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
Cas:139-02-6
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
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Cas:139-02-6
Min.Order:1 Kilogram
FOB Price: $1000.0
Type:Lab/Research institutions
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Cas:139-02-6
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquirysuperior quality Appearance:white to reddish colored solid 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:Used as an antiseptic and in organic sy
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
Cas:139-02-6
Min.Order:0 Metric Ton
Negotiable
Type:Lab/Research institutions
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Cas:139-02-6
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
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Cas:139-02-6
Min.Order:1 Kilogram
FOB Price: $5.0
Type:Lab/Research institutions
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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
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:139-02-6
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryhigh 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
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Product name: sodium phenol English synonyms: phenol sodium salt; Sodium benzene oxidation; Sodium phenol; Sodium benzene; Sodium phenol; Carbolic acid sodium; Sodium benzene oxygen; Phenol sodium, 98% English name: Sodium benzenolate English
ProductName: Normal 0 false false f…Appearance:white to pale cream powder Package:250 / 500 / 1000 gm / 1 Kg Transportation:FOB/CIF/DDU
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Styrenated Phenol 1. Styrenated Phenol 4010NA (IPPD) 2. excellent non-polluting antioxidant 3. used in rubber products Styrenat…
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ProName: Sodium benzenolate CasNo: 139-02-6 Appearance: white to pale cream powder Application: It is an important raw material and in... DeliveryTime: prompt PackAge: according to the clients requirement
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Conditions | Yield |
---|---|
With water; sodium hydroxide In dimethyl sulfoxide at 25℃; Kinetics; | A 100% B n/a |
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water | 98.9% |
With sodium In 1,4-dioxane for 4h; Heating; | 92% |
With methanol; sodium |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 100℃; for 24h; | 65% |
Conditions | Yield |
---|---|
With oxygen; bismuth(III) nitrate; palladium on activated charcoal In sodium hydroxide at 90℃; for 6h; Product distribution; also with coactivator and other activators, various times, reaction with other 2-phenoxyethanols; | A n/a B 53% |
methanol
dimethyl phenyl phosphate
sodium methylate
A
trimethyl phosphite
B
sodium phenoxide
Conditions | Yield |
---|---|
at 0℃; Rate constant; | |
at 19℃; Rate constant; | |
at 10℃; Rate constant; |
diethyl ether
ethanol
trichloro-methanesulfenic acid phenyl ester
sodium ethanolate
A
trichloro-methanesulfenic acid ethyl ester
B
sodium phenoxide
ethanol
diphenyldiphenoxysilane
A
1,1,3,3,5,5-hexaphenylcyclotrisiloxane
B
sodium phenoxide
1,3,5-trinitro-2,4,6-triphenoxy-benzene
sodium ethanolate
A
1,3,5-triethoxy-2,4,6-trinitrobenzene
B
sodium phenoxide
diphenyldiphenoxysilane
acetone
A
1,1,3,3,5,5-hexaphenylcyclotrisiloxane
B
sodium phenoxide
Conditions | Yield |
---|---|
at 310 - 360℃; Rate constant; |
N,N'-bis(diphenyloxyphosphonyl)-8-quinolinesulfinamidine
A
sodium phenoxide
B
sodium naphthalene-1-sulfinate
Conditions | Yield |
---|---|
With sodium hydroxide for 3h; Product distribution; Heating; |
Conditions | Yield |
---|---|
With sodium hydroxide In 1,4-dioxane; water at 15℃; Rate constant; Thermodynamic data; Kinetics; var. temperatures, var. ratio of solvents, log A, Ea; |
phenoxy radical
sodium phenoxide
Conditions | Yield |
---|---|
