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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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
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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
Our Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con
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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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Hello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
Cas:1806-26-4
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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
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
superior quality moderate price & quick delivery Appearance:white crystals or powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:A weak
4-N-OCTYLPHENOL Basic information Product Name: 4-N-OCTYLPHENOL Synonyms: P-N-OCTYL PHENOL;POP;4-OCTYLPHENOL;4-N-OCTYLPHENOL;1-(p-Hydroxyphenyl)octane;4-octyl-pheno;Phenol, 4-octyl-;Phenol, p-octyl- CAS: 1806-26-4 MF: C14H22O MW: 206.
factory?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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inquiryHangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu
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inquiryShandong 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
Cas:1806-26-4
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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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inquiryWe are a Union of chemistry in China, consists of chemists,engineers, laboratories,factories in China. We organize surplus capacity of R&D and production as well as custom synthesis for chemical products and chemical business project. We are supp
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inquiryStock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
Cas:1806-26-4
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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
high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,Pharmaceutical intermediates Transportation:air,sea,courier
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high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:Beijing or Guangzhou
bulk productiongoods in stockswe have the best competitive price in the marketmeantime,we are committed to service to our every customer Chemsigma International Co.,Ltd. is a chemical manufacturer, specialize in custom synthesis and organic chemical
Ansciep 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
4-Octylphenol CAS NO.1806-26-4 Application:4-Octylphenol CAS NO.1806-26-4
Appearance:solid or liquid Storage:sealed in cool and dry place Package:As customer's requested Application:Pharma Intermediate Transportation:by courier/air/sea Port:Any port in China
We are committed to providing our customers with the best products and services at the most competitive prices.Appearance:clear liquid Storage:Room temperature with sealed well Package:according to the clients requirement Application:Use as primary a
Conditions | Yield |
---|---|
With hydrogenchloride; mercury; zinc | 78% |
With hydrogenchloride; mercury; zinc | 70% |
With hydrogenchloride; amalgamated zinc; acetic acid |
Conditions | Yield |
---|---|
With bis(triphenylphosphine)nickel(II) chloride; magnesium(II) acetate tetrahydrate; 4,4'-di-tert-butyl-2,2'-bipyridine In N,N-dimethyl acetamide at 40℃; for 3h; Schlenk technique; Inert atmosphere; regioselective reaction; | 53% |
1-(4-methoxyphenyl)octan-1-one
p-Octylphenol
Conditions | Yield |
---|---|
With potassium hydroxide; hydrazine hydrate; phenol weiteres Reagens: Diaethylenglykol. Erhitzen des Reaktionsprodukts mit wss. HI, Essigsaeure und Acetanhydrid; |
Conditions | Yield |
---|---|
With hydrogen iodide; acetic acid |
Octanal
phenol
A
1,1-bis(4-hydroxyphenyl)octane
B
2-octylphenol
C
p-Octylphenol
Conditions | Yield |
---|---|
With Al3+-exchanged montmorillonite at 100℃; for 48h; Product distribution; Mechanism; other aldehydes and ketones; also AlCl3; |
Conditions | Yield |
---|---|
In water at 25℃; for 7h; Irradiation; Yields of byproduct given. Title compound not separated from byproducts; |
Octanal
phenol
A
1,1-bis(4-hydroxyphenyl)octane
B
2-octylphenol
C
p-Octylphenol
Conditions | Yield |
---|---|
