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 according to the contract research and development services for the fine c
Cas:111-87-5
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inquiry1-Octanol Chemical Properties Melting point −15 °C(lit.) Boiling point 196 °C(lit.) density 0.827 g/mL at 25 °C(lit.) vapor density 4.5 (vs air) vapor pressure 0.14 mm Hg (
Cas:111-87-5
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inquiryItems Standard Result Assay (Ursolic acid) 98%min 98.22% -----------------------------------------------------------------------------------------------------------
Cas:111-87-5
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inquiryHebei Yanxi Chemical Co., Ltd. is a professional research, development and production of lead acetate benzene acetamide enterprise backbone members by local well-known entrepreneurs and professional senior engineers in the party's "low car
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
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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inquiryOur 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 advantages: 1, High quality with competitive price: 1) Standard:BP/USP/EP/Enterprise standard 2) All Purity≥99% 3) We are manufacturer and can provide high quality products with factory price. 2, Fast and safe delivery 1) Parcel can be sent
Name: 1-Octanol CAS:111-87-5 MF: C8H18O Appearance:colorless transparent liquid Storage:Preserve in well-closed, light-resistant and airtight containers. Package:25kg Application: used as spices, octanal, octanic acid and their ester raw materials
WITH 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
Cas:111-87-5
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inquiryOur Advantage: high quality with competitive price High quality standard: BP/USP/EP Enterprise standard All purity customized Fast and safe delivery We have reliable forwarder who can help us deliver our goods more fast and safe. We
Cas:111-87-5
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inquiryAbout Product Details 1-Octanol Basic information Chemical proper
Cas:111-87-5
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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
1.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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inquiryWe are the manufacturers and suppliers of API in China, and warehouse in Germany and USA of California, which can quickly and safely deliver to your address 1.High quality and competitive price. 2.Free sample for your evaluation. 3.Promptly delivery
Cas:111-87-5
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inquiryProduct Name: 1-Octanol CAS: 111-87-5 MF: C8H18O MW: 130.23 EINECS: 203-917-6 Mol File: 111-87-5.mol 1-Octanol Structure 1-Octanol Chemical Properties Melting point −15 °C(lit.) Boiling point 196 °C(lit.) den
Our 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 present
1-Octanol CAS:111-87-5 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 quality organic intermediates, s
Cas:111-87-5
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inquiryHello, 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
Minimum Order Qty. 10 Gram Supply Ability 500 Kilograms/Month Storage store in cool, dry, ventilated place 20℃ Delivery Time 3 business days after payment Payment Term TT,western union,Paypal,MoneyGram Package 10g,20g,50g,100g,500g,1KGS,
Cas:111-87-5
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inquiry1-Octanol CAS:111-87-5 Specification Density: 0.8±0.1 g/cm3 Boiling Point: 194.7±3.0 °C at 760 mmHg Vapour Pressure: 0.1±0.8 mmHg at 25°C Enthalpy of Vaporization: 50.1&
