine In dichloromethane at 0 - 20℃; for 1.25h; |
2-methoxy-phenylamine
2-methoxylphenyl azide
Conditions | Yield |
---|---|
With tert.-butylnitrite; trimethylsilylazide In acetonitrile at 20℃; for 1h; Inert atmosphere; | 100% |
Stage #1: 2-methoxy-phenylamine With sulfuric acid; sodium nitrite In water; acetic acid at 0 - 5℃; for 0.166667h; Stage #2: With sodium azide In water; acetic acid at 0 - 5℃; for 3h; | 99% |
Stage #1: 2-methoxy-phenylamine With hydrogenchloride; sodium nitrite In water at 0℃; Inert atmosphere; Stage #2: With sodium azide; sodium carbonate In water at 0 - 20℃; pH=7 -Ca. 8; Inert atmosphere; | 96.9% |
2-Thiophenecarbonyl chloride
2-methoxy-phenylamine
N-(2-methoxyphenyl)-2-thiophenecarboxamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; | 100% |
In toluene |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In water; ethyl acetate at 20℃; for 6h; | 100% |
With sodium carbonate In dichloromethane Ambient temperature; | 98% |
With triethylamine In diethyl ether for 16h; Ambient temperature; | 98% |
Conditions | Yield |
---|---|
With potassium hydroxide; disodium hydrogenphosphate; tetra(n-butyl)ammonium hydrogensulfate In dichloromethane; acetone other substituted anilines; | 100% |
2-methoxy-phenylamine
3,4-dimethoxy-benzaldehyde
N-m,p-dimethoxybenzylidene-o-anisidine
Conditions | Yield |
---|---|
In toluene Heating; | 100% |
In neat (no solvent) Time; Irradiation; Green chemistry; | 72.6% |
With 5A molecular sieve In toluene for 4h; |
2-methoxy-phenylamine
propynoic acid ethyl ester
ethyl 3-<(2-methoxyphenyl)amino>acrylate
Conditions | Yield |
---|---|
In ethanol for 3h; Heating; | 100% |
2-(vinyloxy)ethyl isothiocyanate
2-methoxy-phenylamine
Conditions | Yield |
---|---|
at 38℃; | 100% |
2-methoxy-phenylamine
N-(2-methoxyphenyl)-4,5,6,7-tetrahydro-1H-benzimidazole-5-carboxamide
Conditions | Yield |
---|---|
In 1,2-dichloro-ethane for 2h; Ambient temperature; | 100% |
In 1,2-dichloro-ethane for 2h; Ambient temperature; Yield given; |
di-tert-butyl dicarbonate
2-methoxy-phenylamine
tert-butyl 2-methoxyphenylcarbamate
Conditions | Yield |
---|---|
In tetrahydrofuran Heating; | 100% |
In tetrahydrofuran Inert atmosphere; Reflux; | 100% |
In tetrahydrofuran for 17h; Ambient temperature; | 99% |
Conditions | Yield |
---|---|
With zirconium(IV) chloride at 20℃; for 0.25h; | 100% |
With niobium pentachloride In dichloromethane at 20℃; for 3h; | 91% |
cadmium(II) chloride In dichloromethane at 20℃; for 3h; | 91% |
2-methoxy-phenylamine
Conditions | Yield |
---|---|
Stage #1: trifluoromethyl dihydro-1,4-dioxin-3-carbonyl chloride With pyridine; polystyrene-bound 4-hydroxy-3-nitrobenzophenone In dichloromethane at 20℃; for 24h; Acylation; Stage #2: 2-methoxy-phenylamine With triethylamine In acetonitrile for 2.5h; Acylation; Heating; | 100% |
furfural
2-methoxy-phenylamine
N-[(furan-2-yl)methylene]-2-methoxybenzenamine
Conditions | Yield |
---|---|
In methanol at 20℃; for 24h; | 100% |
In water at 20℃; for 2h; | 58% |
In dichloromethane for 0.5h; |
bis(trichloromethyl) carbonate
2-methoxy-phenylamine
1-Isocyanato-2-methoxy-benzene
Conditions | Yield |
---|---|
With triethylamine In dichloromethane | 100% |
In dichloromethane at 20℃; for 1.5h; | |
In dichloromethane at 0℃; for 0.5h; | |
With triethylamine In 1,2-dichloro-ethane at 0 - 85℃; for 8.5h; Inert atmosphere; | |
With triethylamine In 1,2-dichloro-ethane at 0 - 85℃; for 8.5h; Inert atmosphere; |
Conditions | Yield |
---|---|
In methanol | 100% |
Conditions | Yield |
---|---|
With 1,1'-bis(diphenylphosphino)ferrocene; tris(dibenzylideneacetone)dipalladium (0); sodium t-butanolate In toluene at 110℃; for 12h; | 100% |
With palladium diacetate; sodium t-butanolate; tri tert-butylphosphoniumtetrafluoroborate In toluene at 100℃; for 24h; Schlenk technique; Inert atmosphere; | 100% |
With potassium hydroxide; copper(II) oxide In dimethyl sulfoxide at 110℃; for 1.7h; | 98% |
Conditions | Yield |
---|---|
With zirconium(IV) chloride at 20℃; for 0.25h; | 100% |
With activated-[Zr6O4(OH)4(BDC-C5H4NOS)6]*4.5H2O*3.5DMF In neat (no solvent) at 20℃; for 12h; regioselective reaction; | 95% |
With niobium pentachloride In dichloromethane at 20℃; for 1.5h; | 91% |
With tungstophosphoric acid In dichloromethane at 20℃; for 3h; | 85% |
With zirconyl triflate In acetonitrile at 20℃; for 1h; regioselective reaction; | 82% |
Conditions | Yield |
---|---|
With ammonium formate; palladium on activated charcoal In methanol; water at 20℃; for 3.5h; | 100% |
2-methoxy-phenylamine
propiononitrile
A
2-methoxy-N,N-dipropyl aniline
B
2-methoxy-N-propylaniline
Conditions | Yield |
---|---|
With ammonium formate; palladium on activated charcoal In methanol; water at 20℃; for 3.1h; | A n/a B 100% |
Conditions | Yield |
---|---|
With 4 A molecular sieve In toluene at 20℃; for 24h; Condensation; | 100% |
In dichloromethane at 20℃; for 18h; Molecular sieve; |
Conditions | Yield |
---|---|
at 20℃; for 0.133333h; Milling; Inert atmosphere; | 100% |
In methanol for 5h; Heating / reflux; | 85% |
In methanol at 5 - 20℃; |
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane at 20℃; for 12h; | 100% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 100% |
2-methoxy-phenylamine
propynoic acid ethyl ester
ethyl 3-(2-methoxyphenylamino)acrylate
Conditions | Yield |
---|---|
In ethanol | 100% |
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