With Al(3+)-montmorillonite at 100℃; for 48h; Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts; |
Octanal
phenol
A
1,1-bis(4-hydroxyphenyl)octane
B
p-Octylphenol
Conditions | Yield |
---|---|
With Al(3+)-montmorillonite at 100℃; for 48h; Yield given. Further byproducts given. Yields of byproduct given; | |
With Al(3+)-montmorillonite at 100℃; for 48h; Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts; |
Conditions | Yield |
---|---|
With sodium hydroxide; cetyltrimethylammonim bromide In water at 25℃; Kinetics; |
4-octylaniline
p-Octylphenol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) NaNO2, 3M aq. HCl, 2.) NaOAc, Na2SO3 / 1.) H2O, 0 deg C, 20 min, 2.) H2O, 0 deg C, 16 h 2: H2O / 7 h / 25 °C / Irradiation View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: AlCl3 / nitrobenzene / 0.5 h / 50 °C 2: Zn-Hg, 5 N HCl / ethanol / Heating View Scheme | |
Multi-step reaction with 2 steps 1: 57 percent / AlCl3 / nitrobenzene / 8 h / Ambient temperature 2: 78 percent / Zn(Hg), HCl View Scheme | |
Multi-step reaction with 2 steps 1: AlCl3 / CH2Cl2 / 1.) 0 deg C, 30 min; 0 deg C, 30 min; 2.) room temperature, overnight 2: 1.) hydrazine hydrate, 2.) KOH / 1.) diethylene glycol, reflux, 1h; 2.) reflux, 1h View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: AlCl3 / nitrobenzene / 0.5 h / 50 °C 2: Zn-Hg, 5 N HCl / ethanol / Heating View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 86 percent / SOCl2 2: 60 percent / AlCl3 / nitrobenzene 3: 70 percent / Zn(Hg), HCl View Scheme | |
Multi-step reaction with 5 steps 1: thionyl chloride / 60 °C / Reflux 2: 70 - 75 °C 3: aluminum (III) chloride / 3.5 h / 20 - 100 °C 4: hydrazine hydrate / diethylene glycol / 2 h / Reflux 5: potassium hydroxide / diethylene glycol / 5 h / 20 - 200 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 60 percent / AlCl3 / nitrobenzene 2: 70 percent / Zn(Hg), HCl View Scheme | |
Multi-step reaction with 3 steps 1: aluminum (III) chloride / 3.5 h / 20 - 100 °C 2: hydrazine hydrate / diethylene glycol / 2 h / Reflux 3: potassium hydroxide / diethylene glycol / 5 h / 20 - 200 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 86 percent / SOCl2 2: 60 percent / AlCl3 / nitrobenzene 3: 70 percent / Zn(Hg), HCl View Scheme | |
Multi-step reaction with 2 steps 1: 57 percent / AlCl3 / nitrobenzene / 8 h / Ambient temperature 2: 78 percent / Zn(Hg), HCl View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: AlCl3 / CH2Cl2 / 1.) 0 deg C, 30 min; 0 deg C, 30 min; 2.) room temperature, overnight 2: 1.) hydrazine hydrate, 2.) KOH / 1.) diethylene glycol, reflux, 1h; 2.) reflux, 1h View Scheme | |
Multi-step reaction with 2 steps 1: AlCl3 / 100 - 130 °C 2: amalgamated zinc; concentrated aqueous HCl; glacial acetic acid View Scheme | |
Multi-step reaction with 2 steps 1: AlCl3 / 100 - 130 °C 2: amalgamated zinc; concentrated aqueous HCl; glacial acetic acid View Scheme | |
Multi-step reaction with 2 steps 1: zuletzt bei 100grad, und Erwaermen des Reaktionsprodukts mit AlCl3 in Nitrobenzol auf 75grad 2: amalgamated zinc; diluted aqueous HCl / 100 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1,1,2,2-tetrachloro-ethane; AlCl3 2: N2H4+H2O; KOH; phenol / weiteres Reagens: Diaethylenglykol. Erhitzen des Reaktionsprodukts mit wss. HI, Essigsaeure und Acetanhydrid View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: HI, AcOH View Scheme |
C14H22N2O
p-Octylphenol
Conditions | Yield |
---|---|
With potassium hydroxide In diethylene glycol at 20 - 200℃; for 5h; |
oct-1-ene
phenol
A
octyloxybenzene
B
2-octylphenol
C
p-Octylphenol
Conditions | Yield |
---|---|
With porous aromatic framework modified by aluminum chloride at 90℃; for 6h; Reagent/catalyst; Temperature; Friedel-Crafts Alkylation; Autoclave; |
p-Octylphenol
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen; acetic acid at 80℃; under 7500.75 Torr; for 2h; Pressure; Reagent/catalyst; Autoclave; |
4-bromoethylbutanoate
p-Octylphenol
4-(4-octylphenoxy)butyric acid ethyl ester
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In acetone for 18h; Reflux; | 100% |
With potassium carbonate In acetone Reflux; | 71% |
With potassium carbonate In acetone for 24h; Heating / reflux; | 71% |
Conditions | Yield |
---|---|
With potassium hydroxide; tetrabutylammomium bromide at 20℃; for 5h; | 99% |
Conditions | Yield |
---|---|