With Sodium borate; sodium azide; oxygen; sodium formate In water Rate constant; Irradiation; combination with superoxid anion radicals; |
phenyl N-methyl-N-m-nitrophenylcarbamate
A
N-methyl-3-nitroaniline
B
sodium phenoxide
Conditions | Yield |
---|---|
With sodium hydroxide; cetyltrimethylammonim bromide In methanol; water at 68.5℃; Rate constant; Mechanism; other N-methyl-N-arylcarbamates; reaction in absence of cetyltrimethylammonium bromide; |
Methyl-(4-nitro-phenyl)-carbamic acid phenyl ester
A
sodium phenoxide
B
N-methyl(p-nitroaniline)
Conditions | Yield |
---|---|
With sodium hydroxide; cetyltrimethylammonim bromide In methanol; water at 68.5℃; Rate constant; |
Conditions | Yield |
---|---|
With sodium cation In water; dimethyl sulfoxide at 25℃; Equilibrium constant; |
Conditions | Yield |
---|---|
With sodium tetrahydroborate; hydrogen; PdCl2 complex on modified silca gel In methanol at 20℃; under 760 Torr; Rate constant; hydrogenolysis of chlorobenzenes in the presence of palladium chloride complex deposited on modified silica gel; effect of the nature of substituents in aromatic ring; |
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water at 25℃; Rate constant; Mechanism; Thermodynamic data; enegy parameters calculated from kobs in range 25-60 deg C; pH range 12.7, 13.9; |
N',N'-Dimethyl-hydrazinecarboxylic acid phenyl ester
A
sodium phenoxide
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water at 25℃; Rate constant; Mechanism; Thermodynamic data; energy parameters calculated from kobs in range 25-60 deg C; pH range 12.0, 14.9; |
A
sodium phenoxide
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water at 25℃; Rate constant; Mechanism; Thermodynamic data; energy parameters calculated from kobs in range 25-60 deg C; pH range 13.0, 13.9; |
A
sodium phenoxide
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water at 25℃; Rate constant; Mechanism; Thermodynamic data; energy parameters calculated from kobs in range 25-60 deg C; pH range 13.6, 14.1; |
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water at 25℃; Rate constant; Thermodynamic data; Mechanism; energy parameters calculated from kobs in range 25-60 deg C; pH range 11.9, 14.9; |
Conditions | Yield |
---|---|
at 250 - 260℃; |
Conditions | Yield |
---|---|
at 35℃; Product distribution; | |
at 75℃; Product distribution; |
Conditions | Yield |
---|---|
poly<1-hydroxyethylene-co-1-(2-ethylsulf In 1,4-dioxane at 75℃; for 23h; Product distribution; Rate constant; other catalysts; | 100% |
Sucrose-ethyleneoxide adducts In toluene at 110℃; for 8h; Product distribution; further catalysts: PEG, DB18K6; further objects of study: phase-transfer catalysis; | 100% |
dodecyldimethylsulfonium methyl sulfate In water at 40℃; for 6h; | 25% |
Conditions | Yield |
---|---|
With potassium phosphate In tetrahydrofuran at 115℃; for 18h; | 100% |
With CF3-DPPF; bis(dibenzylideneacetone)-palladium(0) In tetrahydrofuran; toluene at 120℃; for 20h; | 79.6% |
With CF3-DPPF ligand; bis(dibenzylideneacetone)-palladium(0) In tetrahydrofuran; toluene at 120℃; for 30h; Product distribution; various DPPF ligands for the Pd-catalyzed formation of diaryl ethers; |
sodium phenoxide
6,7-dimethoxy-4-chloroquinazoline
6,7-dimethoxy-4-phenoxyquinazoline
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 80℃; for 3h; | 100% |
Conditions | Yield |
---|---|
Stage #1: 4-phenyl-butan-1-ol With 1,2-Diiodoethane; N,N-dimethyl-formamide; triphenylphosphine at 20℃; for 0.0166667h; Sealed tube; Inert atmosphere; Stage #2: sodium phenoxide at 20℃; Sealed tube; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 1h; | 99% |
perfluoro(propyl vinyl ether)
sodium phenoxide
(2-Chloro-1,1,2-trifluoro-2-heptafluoropropyloxy-ethoxy)-benzene
Conditions | Yield |
---|---|
With hexachloroethane In N,N-dimethyl-formamide 1) 25 deg C - 29 deg C, 2) r.t., overnight; | 99% |
4-nitro-N-methyl-phthalimide
sodium phenoxide
4-phenoxy-N-methyl phthalimide
