As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
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inquiryWe are leading fine chemicals supplier in China with ISO certificate, Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED
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inquiry3-(4-METHOXY-1-NAPHTHOYL)PROPIONIC ACID CAS:3562-99-0 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 qu
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Hubei Yuanmeng Biological Technology Co., Ltd., which is located in Wuhan, China. We are specializing in the exportation of APIs, and plant extracts ect. Our products has been exported to America, Australia, Brazil, the Europe, Middle East and other
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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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inquiry3-(4-METHOXY-1-NAPHTHOYL)PROPIONIC ACID Basic information Product Name: 3-(4-METHOXY-1-NAPHTHOYL)PROPIONIC ACID Synonyms: 3-(4-METHOXY-1-NAPHTHOY
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inquiryLocated 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
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inquiryLower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
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succinic acid anhydride
1-Methoxynaphthalene
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
Conditions | Yield |
---|---|
With aluminum (III) chloride In dichloromethane at 33 - 37℃; for 6h; | 86.4% |
With carbon disulfide; aluminium trichloride | |
With aluminium trichloride; nitrobenzene |
4-(4-hydroxy-[1]naphthyl)-4-oxo-butyric acid
dimethyl sulfate
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
succinic acid anhydride
carbon disulfide
aluminium trichloride
1-Methoxynaphthalene
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
succinic acid anhydride
aluminium trichloride
1,1,1,2-tetrachoroethane
1-Methoxynaphthalene
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
succinic acid anhydride
aluminium trichloride
nitrobenzene
1-Methoxynaphthalene
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
succinic acid anhydride
carbon disulfide
aluminium trichloride
1-Methoxynaphthalene
A
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
Conditions | Yield |
---|---|
With diethyl ether; benzene |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: AlCl3; 1,1,2,2-tetrachloro-ethane View Scheme |
N1-(6-chloro-1,2,3,4-tetrahydroacridin-9-yl)butane-1,4-diamine
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
Conditions | Yield |
---|---|
With 4-methyl-morpholine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide In dichloromethane; ethyl acetate at 20℃; for 12h; Inert atmosphere; | 75% |
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
Conditions | Yield |
---|---|
With 4-methyl-morpholine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide In dichloromethane; ethyl acetate at 20℃; for 12h; Inert atmosphere; | 69% |
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
N-(1,2,3,4-tetrahydroacridin-9-yl)propane-1,3-diamine
Conditions | Yield |
---|---|
With 4-methyl-morpholine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide In dichloromethane; ethyl acetate at 20℃; for 12h; Inert atmosphere; | 65% |
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
9-(2-aminoethylamino)-1,2,3,4-tetrahydroacridine
Conditions | Yield |
---|---|
With 4-methyl-morpholine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide In dichloromethane-d2; ethyl acetate at 20℃; for 12h; Inert atmosphere; | 61% |
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
9-(4-aminobutylamino)-1,2,3,4-tetrahydroacridine
Conditions | Yield |
---|---|
With 4-methyl-morpholine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide In dichloromethane; ethyl acetate at 20℃; for 12h; Inert atmosphere; | 60% |
N1-(6-chloro-1,2,3,4-tetrahydroacridin-9-yl)ethane-1,2-diamine
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
Conditions | Yield |
---|---|
With 4-methyl-morpholine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide In dichloromethane; ethyl acetate at 20℃; for 12h; Inert atmosphere; | 60% |
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 20℃; Inert atmosphere; | 54% |
Conditions | Yield |
---|---|
With tert.-butylnitrite at 40℃; for 48h; Green chemistry; | 46% |
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
γ-(4-methoxy-1-naphthyl)butyric acid
Conditions | Yield |
---|---|
With hydrogenchloride; amalgamated zinc; acetic acid weiteres Reagens: Toluol; Behandeln des Reaktionsprodukts mit wss. Natronlauge und Dimethylsulfat; | |
With potassium hydroxide; hydrazine anschliessend Behandeln mit Dimethylsulfat; | |
With hydrogenchloride; mercury; zinc In toluene | |
With hydrogenchloride; zinc In toluene for 2h; Reflux; | |
With hydrogenchloride; zinc In water; toluene for 2h; Reflux; |
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
4-(4-hydroxy-[1]naphthyl)-4-oxo-butyric acid
Conditions | Yield |
---|---|
With aluminium trichloride; chlorobenzene | |
With sodium hydroxide |
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
Conditions | Yield |
---|---|
With diazomethane; diethyl ether | |
With sodium hydroxide; dimethyl sulfate |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid; xylene |
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
4,4'-dimethoxy-1,1'-binaphthyl
Conditions | Yield |
---|---|
With sodium hydroxide |
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
1-oxo-9-methoxy-1,2,3,4-tetrahydrophenanthrene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: amalgamated zinc; aqueous hydrochloric acid; acetic acid / weiteres Reagens: Toluol; Behandeln des Reaktionsprodukts mit wss. Natronlauge und Dimethylsulfat 2: SOCl2; diethyl ether; pyridine / Behandeln des Reaktionsprodukts mit SnCl4 in Benzol unter Kuehlung View Scheme | |
Multi-step reaction with 2 steps 1: N2H4; KOH / anschliessend Behandeln mit Dimethylsulfat 2: HF View Scheme | |
Multi-step reaction with 2 steps 1: Zn-Hg, aq. HCl / toluene 2: polyphosphoric acid / 110 - 120 °C View Scheme |
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
10,11-dihydro-5-methoxyphenanthro<2,1-d>isoxazole
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: N2H4; KOH / anschliessend Behandeln mit Dimethylsulfat 2: HF 3: sodium methylate; benzene 4: acetic acid; NH2OH+HCl View Scheme |
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
4-(4-hydroxy-[1]naphthyl)-butyric acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: amalgamated zinc; aqueous hydrochloric acid; acetic acid / weiteres Reagens: Toluol; Behandeln des Reaktionsprodukts mit wss. Natronlauge und Dimethylsulfat 2: aqueous hydriodic acid View Scheme |
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
2-formyl-9-methoxy-1-oxo-1,2,3,4-tetrahydrophenanthrene
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: N2H4; KOH / anschliessend Behandeln mit Dimethylsulfat 2: HF 3: sodium methylate; benzene View Scheme |
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: N2H4; KOH / anschliessend Behandeln mit Dimethylsulfat 2: HF 3: sodium methylate; benzene 4: acetic acid; NH2OH+HCl 5: sodium tert-butylate; tert-butyl alcohol View Scheme |
4-(4-methoxynaphthalen-1-yl)-4-oxobutanoic acid
(9-methoxy-1-oxo-1,2,3,4-tetrahydro-[2]phenanthryl)-glyoxylic acid methyl ester
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: amalgamated zinc; aqueous hydrochloric acid; acetic acid / weiteres Reagens: Toluol; Behandeln des Reaktionsprodukts mit wss. Natronlauge und Dimethylsulfat 2: SOCl2; diethyl ether; pyridine / Behandeln des Reaktionsprodukts mit SnCl4 in Benzol unter Kuehlung 3: sodium methylate; benzene View Scheme |
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