Henan 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
Appearance: white odourless crystals or powder Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Organic Chemistry Transportation:Common products:Sea/Air/Courier Da
Our Services 1. New Molecules R&D 2. Own test center HPLC NMR GC LC-MS 3. API and Intermediates from China reputed manufacturers 4. Documents support COA MOA MSDS DMF open part Our advantages 1. Government awarded company. Top 100 enter
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
Advantage 1: The product passed the professional production process and quality inspection, the purity is 99% +. 2: Highly qualified engineers to provide technical documents and service. 3: We could provide sample for your test. 4: High qualit
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
A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
Factory price 1-Octanol CAS 111-87-5 Purity: 99% Min Application: Intermediates Appearance: Powder Package: Bag Delivery: 3-5days Our Advantage & Service 1.Top quality: Using high quality material and establishing a strict quality co
Cas:111-87-5
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inquiry1-Octanol CAS 111-87-5 Our advantage 1.Top quality: Using high quality material and establishing a strict quality control system,assigning specific persons in charge of each part of production,from raw material purchase to assembly. 2 Profe
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inquiryConditions | Yield |
---|---|
With 1-Iodooctane at 146℃; | A n/a B n/a C n/a D 100% |
Conditions | Yield |
---|---|
With 1-bromo-octane at 146℃; | A n/a B n/a C n/a D 100% |
2-(octyloxy)-tetrahydrofuran
octanol
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In ethanol for 1h; Ambient temperature; | 100% |
oct-1-ene
thexylchloroborane * dimethylsulfide
A
octanol
B
rac-octan-2-ol
C
2,3-dimethylbutan-2-ol
Conditions | Yield |
---|---|
With methanol; dihydrogen peroxide Product distribution; different solvents; other olefins; | A 99.2% B 0.8% C 100% |
trimethyl(oct-1-yloxy)silane
octanol
Conditions | Yield |
---|---|
With dinitrogen tetraoxide In dichloromethane at -10℃; deprotection; | 100% |
With water; 1,1,1,3,3,3-hexamethyl-disilazane In dichloromethane at 20℃; for 0.483333h; | 100% |
With polymer-supported ammonium fluoride: D296 In methanol at 20℃; for 2h; | 98% |
Conditions | Yield |
---|---|
With hydrogen; Et4N In 1,2-dimethoxyethane at 100℃; under 38000 Torr; for 13h; | 100% |
With zirconium(IV) tetraisopropoxide 2-propanol; 4 Angstroem MS; 1,1'-bi-2-naphthol In isopropyl alcohol; toluene at 20℃; for 18h; | 100% |
With zirconium(IV) tetraisopropoxide 2-propanol; 1,1'-bi-2-naphthol In toluene at 20℃; for 1h; | 100% |
1-Chloroethyl n-Octyl Crbonate
A
octanol
B
n-octyl 1-thiocyanoethylcarbonate
Conditions | Yield |
---|---|
In methanol for 27h; Ambient temperature; | A 22% B 100% |
2-methyl-4-(octyloxy)but-2-ene
octanol
Conditions | Yield |
---|---|
With titanium tetrachloride; tetra-(n-butyl)ammonium iodide In dichloromethane at 0℃; for 2h; deprenylation; | 100% |
With 1.3-propanedithiol; cerium(III) chloride; sodium iodide In nitromethane for 10h; Heating; | 17% |
octanol
Conditions | Yield |
---|---|
With water at 100℃; for 24h; Kinetics; Reagent/catalyst; Inert atmosphere; | 100% |
With acetyl chloride In methanol at 20℃; for 2h; | 97% |
With zinc trifluoromethanesulfonate In methanol at 0 - 20℃; for 2h; chemoselective reaction; | 88% |
tert-butyl octyl ether
octanol
Conditions | Yield |
---|---|