Conditions | Yield |
---|---|
N-neopentyl chloride of 4-dibutylaminopyridine In toluene at 110℃; for 1h; | 99% |
In dimethyl sulfoxide at 15 - 120℃; for 24h; Inert atmosphere; | 93% |
sodium phenoxide
Conditions | Yield |
---|---|
In water a mixt. of Fe compd. and C6H5ONa in water is refluxed for 5 min; mixt. is cooled and extd. with ether, extract is washed with ether and dried with sodium sulfate, removal of ether by distillation, recrystn. from heptane; | 99% |
sodium phenoxide
diphenylcarbamic chloride
diphenyl-carbamic acid phenyl ester
Conditions | Yield |
---|---|
at 20℃; for 0.08h; Neat (no solvent); Microwave irradiation; Grinding; | 99% |
tert-butyl (3-bromo-5-chloropyrazolo[1,5-a]pyrimidin-7-yl)(2-morpholinoethyl)carbamate
sodium phenoxide
tert-butyl (3-bromo-5-phenoxypyrazolo[1,5-a]pyrimidin-7-yl)(2-morpholinoethyl)carbamate
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 0.5h; | 99% |
2-Amino-6-chlor-3,4,5-pyridintricarbonitril
sodium phenoxide
Conditions | Yield |
---|---|
In acetone for 0.5h; Heating; | 98% |
sodium phenoxide
Conditions | Yield |
---|---|
In tetrahydrofuran; water for 48h; Ambient temperature; | 98% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 98% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 100℃; | 98% |
sodium phenoxide
tetrachlorophenoxyphosphorane
Conditions | Yield |
---|---|
With phosphorus pentachloride In tetrachloromethane at -15℃; for 1h; | 98% |
biphenyl-4-yl methanol
sodium phenoxide
1-phenyl-4-phenoxymethylbenzene
Conditions | Yield |
---|---|
Stage #1: biphenyl-4-yl methanol With 1,2-Diiodoethane; N,N-dimethyl-formamide; triphenylphosphine at 20℃; for 0.0166667h; Sealed tube; Inert atmosphere; Stage #2: sodium phenoxide at 20℃; Sealed tube; Inert atmosphere; | 98% |
potassium phenolate
sodium phenoxide
2,2,4,4,6,6-hexaphenoxycyclotriphosphazene
Conditions | Yield |
---|---|
With cesium hydroxide; 2,2,4,4,6,6-hexachloro-1,3,5-triaza-2,4,6-triphosphorine In 1,2-dichloro-benzene at 175℃; Product distribution / selectivity; | 97.9% |
Conditions | Yield |
---|---|
at 105℃; pH=9 - 10; | 97.6% |
Conditions | Yield |
---|---|
at 120℃; for 6h; Temperature; | 97.5% |
Conditions | Yield |
---|---|
In tetrahydrofuran; diethyl ether for 1h; Ambient temperature; | 97% |
Conditions | Yield |
---|---|
N-2-ethylhexyl chloride of 4(4-methylpiperidinyl)pyridine In toluene at 110℃; for 0.25h; | 97% |
With ammonia at 25℃; Kinetics; Concentration; |
sodium phenoxide
A
1-methoxy-4-phenoxy-benzene
B
4-methoxy-7-iodo[2.2]paracyclophane
Conditions | Yield |
---|---|
In [D3]acetonitrile at 80℃; for 1h; Inert atmosphere; Darkness; regioselective reaction; | A 75% B 97% |
(S)-(1-benzyl-2,5-dihydro-1H-pyrrol-2-yl)methanol
sodium phenoxide
(R)-1-benzyl-3-phenoxy-1,2,3,6-tetrahydropyridine
Conditions | Yield |
---|---|
Stage #1: (S)-(1-benzyl-2,5-dihydro-1H-pyrrol-2-yl)methanol With trifluoromethylsulfonic anhydride In dichloromethane at -15℃; Inert atmosphere; Stage #2: sodium phenoxide In tetrahydrofuran; dichloromethane at -15 - 20℃; Inert atmosphere; optical yield given as %ee; regioselective reaction; | 97% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 36h; Inert atmosphere; Glovebox; | 97% |
sodium phenoxide
Conditions | Yield |
---|---|
In water; acetone at 20℃; for 12h; Schlenk technique; | 97% |
4,5-dichloro-1-phenylpyridazin-6-one
sodium phenoxide
5-chloro-4-phenoxy-2-phenyl-2H-pyridazin-3-one
Conditions | Yield |
---|---|
In 1,4-dioxane for 16h; Ambient temperature; | 96% |
(2-13C)bromoacetic acid
sodium phenoxide
<2-13C>-2-phenoxyacetic acid
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran for 2h; Heating; | 96% |
bis(4-methylbenzenethiocarbonyl) sulphide
sodium phenoxide
O-phenyl 4-methylbenzenecarbothioate
Conditions | Yield |
---|---|
In tetrahydrofuran; diethyl ether; ethanol for 3h; Ambient temperature; | 96% |
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