Stage #1: p-Octylphenol With pyridine In dichloromethane at -10℃; for 0.0833333h; Inert atmosphere; Stage #2: trifluoromethanesulfonic anhydride In dichloromethane Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 5h; Reflux; | 98% |
With potassium carbonate In acetone for 5h; Reflux; | 98% |
p-Octylphenol
N,N-Dimethylthiocarbamoyl chloride
O-p-octylphenyl N,N-dimethylthiocarbamate
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide at 85℃; | 93% |
p-Octylphenol
2-cyanoethyl-N,N-(diisopropylamino)chlorophosphine
C23H39N2O2P
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane for 0.5h; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
In ethanol; water for 48h; Reflux; | 90% |
p-Octylphenol
2-iodo-4-octylphenol
Conditions | Yield |
---|---|
With iodine; silver trifluoroacetate In dichloromethane at 0 - 20℃; | 87% |
With iodine; silver trifluoroacetate at 0 - 20℃; for 1h; | 87% |
1-oxiranylmethylindole-5-carbonitrile
p-Octylphenol
1-[2-hydroxy-3-(4-octylphenoxy)propyl]indole-5-carbonitrile
Conditions | Yield |
---|---|
With dmap In dichloromethane at 60℃; for 2h; | 85% |
Conditions | Yield |
---|---|
85% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere; Sealed tube; | 85% |
p-Octylphenol
(S)-oxiranemethanol
(R)-2-(4-octylphenoxymethyl)oxirane
Conditions | Yield |
---|---|
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃; for 24h; Mitsunobu reaction; | 84% |
p-Octylphenol
2-chloro-1-methyl-benzimidazole
1-Methyl-2-(4-octyl-phenoxy)-1H-benzoimidazole
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide for 24h; Heating; | 83% |
p-Octylphenol
2-Nitro-4-octyl-phenol
Conditions | Yield |
---|---|
With nitric acid; acetic acid In chloroform for 1.5h; Ambient temperature; | 82% |
With NaNO3; sulfuric acid In hexane; water; ethyl acetate | 68% |
With nitric acid; acetic acid |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 1h; | 81% |
di-tert-butyl 5-(oxiran-2-ylmethoxy)indole-1,2-carboxylate
p-Octylphenol
di-tert-butyl 5-[2-hydroxy-3-(4-octylphenoxy)propoxy]indole-1,2-carboxylate
Conditions | Yield |
---|---|
With dmap at 40℃; for 48h; | 81% |
p-Octylphenol
(R)-tert-butyl 2,2-dimethyl-4-[(tosyloxy)methyl]-oxazolidine-3-carboxylate
(S)-tert-butyl 2,2-dimethyl-4-[(4-octylphenoxy)methyl]oxazolidine-3-carboxylate
Conditions | Yield |
---|---|
Stage #1: p-Octylphenol With sodium hydride In N,N-dimethyl-formamide; mineral oil at 20℃; for 0.5h; Stage #2: (R)-tert-butyl 2,2-dimethyl-4-[(tosyloxy)methyl]-oxazolidine-3-carboxylate In N,N-dimethyl-formamide; mineral oil at 70℃; for 3h; | 81% |
p-Octylphenol
2-bromo-4-octylphenol
Conditions | Yield |
---|---|
With bromine; sodium hydrogencarbonate In chloroform at 0℃; | 80% |
With bromine; 1,2-dichloro-ethane |
p-Octylphenol
(R)-oxiranemethanol
(S)-2-(4-octylphenoxymethyl)oxirane
Conditions | Yield |
---|---|
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃; for 24h; Mitsunobu reaction; | 80% |
Conditions | Yield |
---|---|
In toluene at 110℃; for 20h; | 78% |
3-[2-(4-benzyloxyphenyl)-5-methyl-1H-pyrrol-1-yl]propan-1-ol
p-Octylphenol
1,1'-(Azodicarbonyl)dipiperidin
2-(4-benzyloxyphenyl)-5-methyl-1-[3-(4-octyloxyphenyl)propyl]-1H-pyrrole
Conditions | Yield |
---|---|
With triphenylphosphine In toluene | 77.4% |
p-Octylphenol
chloromethyl methyl ether
1-methoxymethoxy-4-octyl-benzene
Conditions | Yield |
---|---|
With sodium hydroxide; Aliquat 336 In dichloromethane; water at -10℃; for 0.5h; | 74% |
p-Octylphenol
C21H23BrF4O
(Z)-4-(hexyloxy)-4'-(2,3,3-trifluoro-3-(4-octylphenoxy)prop-1-enyl)biphenyl
Conditions | Yield |
---|---|
With potassium carbonate In dimethyl sulfoxide at 80℃; Schlenk technique; Inert atmosphere; stereoselective reaction; | 74% |
1,3-dibromo-2,2-dimethoxypropane
p-Octylphenol
Conditions | Yield |
---|---|
With 18-crown-6 ether; potassium carbonate In N,N-dimethyl-formamide for 10h; Reflux; | 74% |
p-Octylphenol
tert-butyl 1-(oxiran-2-ylmethyl)indazole-5-carboxylate
tert-butyl 1-[2-hydroxy-3-(4-octylphenoxy)propyl]indazole-5-carboxylate
Conditions | Yield |
---|---|
With dmap at 120℃; for 2h; | 73% |
Conditions | Yield |
---|---|
With hydrogen bromide; acetic acid for 0.333333h; | 71% |
p-Octylphenol
3-(triethoxypropyl) isocyanate
4-octylphenyl-3-(triethoxysilyl)propylcarbamate
Conditions | Yield |
---|---|
With DBDU In tetrahydrofuran at 75℃; for 24h; | 71% |
Conditions | Yield |
---|---|
With potassium carbonate; formamide In 1,4-dioxane at 95℃; for 24h; | 70% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 40℃; | 70% |