With sodium iodide; cerium(III) chloride In acetonitrile at 70℃; for 3.5h; Kinetics; Further Variations:; Temperatures; effect of water; | 100% |
With cerium(III) chloride; sodium iodide In acetonitrile at 70℃; for 8h; | 94% |
With magnesium(II) perchlorate In dichloromethane at 40℃; for 5h; | |
With erbium(III) triflate In methanol at 100℃; for 0.75h; Microwave irradiation; |
2-octyloxy-tetrahydro-pyran
octanol
Conditions | Yield |
---|---|
With methanol; zirconium(IV) chloride at 20℃; for 4h; | 99% |
silica-supported prop-1-ylsulfonic acid In methanol | 99.7% |
With methanol at 20℃; for 0.5h; | 99% |
Conditions | Yield |
---|---|
With samarium diiodide; heptanal; samarium(III) trifluoromethanesulfonate In tetrahydrofuran; methanol; potassium hydroxide at 20℃; for 0.075h; Reduction; | 99% |
With 1,1,3,3-Tetramethyldisiloxane; copper(II) bis(trifluoromethanesulfonate) In toluene at 80℃; for 16h; sealed tube; | 91% |
With hydrogen In neat (no solvent) at 180℃; under 37503.8 Torr; for 12h; | 91% |
Conditions | Yield |
---|---|
With C32H36ClNO2P2Ru; potassium tert-butylate; hydrogen In neat (no solvent) at 120℃; under 38002.6 Torr; for 20h; Autoclave; Green chemistry; | 99% |
With [RuCl2((E)-N-(2-(diphenylphosphino)benzyl)-1-(6-((diphenylphosphino)methyl)pyridin-2-yl)methanimine)]; hydrogen; sodium ethanolate at 80℃; under 37503.8 Torr; for 12h; Autoclave; | 99% |
With lithium borohydride In tetrahydrofuran at 65℃; for 2h; | 98% |
octanol
Conditions | Yield |
---|---|
With ytterbium(III) triflate In methanol for 4h; Ambient temperature; | 99% |
1-methoxy-4-octyloxymethyl benzene
octanol
Conditions | Yield |
---|---|
With silver hexafluoroantimonate; 1,2,3-trimethoxybenzene In dichloromethane at 40℃; for 7h; | 99% |
With 4,4'-bipyridine; (phthalocyaninato)iron(II); oxygen; 2,3-dicyano-5,6-dichloro-p-benzoquinone In toluene at 80℃; under 3000.3 Torr; for 14h; Autoclave; | 90% |
Stage #1: 1-methoxy-4-octyloxymethyl benzene With sodium hydrogencarbonate; bis-[(trifluoroacetoxy)iodo]benzene; meso-2,5-bis(methoxycarbonyl)-2,5-dimethylpyrrolidine-1-oxyl In dichloromethane at 20℃; for 2h; Stage #2: With water In dichloromethane chemoselective reaction; | 90% |
2-octen-1-al
octanol
Conditions | Yield |
---|---|
With acetylacetonatodicarbonylrhodium(l); trifluorormethanesulfonic acid; carbon monoxide; N-(5-diphenylphosphanylpyrrole-2-carbonyl)guanidine; hydrogen In dichloromethane at 40℃; under 15001.5 Torr; for 7h; Autoclave; chemoselective reaction; | 99% |
Conditions | Yield |
---|---|
With oxonium; oxygen; diisobutyl(2,6-di-tert-butyl-4- methylphenoxy)aluminum Product distribution; regioselectivity of hydroalumination; | A 98% B n/a |
Stage #1: oct-1-ene With 1-bromo-butane; sodium tetrahydroborate; Aliquat 336 at 20℃; for 16h; Addition; Hydroboration; Stage #2: With sodium hydroxide; dihydrogen peroxide at 40℃; for 1h; Oxidation; | A 88% B 6% |
With sodium tetrahydroborate; oxygen; (2,3,7,8,12,13,17,18-octaethylporphyrinato)rhodium(III) chloride In tetrahydrofuran Ambient temperature; 48-130 h; Yield given; |
tert-Butyl-dimethyl-octyloxy-silane
octanol
Conditions | Yield |
---|---|
With acetyl chloride In methanol at 0 - 5℃; for 0.0833333h; | 98% |
With maleic acid In water; acetonitrile at 20℃; for 2h; | 98% |
With potassium hydrogensulfate In methanol at 20℃; for 1.5h; | 96% |
methoxymethyl octyl ether
octanol
Conditions | Yield |
---|---|
With pyridinium p-toluenesulfonate In butanone for 7.25h; Heating; | 97% |
phosphotungstic acid In ethanol for 3.5h; Heating; | 92% |
With 1-methylimidazole hydrogen sulfate at 120℃; for 0.0333333h; Microwave irradiation; chemoselective reaction; | 91% |
With bismuth(III) chloride; water In acetonitrile at 50℃; for 8h; | 84% |
