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:4748-78-1
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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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Cas:4748-78-1
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inquiryProduct Name: 4-Ethylbenzaldehyde Synonyms: ethylbenzaldehyde,4-ethylbenzaldehyde;4-ETHYLBENZALDEHYDE 98+%;4-Ethylbenzaldehyde,90%;4-Ethylbenzaldehyde,99%;4-Ethylbenzaldehyde, 98% 25GR;4-ethyl-benzaldehyd;Benzaldehyde,4-ethyl;Ebal CAS: 4748-78-1
Cas:4748-78-1
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inquiryOur 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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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
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inquiryHangzhou 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
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inquiryJ&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
supplier in China Appearance:clear colourless to slightly yellow liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:100g/bottle,1kg/bottle,25kg/drum or as per your request Application:Used as Pharmaceutica
4-Ethylbenzaldehyde Chemical Properties Boiling point 221 °C (lit.) density 0.979 g/mL at 25 °C (lit.) FEMA 3756 | 4-ETHYLBENZALDEHYDE refractive index n20/D 1.539(lit.) Fp 198 °F form Liquid color Clear colorl
Cas:4748-78-1
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inquiryfactory?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
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inquiry1.We only supply pure OLED intermediates,quality guranteen; 2.Worldwide fast delivery;3.Much stock;106.Feasible payment methodAppearance:solid or liquid Storage:in RT Package:drum and foil bag Application:This substance is used widely in oled interme
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Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
Cas:4748-78-1
Min.Order:100 Gram
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inquiryAcmec is a leading manufacturer and supplier of biochemical reagents and life science products. We have over 40,000 items in stock (real-time inventory) and offer discounted prices to registered members of the online store ( www.acmec.com.cn ) Appea
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inquiryhigh quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
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Cas:4748-78-1
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inquiryHunan chemfish Pharmaceutical co.,Ltd.located in Lugu High-tech industral park ,Hunan province . with its own R&D center and more than 10000㎡manufacture plant . Chemfish owns 40 reactors from 1000L to 8000L. With complete auxiliary equipment as
Conditions | Yield |
---|---|
With hydrogen In tetrahydrofuran at 50℃; under 760.051 Torr; for 10h; | A 97% B 3% |
With hydrogen In dichloromethane at 40℃; under 1500.15 Torr; for 24h; Reagent/catalyst; Solvent; Temperature; Pressure; Schlenk technique; | A 67 %Chromat. B 33 %Chromat. |
Conditions | Yield |
---|---|
With iron(III) chloride; nitric acid In acetone at 20℃; for 0.233333h; Sonication; | 95% |
With 3,3-dichloro-1,2-diphenylcyclopropene; dimethyl sulfoxide; triethylamine In dichloromethane at -78 - 20℃; Inert atmosphere; | 95% |
With laccase; 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt In tetrahydrofuran; water at 40℃; for 24h; | 92% |
Conditions | Yield |
---|---|
With immobilised amine transaminase from the moderate halophilic bacterium Halomonas elongata; sodium pyruvate In aq. phosphate buffer; dimethyl sulfoxide at 37℃; under 760.051 Torr; for 2h; pH=8; | 94% |
With steam; nickel at 210℃; |
1-bromo-4-ethylbenzene
N,N-dimethyl-formamide
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With samarium; copper(l) iodide at 20℃; for 4h; Inert atmosphere; | 93% |
Conditions | Yield |
---|---|
With dihydrogen peroxide In acetonitrile at 65℃; for 6h; | 92% |
