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Cas:88-69-7
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Cas:88-69-7
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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
Product Detail Minimum Order Qty. 10 Gram
Cas:88-69-7
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inquiryAppearance:off-white to white solid Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for Synthesis API and Research Transportation:By Sea/Air/Courier Port:Qingdao
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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:88-69-7
Min.Order:10 Gram
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inquiry2-IsopropylphenolAppearance:Pls see the Details Storage:Keep away of light, hot, water, Store in dry, dark and ventilated place Package:according to customers' requirements Application:Steroids, Cosmetics Ingredients, APIs, Intermediates, OLED&Batter
superior quality Appearance:CLEAR SLIGHTLY YELLOW LIQUID 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:2-Isopropylphenol is an impurity of Propo
CAS:88-69-7 EINECS:201-852-8 MW:136.19 MF:C9H12O Melting point:12-16 °C(lit.) Boiling point212-213 °C(lit.) Package:200kg/Steel drum Transportation:by sea Port:Shanghai
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R & D enterprises have their own stock in stockAppearance:To be subject to the object Package:Customized Application:pharmaceutical intermediates Transportation:Air Port:Shanghai;Guangzhou
high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,Pharmaceutical intermediates Transportation:air,sea,courier
Our 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:88-69-7
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
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88-69-7 2-Isopropylphenol Application:88-69-7 2-Isopropylphenol
1,we produce and sell good chemicals around the world. 2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%. 3,our staff consists of highl
88-69-7 2-IsopropylphenolAppearance:powder Storage:room tempurature Package:As required Application:medical Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By air(airport to airport) or by sea LCL/FCL for large amou
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:any port in China
2-IsopropylphenolAppearance:CLEAR SLIGHTLY YELLOW LIQUID Storage:keep in dry and ventilated place Package:aluminium bag Application:intermediates Transportation:By sea/By air
Our mission is to provide high-quality and innovative products to our customers. By offering a broad range of products, custom synthesis and personalized services, Bide can help scientists speeding up their research in the chemical and pharmaceutical
1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
Cas:88-69-7
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiry2-Isopropylphenol Basic information Product Name: 2-Isopropylphenol Synonyms: 1-Hydroxy-2-isopropylbenzene;2-(1-methylethyl)-pheno;2-(1-Methylethyl)phenol;2-(1-methylethyl)-Phenol;Isopropylphenol, ortho;o
Changzhou Extraordinary Pharmatech co., LTD. As a leading chemical manufacturer and supplier in China.DAS authentication is passed.We can provide the popular precursor chemicals, we have our own strong R & D team, have our own laboratories and fa
Conditions | Yield |
---|---|
With potassium hydroxide; tris-(dibenzylideneacetone)dipalladium(0); tert-butyl XPhos In 1,4-dioxane; water at 100℃; for 6h; | 96% |
