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:103-25-3
Min.Order:1 Kilogram
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Min.Order:1 Metric Ton
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Type:Manufacturers
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Min.Order:1 Kilogram
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Type:Trading Company
inquiryProduct Name Methyl 3-phenylpropionate Synonyms Methyl 3-phenylpropionate;3-Phenylpropionic acid methyl ester CAS: 103-25-3 MF: - MW: -
Cas:103-25-3
Min.Order:5 Metric Ton
FOB Price: $1.0 / 2.0
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Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryProduct Name: 3-Phenylpropionic acid methyl ester CAS: 103-25-3 MF: C10H12O2 MW: 164.2 EINECS: 203-092-2 Mol File: 103-25-3.mol 3-Phenylpropionic acid methyl ester Structure 3-Phenylpropionic acid methyl ester Chemical Properties
Cas:103-25-3
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryOur 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 prese
Cas:103-25-3
Min.Order:1 Kilogram
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inquiry3-Phenylpropionic acid methyl ester CAS:103-25-3 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 qualit
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Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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
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Min.Order:1 Kilogram
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inquiryPRODUCT DETAILS 3-Phenylpropionic acid methyl ester Basic information
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Type:Lab/Research institutions
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Min.Order:1 Kilogram
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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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Min.Order:1 Milligram
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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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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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inquiryLocated in Hangzhou National Hi-Tech Industrial Development Zone, zhongqichem is a technical company mainly focus on the Custom synthesis, manufacturing, sales of chemicals to various industries. Benefiting from the outstanding customer service and h
Conditions | Yield |
---|---|
With hydrogen; palladium In ethyl acetate at 25℃; under 760.051 Torr; for 1h; | 100% |
With hydrogen; polymer incarcerated platinum In tetrahydrofuran at 20℃; for 1h; atmospheric pressure; | 100% |
With hydrogen; palladium in polystyrene In tetrahydrofuran at 25℃; under 760.051 Torr; for 1h; | 100% |
Conditions | Yield |
---|---|
With methanol; samarium diiodide In tetrahydrofuran Inert atmosphere; | 100% |
With C28H28Cl2N4Pd; hydrogen In methanol at 30 - 35℃; under 760.051 Torr; for 8h; chemoselective reaction; | 100% |
With hydrogen In methanol; ethanol at 25℃; under 2068.65 Torr; for 8h; Inert atmosphere; | 99.9% |
Conditions | Yield |
---|---|
With 4-methyl-morpholine; N-[4-methoxy-6-(N'-phenylbenzamido)-1,3,5-triazin-2-yl]-N-methylmorpholinium chloride at 20℃; for 3h; Reagent/catalyst; | 100% |