Conditions | Yield |
---|---|
With methanol; formic acid; water In ethyl acetate at 25℃; for 3h; Irradiation; Inert atmosphere; | 90% |
With aluminum (III) chloride In ethanol; water; acetonitrile at 20℃; for 6h; Irradiation; Inert atmosphere; | 95 %Chromat. |
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With sodium tetrahydroborate; nickel(II) chloride hexahydrate In methanol at 20℃; for 2.5h; chemoselective reaction; | 86% |
Conditions | Yield |
---|---|
With succinic acid anhydride; methylphenylsilane; C58H82O6P2; copper(II) nitrate In tetrahydrofuran at 75℃; for 18h; Schlenk technique; Inert atmosphere; | 85% |
With potassium phosphate; sodium hypophosphite; 2,2-dimethylpropanoic anhydride; palladium diacetate; tricyclohexylphosphine In tetrahydrofuran at 60℃; for 16h; | 74% |
With 2,6-dimethylpyridine; nickel(II) bromide trihydrate; phenylsilane; 4,4'-di-tert-butyl-2,2'-bipyridine; zinc; dimethyl dicarbonate In ethyl acetate at 60℃; for 24h; Schlenk technique; Inert atmosphere; | 76 %Chromat. |
Conditions | Yield |
---|---|
Stage #1: formic acid; 4-ethyl-1-iodobenzene With palladium diacetate; acetic anhydride; tricyclohexylphosphine In N,N-dimethyl-formamide at 30℃; for 1h; Inert atmosphere; Green chemistry; Stage #2: With triethylamine In N,N-dimethyl-formamide at 80℃; for 6h; Inert atmosphere; Green chemistry; | 85% |
With palladium diacetate; triethylamine; dicyclohexyl-carbodiimide; tricyclohexylphosphine In N,N-dimethyl-formamide at 80℃; for 10h; Inert atmosphere; Sealed tube; | 71% |
Conditions | Yield |
---|---|
at 100℃; for 5h; | 80% |
Conditions | Yield |
---|---|
Stage #1: carbon dioxide With zinc(II) cyanide; ruthenium trichloride; rhodium (III) acetate; cobalt(II) acetate; zirconium(IV) acetate for 1h; Autoclave; Stage #2: ethylbenzene at 50℃; under 15001.5 Torr; for 5h; | 80% |
triethyl borane
4-(trifluormethanesulfonyloxy)benzaldehyde
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; cesium acetate In tetrahydrofuran Suzuki-Miyaura cross-coupling; Reflux; Inert atmosphere; | 78% |
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With 4-ethylbenzyl alcohol; 1,2-dimethylindazolium chloride for 3h; Heating; | 71% |
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide at 120℃; for 5h; Sealed tube; Green chemistry; | 70% |
p,p'-diethyldiphenylmercury
N,N-dimethyl-formamide
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With trichlorophosphate In water at 70℃; for 5h; | 65% |
ethyllithium
4-bromo-N-methoxy-N-methylbenzamide
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
Stage #1: 4-bromo-N-methoxy-N-methylbenzamide With diisobutylaluminium hydride In hexane; toluene at 0 - 20℃; Inert atmosphere; Schlenk technique; Stage #2: ethyllithium In hexane; toluene at 20℃; Inert atmosphere; Schlenk technique; | 61% |
Conditions | Yield |
---|---|
With (1,2-dimethoxyethane)dichloronickel(II); N,N,N,N,-tetramethylethylenediamine; (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate; water; N-ethyl-N,N-diisopropylamine In dimethyl sulfoxide at 80℃; under 760.051 Torr; for 24h; Schlenk technique; Sealed tube; Irradiation; | 54% |
Conditions | Yield |
---|---|
With (1,2-dimethoxyethane)dichloronickel(II); N,N,N,N,-tetramethylethylenediamine; (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate; water; N-ethyl-N,N-diisopropylamine In dimethyl sulfoxide at 80℃; under 760.051 Torr; for 24h; Schlenk technique; Sealed tube; Irradiation; | 50% |
4-ethyl-1-cyclopropylbenzene
A
(E)-3-(4-ethylphenyl)acrylaldehyde
B
5-(4-ethylphenyl)isoxazoline
C
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With dinitrogen tetraoxide; triethylamine In dichloromethane at -30℃; for 1h; | A 32% B 48% C 8% |
With dinitrogen tetraoxide In dichloromethane at -30℃; for 1h; | A 35% B 40% C 8% |
1-cyclopropyl-4-methyl-benzene
A
(E)-3-(4-ethylphenyl)acrylaldehyde
B
5-(4-ethylphenyl)isoxazoline
C
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With dinitrogen tetraoxide In dichloromethane at -30℃; for 1h; | A 35% B 40% C 8% |