With potassium phosphate; tri-tert-butyl phosphine; tris-(dibenzylideneacetone)dipalladium(0) In toluene at 100℃; for 20h; | 38% |
With cesiumhydroxide monohydrate; bis[(trimethylsilyl)methyl](1,5-cyclooctadiene)palladium(II); 2-((di-adamantan-1-yl)phosphaneyl)-1-(2,6-diisopropylphenyl)-1H-imidazole In tetrahydrofuran at 24℃; for 20h; Inert atmosphere; |
2-isopropylphenylboronic acid
2-(1-methylethyl)phenol
Conditions | Yield |
---|---|
With iron(III) oxide; oxygen In tetrahydrofuran Irradiation; | 90% |
With iron(III) oxide; oxygen In tetrahydrofuran at 20℃; Irradiation; | 90% |
With ozone In ethanol; water at 20 - 30℃; for 0.5h; | 90% |
methylmagnesium chloride
carbonic acid tert-butyl ester 2-formyl-phenyl ester
2-(1-methylethyl)phenol
Conditions | Yield |
---|---|
In diethyl ether at 0℃; Grignard reaction; | 86% |
Conditions | Yield |
---|---|
With N,N,N,N,N,N-hexamethylphosphoric triamide; sodium hydride; N-methylaniline In diethyl ether; xylene at 120℃; for 24h; | 80% |
With hydrogen iodide | |
With boron tribromide |
(-)-menthol
phenol
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
C
isopropoxybenzene
D
3-isopropylhydroxybenzene
Conditions | Yield |
---|---|
at 120℃; for 15h; | A 64% B 23% C 10% D 3% |
isopropyl alcohol
phenol
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
C
5-propylphenol
D
2,6-diisopropylphenol
Conditions | Yield |
---|---|
With supercritical water at 399.84℃; for 1h; Kinetics; Further Variations:; Time; | A 57.9% B 2.4% C 6.9% D 5.9% |
acetic anhydride
2-isopropylaniline
A
2-(1-methylethyl)phenol
B
2-isopropylbiphenyl
C
2-isopropyl-phenyl acetate
Conditions | Yield |
---|---|
With potassium acetate; isopentyl nitrite In benzene at 80℃; for 10h; | A 14% B 6.4% C 46% |
acetic anhydride
2-isopropylaniline
A
2-(1-methylethyl)phenol
B
2-isopropylbiphenyl
C
2-isopropyl-phenyl acetate
D
3,3-dimethyl-3H-indazole
Conditions | Yield |
---|---|
With potassium acetate; isopentyl nitrite In benzene at 80℃; for 10h; | A 14% B 6.4% C 46% D 2% |
isopropyl alcohol
phenol
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
C
2,6-diisopropylphenol
D
isopropoxybenzene
Conditions | Yield |
---|---|
With HMCM-49/MCM-41 composite at 180℃; under 760.051 Torr; for 1h; Flow reactor; | A 41.6% B 13.3% C n/a D n/a |
(-)-menthol
phenol
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
C
3-isopropylhydroxybenzene
Conditions | Yield |
---|---|
at 160℃; for 15h; | A 37% B 26% C 37% |
isopropyl alcohol
phenol
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
C
2,6-diisopropylphenol
D
2,4,6-triisopropylphenol
Conditions | Yield |
---|---|
With HMCM-49 at 180℃; under 760.051 Torr; for 1h; Flow reactor; | A 35.5% B 9.4% C n/a D n/a |
Isopropylbenzene
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
C
1-methyl-1-phenylethyl alcohol
D
3-isopropylhydroxybenzene
Conditions | Yield |
---|---|
With pyridine-2-carbaldehyde; 2-(Aminomethyl)pyridine; iron(II) trifluoromethanesulfonate acetonitrile disolvate; dihydrogen peroxide In acetonitrile at 25℃; for 1.5h; chemoselective reaction; | A 7% B n/a C 6% D n/a |
With VO(O2)(picolinato)(H2O)2 In acetonitrile at 20℃; Product distribution; Mechanism; |
isopropoxybenzene
A
2-(1-methylethyl)phenol
B
2,4-diisopropylphenol
C
2,4,6-triisopropylphenol
D
phenol
Conditions | Yield |
---|---|
Einleiten von BF3; |
2-isopropenylphenol
2-(1-methylethyl)phenol
Conditions | Yield |
---|---|
With nickel Hydrogenation; | |
With ethanol; platinum Hydrogenation; |
Conditions | Yield |
---|---|
at 200℃; |
cumenesulphonic acid