With 4-(1H,1H-perfluorotetradecyl)-C6F4-CH(SO2CF3)2 at 70℃; for 7h; | 99% |
With sulfuric acid for 5h; Reflux; | 99% |
methanol
ethyl dihydrocinnamate
A
ethanol
B
3-phenylpropanoic acid methyl ester
Conditions | Yield |
---|---|
2[{Cl(C6F13CH2CH2)2SnOSn(CH2CH2C6F13)2Cl}2] In various solvent(s) at 150℃; for 16h; | A n/a B 100% |
methanol
Benzyl 3-phenylpropionate
A
3-phenylpropanoic acid methyl ester
B
benzyl alcohol
Conditions | Yield |
---|---|
2[{Cl(C6F13CH2CH2)2SnOSn(CH2CH2C6F13)2Cl}2] In various solvent(s) at 150℃; for 16h; | A 100% B n/a |
Conditions | Yield |
---|---|
[Cl(C6F13C2H4)2SnOSn(C2H4C6F13)2Cl]2 In various solvent(s) at 150℃; for 16h; | 100% |
at 400℃; under 135014 Torr; for 0.05h; Temperature; Supercritical conditions; Flow reactor; | 92% |
With dipotassium hydrogenphosphate for 5h; Reflux; | 88% |
at 350℃; under 135014 Torr; Continuous-flow; | 85% |
Conditions | Yield |
---|---|
[Cl(C6F13C2H4)2SnOSn(C2H4C6F13)2Cl]2 In various solvent(s) at 150℃; for 16h; | 100% |
With dipotassium hydrogenphosphate for 24h; Reflux; | 98% |
methyl 3-phenyl-2-(dimethylsilyl)propanoate
3-phenylpropanoic acid methyl ester
Conditions | Yield |
---|---|
With tetrabutylammonium tetrafluoroborate In acetonitrile Electrolysis; | 100% |
methanol
(S)-(2,3,4,5,6-pentafluorophenyl) 3-phenylpropanethioate
3-phenylpropanoic acid methyl ester
Conditions | Yield |
---|---|
With potassium carbonate at 50℃; for 0.5h; | 100% |
carbonic acid dimethyl ester
3-Phenylpropionic acid
3-phenylpropanoic acid methyl ester
Conditions | Yield |
---|---|
With Novozym 435; acylase I from Aspergillus melleus; amano lipase AK from pseudomonas fluorescens; lipase from wheat germ; papaine In toluene at 40℃; for 48h; Mechanism; Enzymatic reaction; | 100% |
With sulfuric acid at 80 - 85℃; for 5h; Neat (no solvent); | 99.8% |
Conditions | Yield |
---|---|
With C28H28Cl2N4Pd; hydrogen at 30 - 35℃; under 760.051 Torr; for 8h; chemoselective reaction; | 100% |
Conditions | Yield |
---|---|
With manganese(IV) oxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1,4-dimethyl-1,2,4-triazolium iodide at 20℃; Inert atmosphere; | 99% |
With manganese(IV) oxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1,4-dimethyl-1,2,4-triazolium iodide In dichloromethane at 20℃; Inert atmosphere; | 98% |
With urea hydrogen peroxide adduct; p-toluenesulfonyl chloride at 60℃; for 8h; | 98% |
Conditions | Yield |
---|---|
With methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; samarium diiodide In tetrahydrofuran at 0 - 20℃; for 0.25h; Deamination; | 99% |
methanol
phenethylamine
3-Phenylpropionic acid
A
3-phenylpropanoic acid methyl ester
B
N-phenethyl-3-phenylpropanamide
Conditions | Yield |
---|---|
With 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride at 20℃; for 3h; | A 1% B 98% |
With 2-chloro-4-(1,3-dioxoisoindolin-2-yl)-6-methoxy-1,3,5-triazine at 20℃; for 3h; Reagent/catalyst; | A 15 %Spectr. B 67 %Spectr. |
With 4-methyl-morpholine; 4-[4,6-bis(2,6-dimethylphenyl)-1,3,5-triazin-2-yl]-4-methylmorpholinium perchlorate at 20℃; for 3h; Reagent/catalyst; | A 6 %Spectr. B 91 %Spectr. |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 10h; Inert atmosphere; | 98% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile for 8h; Heating; | 84% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile for 8h; Reflux; | 84% |