(4-ethyl-benzyliden)-aniline
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With sulfuric acid | |
With sulfuric acid |
N-(4-ethyl-benzylidene)-p-toluidine
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With sulfuric acid |
Conditions | Yield |
---|---|
With hexamethylenetetramine |
Conditions | Yield |
---|---|
With oxygen; iron(II) chloride; zinc; iron(III) In pyridine; acetic acid for 16h; | A 10.3 % Chromat. B 3.1 % Chromat. |
With oxygen; acetic acid; iron(II) chloride; zinc; iron(III) In pyridine for 16h; Product distribution; other alkylbenzenes; without Fe(III)-catalyst; | |
With oxygen In acetonitrile at 24.84℃; under 760.051 Torr; Reagent/catalyst; Irradiation; Green chemistry; |
4-methylethylbenzene
A
1-ethenyl-4-methylbenzene
B
CH3C6H4CH(CH3)OH
C
para-methylacetophenone
D
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With ammonium peroxydisulfate; copper diacetate In water; acetonitrile at 100℃; Yield given. Further byproducts given. Yields of byproduct given; | |
With ammonium peroxydisulfate; copper diacetate; sodium acetate In water; acetonitrile at 100℃; Yield given. Further byproducts given. Yields of byproduct given; |
4-methylethylbenzene
A
1-ethenyl-4-methylbenzene
B
4-ethylbenzyl acetate
C
para-methylacetophenone
D
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With ammonium peroxydisulfate; copper diacetate In water; acetic acid at 100℃; Yield given. Further byproducts given. Yields of byproduct given; |
N-tert-butyl α-(4-ethylphenyl) nitrone
A
N-tert-Butylhydroxylamine
B
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With water at 25℃; Rate constant; hydrolysis; |
Conditions | Yield |
---|---|
With water; hydrogen cation In various solvent(s) at 25℃; Rate constant; Mechanism; pH=1.00; rate constant - octanol/water partition coefficient and relative rate - substituent constants correlations in lamellar solvent; |
4-methylethylbenzene
A
1-ethenyl-4-methylbenzene
B
4-ethylbenzyl alcohol
C
para-methylacetophenone
D
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With nitrate radical under 760 Torr; Kinetics; Oxidation; |
4-Butylaniline
4-ethylbenzylaldehyde
4-butyl-N-[(1E)-(4-ethylphenyl)methylene]aniline
Conditions | Yield |
---|---|
In ethanol Reflux; Inert atmosphere; | 100% |
propylamine
4-ethylbenzylaldehyde
N-(4-ethylbenzylidene)propan-1-amine
Conditions | Yield |
---|---|
at 20℃; for 12h; | 100% |
at 20℃; for 1h; |
Conditions | Yield |
---|---|
at 20℃; for 12h; | 100% |
at 20℃; for 1h; | |
In dichloromethane at 20℃; for 4h; |
ketene t-butyldimethylsilyl methyl acetal
4-ethylbenzylaldehyde
C18H30O3Si
Conditions | Yield |
---|---|
With silver hexafluoroantimonate; 2,6-bis-[1-(2,6-diethylphenylimino)ethyl]pyridine iron(II) chloride In dichloromethane at 20℃; Mukaiyama Aldol Addition; Inert atmosphere; | 100% |
With C33H29FeNO2P(1+)*I(1-) In acetonitrile at 20℃; for 0.25h; Mukaiyama aldol reaction; | 48% |
cis, trans-1,3-dimethylaminocyclohexane
4-ethylbenzylaldehyde
C26H34N2
Conditions | Yield |
---|---|
In methanol at 20℃; Molecular sieve; | 100% |
In methanol at 20℃; Molecular sieve; |
Conditions | Yield |
---|---|
at 20℃; | 100% |
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol at 20℃; for 15h; Claisen-Schmidt Condensation; | 100% |
Conditions | Yield |
---|---|
With sodium tetrahydroborate In methanol at 0℃; for 0.25h; | 99% |
With formaldehyd; C42H36ClIrO2P2; triethylamine In 1,2-dimethoxyethane at 80℃; for 20h; Reagent/catalyst; Schlenk technique; Inert atmosphere; chemoselective reaction; | 99% |
With sodium tetrahydroborate In methanol for 14h; | 98% |
Conditions | Yield |
---|---|
With ammonium acetate; acetic acid for 1h; Reflux; stereoselective reaction; | 99% |
With ammonium acetate; acetic acid for 1 - 12h; Heating / reflux; |
triethylsilane
4-ethylbenzylaldehyde
triethyl((4-ethylbenzyl)oxy)silane
Conditions | Yield |
---|---|
With C42H43BN3P2(1+)*C18HBF15(1-) In chloroform at 40℃; for 1h; Reagent/catalyst; Temperature; Schlenk technique; Glovebox; | 99% |
para-chloroacetophenone