(2-Methoxyethoxy)methyl octyl ether
octanol
Conditions | Yield |
---|---|
With pyridinium p-toluenesulfonate In butanone for 8.5h; Heating; | 97% |
S-sec-butyl caprylthioate
octanol
Conditions | Yield |
---|---|
With Li(1+)*C12H28AlO3(1-) In tetrahydrofuran; hexane for 0.5h; Ambient temperature; | 97% |
Conditions | Yield |
---|---|
With C30H34Cl2N2P2Ru; potassium methanolate; hydrogen In tetrahydrofuran at 100℃; under 38002.6 - 76005.1 Torr; for 15h; Reagent/catalyst; Temperature; Pressure; Glovebox; Autoclave; | 96% |
Stage #1: octanoic acid ethyl ester With C33H58FeN3PSi2; phenylsilane In toluene at 20℃; for 4h; Inert atmosphere; Glovebox; Green chemistry; Stage #2: With sodium hydroxide In toluene for 1h; Green chemistry; | 80% |
With methanol; sodium tetrahydroborate; sodium ethanolate at 40℃; | 80% |
octylmagnesium bromide
octanol
Conditions | Yield |
---|---|
With titanium(IV) isopropylate; tert.-butylhydroperoxide In diethyl ether at -78℃; for 12h; | 96% |
With 2-t-butylperoxy-1,3,2-dioxaborolane In tetrahydrofuran 1.) overnight, 2.) reflux, 3 h; | 80% |
With diethyl ether; oxygen at 0℃; |
Conditions | Yield |
---|---|
With ethanol at 90℃; under 10343.2 Torr; for 16h; Catalytic behavior; Reagent/catalyst; Inert atmosphere; | 96% |
With ytterbium(III) triflate In methanol for 30h; Ambient temperature; | 80% |
With [t-Bu2SnOH(Cl)]2 In methanol at 30℃; for 6h; Deacetylation; | 93 % Chromat. |
n-butyllithium
A
octanol
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In tetrahydrofuran; hexane at -78℃; for 0.05h; | A n/a B 95% |
Conditions | Yield |
---|---|
With Amberlyst A 26; carbonate form In benzene for 4h; Heating; | 95% |
With 3-chloro-benzenecarboperoxoic acid In dichloromethane at 20℃; for 0.0166667h; | 95% |
In N,N,N,N,N,N-hexamethylphosphoric triamide; water at 100℃; for 2.5h; | 92% |
With N,N,N,N,N,N-hexamethylphosphoric triamide; air; zinc In tetrahydrofuran | 65 % Spectr. |
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; sodium iodide In acetonitrile for 0.05h; | 95% |
With ethylmagnesium chloride; iron(II) chloride In tetrahydrofuran; m-xylene at 20℃; for 1h; | 79% |
With boron trifluoride diethyl etherate; tetra-(n-butyl)ammonium iodide In chloroform at 65℃; for 5h; | 75% |
With 1.3-propanedithiol; cerium(III) chloride; sodium iodide In nitromethane for 30h; Heating; | 83 % Chromat. |
With samarium diiodide; water; isopropylamine In tetrahydrofuran at 20℃; for 0.05h; |
Conditions | Yield |
---|---|
With potassium hydroxide; tetrafluoroboric acid; sodium hydrogencarbonate; mercury(II) oxide In 1,4-dioxane 1.) room temp., 3 h; | 95% |
In N,N,N,N,N,N-hexamethylphosphoric triamide; water at 100℃; for 5.5h; | 92% |
With Amberlyst A 26; carbonate form In benzene for 4h; Heating; | 90% |
Conditions | Yield |
---|---|
Stage #1: octyl formate With phenylsilane; C74H74Mn2N6P4 at 25℃; for 0.5h; Glovebox; Inert atmosphere; Stage #2: With sodium hydroxide In water at 25℃; for 2h; Glovebox; Inert atmosphere; | 95% |
With sodium hydroxide Ambient temperature; Yield given; |
Conditions | Yield |
---|---|
With sodium tetrahydroborate; titanium tetrachloride In 1,2-dimethoxyethane for 14h; Ambient temperature; | 95% |
With diisopropoxytitanium(III) tetrahydroborate In dichloromethane at -20℃; for 0.133333h; | 86% |
Multi-step reaction with 2 steps 1: LiAlH(i-Bu)2(n-Bu) / 0.5 h / 78 °C 2: 1.)LiAlH(i-Bu)2(n-Bu) 2.) NaBH4 / 1.) 1h, -78 deg C 2.) 1h, r.t., EtOH View Scheme | |
Multi-step reaction with 2 steps 1: LiAlH(i-Bu)2(n-Bu) / 0.5 h / 78 °C 2: LiAlH(i-Bu)2(n-Bu) / tetrahydrofuran; hexane / 6 h / -78 °C / reduction of other carbonyl compounds View Scheme |