2-(1-methylethyl)phenol
Conditions | Yield |
---|---|
bei der Kalischmelze; |
Conditions | Yield |
---|---|
With aluminium trichloride anschliessendes Behandeln mit H2O; |
Conditions | Yield |
---|---|
With aluminium trichloride at 100 - 120℃; |
isopropyl alcohol
phenol
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
Conditions | Yield |
---|---|
With phosphoric acid at 95 - 130℃; | |
With iron(III) chloride at 120 - 130℃; | |
With boron trifluoride |
Conditions | Yield |
---|---|
With hydrogenchloride; sodium nitrite Diazotization; | |
With sulfuric acid; cis-nitrous acid Diazotization; |
Conditions | Yield |
---|---|
With boron trifluoride | |
With phosphoric acid at 95 - 130℃; | |
With boric acid Erhitzen des Reaktionsprodukts mit wenig H2SO4 und anschliessend mit H2O; |
Conditions | Yield |
---|---|
With magnesium phenoxide at 320℃; | |
With aluminium(III) phenoxide at 220℃; | |
at 320℃; | |
at 340℃; under 72815.3 Torr; | |
In hydrogen fluoride |
Conditions | Yield |
---|---|
With boron trifluoride; benzene at 0℃; |
Conditions | Yield |
---|---|
With hydrogenchloride; aluminium silicate-catalyst |
2,4,6-triisopropylphenol
phenol
A
2-(1-methylethyl)phenol
B
2,4-diisopropylphenol
Conditions | Yield |
---|---|
With boron trifluoride |
Conditions | Yield |
---|---|
With dihydroxodifluoroboric acid Einleiten von Propen; |
Isopropylbenzene
A
2-(1-methylethyl)phenol
B
4-Isopropylphenol
C
3-isopropylhydroxybenzene
Conditions | Yield |
---|---|
With hydrogen fluoride; boron trifluoride; dihydrogen peroxide at -60℃; for 0.5h; Product distribution; | A 48 % Chromat. B 40 % Chromat. C 12 % Chromat. |
With C27H19N3O7OsS; dihydrogen peroxide; acetic acid In dichloromethane at 23℃; for 0.416667h; Catalytic behavior; Inert atmosphere; Overall yield = 84 %; | |
With [(smifH)2Fe](OTf)2; dihydrogen peroxide In water; acetonitrile at 25℃; for 1.5h; Reagent/catalyst; | A 8.1 %Chromat. B n/a C n/a |
2-(1-methylethyl)phenol
4-bromo-2-isopropyl-phenol
Conditions | Yield |
---|---|
With sodium hydroxide; bromine In dichloromethane at 15 - 20℃; for 0.75h; | 100% |
With N-Bromosuccinimide In acetonitrile at 0 - 20℃; for 4h; | 100% |
With bromine In dichloromethane at 15 - 20℃; for 0.75h; | 100% |
Conditions | Yield |
---|---|
Stage #1: 2-(1-methylethyl)phenol With sodium hydride In hexane; N,N-dimethyl-formamide at 0 - 20℃; Inert atmosphere; Stage #2: methyl iodide In hexane; N,N-dimethyl-formamide at 0 - 20℃; Inert atmosphere; | 100% |
Stage #1: 2-(1-methylethyl)phenol With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.333333h; Inert atmosphere; Stage #2: methyl iodide In N,N-dimethyl-formamide at 20℃; Inert atmosphere; | 99% |
With potassium hydroxide; tetra(n-butyl)ammonium hydrogen sulfate; triethylamine In dichloromethane; cyclohexane; water | 94% |
2-(1-methylethyl)phenol
4-bromo-2-isopropyl-phenol
Conditions | Yield |
---|---|
With hydrogenchloride; sodium sulfite In diethyl ether; chloroform | 100% |
2-(1-methylethyl)phenol
chloromethyl methyl ether
1-isopropyl-2-(methoxymethoxy)benzene
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran at 65℃; for 2.5h; | 99% |
With sodium hydride In tetrahydrofuran at 65℃; for 2.5h; Alkylation; | 99% |
With sodium hydride In tetrahydrofuran at 6.5℃; for 2.5h; Methylation; | 99% |
2-(1-methylethyl)phenol
N,N-Dimethylcarbamoyl chloride
2-isopropylphenyl dimethylcarbamate
Conditions | Yield |
---|---|