Conditions | Yield |
---|---|
With 2-mesityl-2,5,6,7-tetrahydropyrrolo[2,1-c][1,2,4]triazol-4-ium; N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 60℃; for 24h; | 97% |
With triethylamine; 2-hydroxy-2-methylpropanenitrile at 25℃; for 3h; | 93% |
Stage #1: (E)-3-phenylpropenal With trimethylsilyl cyanide; 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 28℃; for 3.5h; Stage #2: methanol In acetonitrile | 67% |
Stage #1: (E)-3-phenylpropenal With trimethylsilyl cyanide; tris(2,4,6-trimethoxyphenyl)phosphine In acetonitrile at 28℃; for 6h; Stage #2: methanol In acetonitrile at 20℃; for 3h; | 63% |
sodium methylate
(4S)-3-(3-phenylpropionyl)-4-(2-propyl)oxazolidin-2-one
A
3-phenylpropanoic acid methyl ester
B
(4S)-4-isopropyl-1,3-oxazolidin-2-one
Conditions | Yield |
---|---|
With carbonic acid dimethyl ester In dichloromethane at 20℃; for 0.75h; | A 97% B n/a |
sodium methylate
(S)-N-(1-hydroxy-3-methylbutan-2-yl)-3-phenylpropanamide
A
3-phenylpropanoic acid methyl ester
B
(4S)-4-isopropyl-1,3-oxazolidin-2-one
Conditions | Yield |
---|---|
With carbonic acid dimethyl ester In dichloromethane at 20℃; for 1h; | A 97% B n/a |
diazomethane
3-Phenyl-1-propanol
3-phenylpropanoic acid methyl ester
Conditions | Yield |
---|---|
Stage #1: 3-Phenyl-1-propanol With sodium chlorite; sodium dihydrogenphosphate; Me-AZADO+Cl- In dichloromethane; water at 25℃; for 1.5h; Stage #2: With 2-methyl-but-2-ene In dichloromethane; water Stage #3: diazomethane With hydrogenchloride; sodium hydroxide Product distribution / selectivity; more than 3 stages; | 97% |
Stage #1: 3-Phenyl-1-propanol With sodium chlorite; sodium dihydrogenphosphate; 2,2,6,6-tetramethylpiperidin-1-oxoammonium chloride In dichloromethane; water at 25℃; for 1.5h; Stage #2: With 2-methyl-but-2-ene In dichloromethane; water Stage #3: diazomethane With hydrogenchloride; sodium hydroxide Product distribution / selectivity; more than 3 stages; | 77% |
methanol
1,1,1,3,3,3-hexafluoropropan-2-yl 3-phenylpropanoate
3-phenylpropanoic acid methyl ester
Conditions | Yield |
---|---|
With triethylamine at 20℃; for 12h; | 97% |
phenethylamine
benzoic acid
A
3-phenylpropanoic acid methyl ester
B
N-phenethylbenzamide
Conditions | Yield |
---|---|
With N-[4-methoxy-6-(N'-phenylbenzamido)-1,3,5-triazin-2-yl]-N-methylmorpholinium chloride In methanol at 20℃; for 4h; | A 8 %Spectr. B 97% |
3-phenyl-N-(quinoline-8-yl)propionamide
methanol
3-phenylpropanoic acid methyl ester
Conditions | Yield |
---|---|
With nickel(II) bis(2,2,6,6-tetramethylheptane-3,5-dionate) at 100℃; for 24h; Reagent/catalyst; chemoselective reaction; | 97% |
With nickel(II) bis(2,2,6,6-tetramethylheptane-3,5-dionate) at 80℃; for 72h; Catalytic behavior; Time; Inert atmosphere; Schlenk technique; |
2-benzyl-malonic acid dimethyl ester
3-phenylpropanoic acid methyl ester
Conditions | Yield |
---|---|
With lithium chloride In various solvent(s) at 160℃; for 12h; | 95% |
With hydrogenchloride; water |
N,N’-diisopropyl-O-methylisourea
3-Phenylpropionic acid
A
1,3-diisopropylurea
B
3-phenylpropanoic acid methyl ester
Conditions | Yield |
---|---|
In acetonitrile at 120℃; for 0.0333333h; Microwave irradiation; | A n/a B 95% |
methanol