Conditions | Yield |
---|---|
cationic dirhodium(II) complex at 50℃; for 24h; | 100% |
With Rh/AlO(OH) In toluene at 25℃; for 24h; Inert atmosphere; | 90% |
dirhodium(II) tetrakis(perfluorobutyrate) In dichloromethane for 3h; Product distribution; Ambient temperature; var. alcohols; rel. reactivities for triethylsilane alcoholysis; var. catalysts; | 86% |
Conditions | Yield |
---|---|
With diphenylselenium dichloride; triphenylphosphine In benzene for 0.333333h; Product distribution; other reagent, solvent; | 100% |
With Me2SeCl2; triphenylphosphine In chloroform for 0.333333h; | 100% |
With thionyl chloride; Triphenylphosphine oxide In neat (no solvent) at 100℃; for 5h; Mechanism; Reagent/catalyst; | 100% |
Conditions | Yield |
---|---|
With nitric acid for 12h; Ambient temperature; | 100% |
With nitric acid for 12h; Ambient temperature; | 100% |
With nitric acid; urea; europium(III) trifluoromethanesulfonate In cyclohexane at 95℃; for 12h; Schlenk technique; | 96% |
Conditions | Yield |
---|---|
With nitric acid for 0.333333h; Ambient temperature; sonication; | 100% |
With nitric acid for 0.333333h; Ambient temperature; sonication; | 100% |
With ruthenium trichloride; iodobenzene; potassium peroxomonosulfate In water; acetonitrile at 20℃; for 16h; | 100% |
Conditions | Yield |
---|---|
With carbonylhydrido[6-(di-tert-butylphosphinomethylene)-2-(N,N-diethylaminomethyl)-1,6-dihydropyridine]ruthenium(II); N-(4-chlorophenyl)formamide In 1,3,5-trimethyl-benzene at 125℃; for 48h; Reagent/catalyst; | 100% |
With sodium bromate; hydrogen bromide In tetrachloromethane at 35 - 37℃; for 2h; | 99% |
With disodium hydrogenphosphate; benzyltrimethylammonium tribromide In tetrachloromethane; water at 60℃; for 8.5h; | 99% |
Conditions | Yield |
---|---|
With magnesium(II) perchlorate at 20℃; for 0.0166667h; | 100% |
With cyclopenta-1,3-diene; dimethyl cis-but-2-ene-1,4-dioate; scandium tris(trifluoromethanesulfonate) In dichloromethane at 0℃; for 12h; | 100% |
With erbium(III) chloride at 50℃; for 1h; | 100% |
Conditions | Yield |
---|---|
Stage #1: octanol With triethylamine In dichloromethane at 25℃; Stage #2: methanesulfonyl chloride In dichloromethane at 0 - 20℃; | 100% |
With triethylamine In dichloromethane at -15℃; for 1h; Green chemistry; | 100% |
With zinc oxide-nanoparticle at 50℃; for 4h; Neat (no solvent); chemoselective reaction; | 93% |
Conditions | Yield |
---|---|
With asymmetric salen type di-Schiff base-based zinc complex supported on Fe3O4 nanoparticles at 20℃; for 0.383333h; | 100% |
With ammonium thiocyanate In dichloromethane at 0℃; for 0.166667h; | 99% |
phosphotungstic acid at 55 - 60℃; for 0.116667h; | 96% |
Conditions | Yield |
---|---|
With bis(5-norbornenyl-2-methyl) azodicarboxylate; polystyrene-supported PPh3 In tetrahydrofuran Esterification; Mitsunobu reaction; | 100% |
With toluene-4-sulfonic acid for 0.05h; Irradiation; | 97% |
With 1-(tert-butyl)-2-(chlorobenzyl) azodicarboxylate; triphenylphosphine In dichloromethane at 0 - 20℃; for 4h; Reagent/catalyst; Mitsunobu Displacement; | 97.9% |
Conditions | Yield |
---|---|
erbium(III) triflate In acetonitrile at 20℃; for 2.5h; | 100% |
With erbium(III) chloride for 1.5h; Heating; | 99% |
With triethylamine In benzene at 25 - 30℃; for 1h; |
carbon disulfide
octanol
methyl iodide
O-octyl-S-methyl dithiocarbonate
Conditions | Yield |
---|---|
Stage #1: carbon disulfide; octanol With 1H-imidazole; sodium hydride In tetrahydrofuran at 20℃; for 0.5h; Addition; Stage #2: methyl iodide In tetrahydrofuran at 20℃; for 0.5h; Methylation; Further stages.; | 100% |