Stage #1: 2-(1-methylethyl)phenol With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; Inert atmosphere; Stage #2: N,N-Dimethylcarbamoyl chloride In N,N-dimethyl-formamide; mineral oil at 0 - 20℃; for 3h; Inert atmosphere; | 99% |
2-(1-methylethyl)phenol
trifluoromethylsulfonic anhydride
2-isopropylphenyl trifluoromethanesulfonate
Conditions | Yield |
---|---|
With pyridine In dichloromethane at -78 - 20℃; for 16h; | 99% |
With triethylamine In dichloromethane at -78 - 20℃; for 14h; Inert atmosphere; | 90% |
With triethylamine In dichloromethane at -78℃; for 14h; Inert atmosphere; | 81% |
Conditions | Yield |
---|---|
With rhodium(III) chloride; 1,3-bis-(diphenylphosphino)propane; sodium carbonate; sodium bromide In 1,4-dioxane at 120℃; under 750.075 Torr; for 24h; Inert atmosphere; chemoselective reaction; | 99% |
Conditions | Yield |
---|---|
With dmap In dichloromethane at 20℃; for 2h; | 98.3% |
With sulfuric acid at 20℃; for 0.5h; |
2-(1-methylethyl)phenol
E-styryl iodide
2-isopropylphenyl (E)-styryl ether
Conditions | Yield |
---|---|
Stage #1: 2-(1-methylethyl)phenol With copper(l) iodide; 2-(2'-pyridyl)benzimidazole; caesium carbonate In N,N-dimethyl-formamide at 20℃; for 0.0833333h; Inert atmosphere; Stage #2: E-styryl iodide In N,N-dimethyl-formamide at 90℃; for 7h; Inert atmosphere; stereospecific reaction; | 98% |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile for 29h; Reflux; | 98% |
2-(1-methylethyl)phenol
1-bromo-3-isopropyl-2-hydroxybenzene
Conditions | Yield |
---|---|
With N-Bromosuccinimide; diisopropylamine In dichloromethane for 16h; Reflux; Inert atmosphere; | 97% |
With N-Bromosuccinimide; diisopropylamine In dichloromethane for 16h; Inert atmosphere; Reflux; | 96% |
With N-Bromosuccinimide; diisopropylamine In dichloromethane at 0 - 20℃; for 2h; | 95% |
2-(1-methylethyl)phenol
5-chloropyrazine-2,3-dicarbonitrile
5-(2-isopropylphenoxy)pyrazine-2,3-dicarbonitrile
Conditions | Yield |
---|---|
With triethylamine In acetone at 20℃; for 2h; | 97% |
phthalic anhydride
2-(1-methylethyl)phenol
3,3-bis(4-hydroxy-3-isopropilphenyl)isobenzofuran-1(3H)-one
Conditions | Yield |
---|---|
With PPA; zinc(II) chloride at 100℃; for 3h; Product distribution / selectivity; | 96% |
With niobium pentachloride In methanesulfonic acid at 90℃; for 1.33333h; Friedel-Crafts Acylation; | 92% |
With Lewis acid at 90℃; for 5h; Product distribution / selectivity; | 83% |
With methanesulfonic acid at 90℃; for 5h; | 83% |
2-(1-methylethyl)phenol
(1S,4R,4aS,8R,8aS,10R)-8,10-difluoro-8,10-diisopropyl-4,4a,8,8a-tetrahydro-1,4-ethanonaphthalene-7,9(1H)-dione
Conditions | Yield |
---|---|
With (Ra)-4-hydroxy-2,6-bis(2,4,6-tricyclohexylphenyl)dinaphtho-[1,3,2]dioxaphosphepine 4-oxide; sodium carbonate; Selectfluor In toluene at 20℃; for 48h; | 96% |
With (S)-3,3'-bis-(2,4,4-tricyclohexylphenyl)-[1,1']-binaphthalenyl-2,2'-dioxaphosphoric acid; sodium carbonate; Selectfluor In toluene at 20℃; for 48h; | 96% |
bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]
2-(1-methylethyl)phenol
silver trifluoromethanesulfonate
Conditions | Yield |
---|---|
Stage #1: bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; silver trifluoromethanesulfonate In acetone at 20℃; for 0.333333h; Schlenk technique; Stage #2: 2-(1-methylethyl)phenol In acetone at 20℃; for 3h; Schlenk technique; Stage #3: With caesium carbonate In acetone at 20℃; for 2h; Schlenk technique; | 96% |
2-(1-methylethyl)phenol
1-chloro-2-butene
1-[(E)-but-2-enoxy]-2-isopropylbenzene
Conditions | Yield |
---|---|
With sodium hydroxide In N,N-dimethyl-formamide at 10 - 15℃; for 5h; | 95.08% |