4-ethylbenzylaldehyde
(2E)-1-(4-chlorophenyl)-3-(4-ethylphenyl)prop-2-en-1-one
Conditions | Yield |
---|---|
Stage #1: para-chloroacetophenone; 4-ethylbenzylaldehyde With sodium methylate In methanol at 20℃; for 16h; Stage #2: With hydrogenchloride In methanol; water | 98% |
With potassium hydroxide In ethanol at 20℃; Claisen-Schmidt Condensation; |
para-chloroacetophenone
4-ethylbenzylaldehyde
1-(4-chloro-phenyl)-3-(4-ethyl-phenyl)-propenone
Conditions | Yield |
---|---|
Stage #1: para-chloroacetophenone; 4-ethylbenzylaldehyde With sodium methylate In methanol at 20℃; for 16h; Stage #2: With hydrogenchloride In methanol; water | 98% |
1-deoxy-1-(methylamino)-D-glucitol
4-ethylbenzylaldehyde
(2R,5S)-2-(4-ethylphenyl)-3-methyl-5-(D-arabino-1,2,3,4-tetrahydroxybutyl)oxazolidine
Conditions | Yield |
---|---|
In benzene Heating; | 98% |
phenylhydrazine
4-ethylbenzylaldehyde
1-(4-ethylbenzylidene)-2-phenylhydrazine
Conditions | Yield |
---|---|
With pyridinium p-toluenesulfonate In dichloromethane | 98% |
In dichloromethane at 20℃; for 0.5h; | |
In ethanol; water at 80℃; |
Conditions | Yield |
---|---|
With cyclohexane-1,2-dione hydrolase In aq. buffer at 30℃; for 48h; pH=6.5; Enzymatic reaction; | 98% |
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol; water at 20℃; for 4h; | 98% |
Conditions | Yield |
---|---|
With sodium acetate In ethanol for 1h; Reflux; | 98% |
Conditions | Yield |
---|---|
With (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate In water at 20℃; for 3h; Schlenk technique; Inert atmosphere; Irradiation; Green chemistry; | 98% |
Conditions | Yield |
---|---|
With yttria doped hydroxyapatites In ethanol at 20℃; Reagent/catalyst; Temperature; Green chemistry; | 98% |
Conditions | Yield |
---|---|
With hydrazine hydrate In water at 60℃; for 0.75h; Green chemistry; | 98% |
Conditions | Yield |
---|---|
Stage #1: p-toluene sulfinic acid; 4-ethylbenzylaldehyde In water at 20℃; for 0.416667h; Stage #2: urea In water at 20℃; for 20h; | 98% |
4-ethylbenzylaldehyde
1,4-phenylenediamine
bis(4-ethylbenzylidene)-p-phenylenediamine
Conditions | Yield |
---|---|
In ethanol for 3h; | 97% |
In methanol |
4-Butylaniline
4-ethylbenzylaldehyde
N-(4-n-ethylbenzylidene)-4'-n-butylaniline
Conditions | Yield |
---|---|
97% |
4-ethylbenzylaldehyde
sodium (4-ethylphenyl)(hydroxy)methanesulfonate
Conditions | Yield |
---|---|
With sodium hydrogensulfite In ethanol; water for 20.5h; Inert atmosphere; | 97% |
With sodium metabisulfite; water In ethanol Cooling; |
benzoic acid hydrazide
allyl bromide
4-ethylbenzylaldehyde
N'-[1-(4-ethylphenyl)but-3-en-1-yl]benzohydrazide
Conditions | Yield |
---|---|
With zinc perchlorate; indium In methanol at 20℃; for 4h; chemoselective reaction; | 97% |
[(p-methylphenyl)sulfonylmethyl]isonitrile
4-ethylbenzylaldehyde
Conditions | Yield |
---|---|
With potassium carbonate at 80℃; for 1.5h; | 97% |
Conditions | Yield |
---|---|
With biguanide-functionalized hierarchical porous covalent organic framework In water at 20℃; for 0.166667h; Knoevenagel Condensation; | 97% |
With dimethyl 3-methyl-9-oxo-7-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)-2,4-di(pyridin-2-yl)-3,7-diazabicyclo-[3.3.1]nonane-1,5-dicarboxylate In water at 40℃; for 2h; Knoevenagel Condensation; | 95% |
Stage #1: 4-ethylbenzylaldehyde With C9H11ClN2O*ClHO4 In neat (no solvent) for 0.166667h; Knoevenagel Condensation; Stage #2: malononitrile In neat (no solvent) at 25 - 30℃; for 0.5h; Knoevenagel Condensation; | 94% |
Methyl diethylphosphonoacetate
4-ethylbenzylaldehyde
3-(4-ethylphenyl)acrylic acid methyl ester
Conditions | Yield |
---|---|
Stage #1: Methyl diethylphosphonoacetate With n-butyllithium In tetrahydrofuran; hexane at 0℃; for 0.5h; Inert atmosphere; Stage #2: 4-ethylbenzylaldehyde In tetrahydrofuran; hexane at 20℃; Inert atmosphere; | 97% |
Conditions | Yield |
---|---|
With 2.5 wt% vanadium oxide loaded on fluorapatite In ethanol at 20℃; for 0.5h; Green chemistry; | 97% |
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