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In water for 1.5h; Ambient temperature; | 95% |
Stage #1: carbon disulfide; octanol In dimethyl sulfoxide at 20℃; for 0.333333h; Stage #2: With N-benzyl-trimethylammonium hydroxide In dimethyl sulfoxide at 20℃; for 1h; Stage #3: methyl iodide In dimethyl sulfoxide at 20℃; for 2h; | 93% |
Conditions | Yield |
---|---|
With pyridinium p-toluenesulfonate In toluene for 2h; Heating; | 100% |
In toluene for 2h; Heating / reflux; | 100% |
With sulfuric acid In benzene Heating; | 87% |
Conditions | Yield |
---|---|
With Keggin-type 12-tungstophosphoric acid supported on MCM-41 at 80℃; for 1h; | 100% |
LaY zeolite at 116℃; for 6h; Acetylation; | 98% |
With bismuth(lll) trifluoromethanesulfonate at 20℃; for 0.5h; | 98% |
Conditions | Yield |
---|---|
With bis(5-norbornenyl-2-methyl) azodicarboxylate; polystyrene-supported PPh3 In tetrahydrofuran Substitution; Mitsunobu reaction; | 100% |
With 1-(tert-butyl)-2-(chlorobenzyl) azodicarboxylate; triphenylphosphine In dichloromethane at 0 - 20℃; for 5h; Reagent/catalyst; Mitsunobu Displacement; | 89.6% |
With tagged 3-(diphenylphosphino)propionic acid t-butyl ester; tagged di-t-butylazodicarboxylate Yield given; |
Conditions | Yield |
---|---|
[Cl(C6F13C2H4)2SnOSn(C2H4C6F13)2Cl]2 In various solvent(s) at 150℃; for 16h; | 100% |
With sulfonated polypyrene In n-heptane at 110℃; for 6h; | 97% |
With chloro-trimethyl-silane; diphenylammonium trifluoromethanesulfonate In toluene at 80 - 110℃; for 24h; Esterification; | 94% |
With high p-toluenesulfonate content diphenylamine and terephthalaldehyde resin In neat (no solvent) at 110℃; for 24h; | 94% |
Conditions | Yield |
---|---|
With [Cl(C6F13C2H4)2SnOSn(C2H4C6F13)2Cl]2 In various solvent(s) at 150℃; for 10h; | 100% |
With sulfonated polypyrene In n-heptane at 110℃; for 2h; | 98% |
With trifluorormethanesulfonic acid at 80℃; for 18h; Reagent/catalyst; Temperature; Sealed tube; | 98% |
Conditions | Yield |
---|---|
erbium(III) triflate In acetonitrile at 50℃; for 0.5h; | 100% |
With bismuth(lll) trifluoromethanesulfonate In acetonitrile for 0.416667h; Heating; | 97% |
Sulfate; tin(IV) oxide In acetonitrile at 20℃; for 3h; | 90% |
octanol
ethyl dihydrocinnamate
A
ethanol
B
1-octyl 3-phenylpropanoate
Conditions | Yield |
---|---|
2[{Cl(C6F13CH2CH2)2SnOSn(CH2CH2C6F13)2Cl}2] In various solvent(s) at 150℃; for 16h; | A n/a B 100% |
octanol
2,2-dimethylpropanoic anhydride
1-octyl 2,2-dimethylpropanoate
Conditions | Yield |
---|---|
erbium(III) triflate In acetonitrile at 20℃; for 0.416667h; | 100% |
With magnesium(II) perchlorate at 40℃; for 5h; | 99% |
With erbium(III) chloride at 50℃; for 2h; | 99% |
With bismuth(lll) trifluoromethanesulfonate In dichloromethane; water at 25℃; for 4h; | 98% |
Conditions | Yield |
---|---|
erbium(III) triflate In acetonitrile at 20℃; for 0.25h; | 100% |
With erbium(III) chloride at 50℃; for 1.5h; | 99% |
With magnesium(II) perchlorate at 20℃; for 0.5h; | 98% |
octanol
4-(4-Carboxy-butoxy)-benzoic acid
Conditions | Yield |
---|---|
With [Cl(C6F13C2H4)2SnOSn(C2H4C6F13)2Cl]2 In various solvent(s) at 150℃; for 16h; | 100% |
Conditions | Yield |
---|---|
Stage #1: octanol With 2,2,6,6-tetramethyl-piperidine-N-oxyl; [bis(acetoxy)iodo]benzene In dichloromethane for 16h; Stage #2: benzylamine With sodium tetrahydroborate In dichloromethane chemoselective reaction; | 100% |
With potassium carbonate; bis[dichloro(pentamethylcyclopentadienyl)iridium(III)] In toluene at 90℃; for 17h; | 88% |
With sodium hydrogencarbonate; bis[dichloro(pentamethylcyclopentadienyl)iridium(III)] In toluene at 90℃; for 17h; | 86% |
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