With sodium hydroxide In N,N-dimethyl-formamide at 10 - 15℃; for 5h; Inert atmosphere; Industrial scale; | 95.08% |
Conditions | Yield |
---|---|
In hexane; toluene at 0 - 20℃; | 95% |
2-(1-methylethyl)phenol
ethyl (Z)-3-iodopropenoate
(Z)-3-(2-isopropyl-phenoxy)-acrylic acid ethyl ester
Conditions | Yield |
---|---|
Stage #1: 2-(1-methylethyl)phenol With copper(l) iodide; 2-(2'-pyridyl)benzimidazole; caesium carbonate In N,N-dimethyl-formamide at 20℃; for 0.0833333h; Inert atmosphere; Stage #2: ethyl (Z)-3-iodopropenoate In N,N-dimethyl-formamide at 40℃; for 0.5h; Inert atmosphere; stereospecific reaction; | 95% |
With copper(l) iodide; 2-(2'-pyridyl)benzimidazole; caesium carbonate In N,N-dimethyl-formamide at 40℃; for 2h; Inert atmosphere; | 95% |
With 1,4-diaza-bicyclo[2.2.2]octane In N,N-dimethyl-formamide at 20℃; for 3h; Inert atmosphere; stereospecific reaction; | 95% |
2-(1-methylethyl)phenol
ethyl (Z)-3-iodopropenoate
(E)-ethyl 3-(2-isopropylphenoxy)acrylate
Conditions | Yield |
---|---|
With copper(l) iodide; 2-(2'-pyridyl)benzimidazole; caesium carbonate In N,N-dimethyl-formamide at 40℃; for 0.5h; Inert atmosphere; stereospecific reaction; | 95% |
Conditions | Yield |
---|---|
With hafnium tetrakis(trifluoromethanesulfonate) In dichloromethane at 20℃; for 0.0833333h; | 95% |
Conditions | Yield |
---|---|
Stage #1: formaldehyd With triethylamine; magnesium chloride In tetrahydrofuran at 20℃; for 0.5h; Inert atmosphere; Stage #2: 2-(1-methylethyl)phenol In tetrahydrofuran at 20℃; for 4.33h; Reflux; Stage #3: With hydrogenchloride In tetrahydrofuran; diethyl ether; water at 20℃; | 94.3% |
Stage #1: 2-(1-methylethyl)phenol With methylmagnesium bromide In tetrahydrofuran; diethyl ether at 0 - 20℃; for 1.08333h; Stage #2: formaldehyd With triethylamine In tetrahydrofuran; diethyl ether; toluene at 80℃; for 4h; Further stages.; | 92% |
Stage #1: formaldehyd With triethylamine; magnesium chloride In tetrahydrofuran at 20℃; Stage #2: 2-(1-methylethyl)phenol In tetrahydrofuran for 2h; Reflux; | 85.2% |
2-(1-methylethyl)phenol
2,5-Diiodo-6-isopropylphenol
Conditions | Yield |
---|---|
With iodine; ethylamine; potassium iodide In ethanol; water at 0℃; for 0.5h; | 94% |
With sodium hypochlorite; sodium iodide; sodium hydroxide In methanol at 20℃; for 0.5h; | 78% |
Conditions | Yield |
---|---|
With sodium hydroxide In water at 90℃; for 4h; | 93% |
With sodium hydroxide In water at 90℃; for 4h; | 93% |
With sodium hydroxide for 2h; Heating; | 87% |
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 20 - 25℃; for 4h; Inert atmosphere; | 93% |
Conditions | Yield |
---|---|
With methanesulfonic acid In 1,2-dichloro-ethane for 0.5h; Heating; | 92% |
Conditions | Yield |
---|---|
With palladium diacetate; potassium phosphate; johnphos In toluene at 100℃; for 24h; | 92% |
2-(1-methylethyl)phenol
dimethyl sulfate
1-bromo-3-isopropyl-2-methoxybenzene
Conditions | Yield |
---|---|
With lithium hydroxide; benzyltri(n-butyl)ammonium chloride In dichloromethane at 20℃; for 12h; | 92% |
2-(1-methylethyl)phenol
1,7-dichloro-4-methylheptan-4-ol
C17H26Cl2O
Conditions | Yield |
---|---|
With aluminum (III) chloride Friedel Crafts alkylation; Inert atmosphere; | 92% |
Conditions | Yield |
---|---|
Stage #1: 2-(1-methylethyl)phenol With N-Bromosuccinimide; methanesulfonic acid In acetonitrile at -10 - 0℃; Inert atmosphere; Large scale; Stage #2: 1,4-diaza-bicyclo[2.2.2]octane In n-heptane at 50℃; Inert atmosphere; Large scale; | 92% |