1-(1-methyl-1H-imidazol-2-yl)-3-phenylpropan-1-one
3-phenylpropanoic acid methyl ester
Conditions | Yield |
---|---|
at 150℃; for 15h; Reagent/catalyst; Autoclave; Inert atmosphere; | 95% |
1-t-butyldioxy-1-methoxy-3-phenylpropane
3-phenylpropanoic acid methyl ester
Conditions | Yield |
---|---|
In methanol at 60℃; | 94% |
methanol
vinyl ester of 3-phenylpropionic acid
3-phenylpropanoic acid methyl ester
Conditions | Yield |
---|---|
With KCl-Subtilisin Bacillus lentus In acetonitrile for 24h; Ambient temperature; | 94% |
sodium methylate
(S)-ethyl 4,4-dimethyl-N-(3-phenylpropionyl)pyroglutamate
3-phenylpropanoic acid methyl ester
Conditions | Yield |
---|---|
In methanol at 20℃; for 1h; | 94% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; silica gel; cyclohexene In ethyl acetate at 120℃; for 0.333333h; Flow reactor; | 94% |
With magnesium; zinc(II) chloride for 0.5h; | 88% |
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid at 25℃; for 48h; | 100% |
With phosphoric acid; phosphorus pentoxide | |
With trifluorormethanesulfonic acid at 32℃; Kinetics; | |
With trifluorormethanesulfonic acid at 25℃; Cooling with ice; |
3-phenylpropanoic acid methyl ester
tert-butyl alcohol
tert-butyl 3-phenylpropanoate
Conditions | Yield |
---|---|
Zn4O (OCOCF3)6(CF3COOH)n In di-isopropyl ether for 18h; Product distribution / selectivity; Inert atmosphere; Reflux; | 100% |
With (μ-oxo)bis[(1,2-ethanediamino-N,N'-bis(salicylidene))iron(III)] In 5,5-dimethyl-1,3-cyclohexadiene at 150℃; for 24h; Catalytic behavior; Reagent/catalyst; Temperature; Inert atmosphere; Schlenk technique; chemoselective reaction; | 97% |
With FeIII-salen In 5,5-dimethyl-1,3-cyclohexadiene at 150℃; for 24h; Temperature; Reagent/catalyst; | 86% |
With indium; iodine for 22h; transesterification; Heating; sonication; | 68% |
3-phenylpropanoic acid methyl ester
Se-methyl selenohydrocinnamate
Conditions | Yield |
---|---|
In dichloromethane; toluene 1.) 0 deg C, 30 min, 2.) 30 min; | 100% |
ethanol
3-phenylpropanoic acid methyl ester
A
methanol
B
ethyl dihydrocinnamate
Conditions | Yield |
---|---|
2[{Cl(C6F13CH2CH2)2SnOSn(CH2CH2C6F13)2Cl}2] In various solvent(s) at 150℃; for 16h; | A n/a B 100% |
3-Phenylpropenol
3-phenylpropanoic acid methyl ester
A
methanol
B
3-phenyl-2-propenyl benzenepropanoate
Conditions | Yield |
---|---|
2[{Cl(C6F13CH2CH2)2SnOSn(CH2CH2C6F13)2Cl}2] In various solvent(s) at 150℃; for 16h; | A n/a B 100% |
3-phenylpropanoic acid methyl ester
8-(tert-butyldimethylsiloxy)octan-1-ol
A
methanol
Conditions | Yield |
---|---|
2[{Cl(C6F13CH2CH2)2SnOSn(CH2CH2C6F13)2Cl}2] In various solvent(s) at 150℃; for 16h; | A n/a B 100% |
Conditions | Yield |
---|---|
[Cl(C6F13C2H4)2SnOSn(C2H4C6F13)2Cl]2 In various solvent(s) at 150℃; for 16h; | 100% |
With potassium phosphate; N-benzyl-N,N,N-triethylammonium chloride at 20℃; for 3h; | 96% |
With potassium carbonate; dibromotriphenylphosphorane In acetonitrile for 24h; Reflux; | 70% |
With dipotassium hydrogenphosphate for 24h; Reflux; |
3-Phenylpropenol
3-phenylpropanoic acid methyl ester
3-phenyl-2-propenyl benzenepropanoate
Conditions | Yield |
---|---|
[Cl(C6F13C2H4)2SnOSn(C2H4C6F13)2Cl]2 In various solvent(s) at 150℃; for 16h; | 100% |
With zinc diacetate In toluene for 18h; Reflux; |
3-phenylpropanoic acid methyl ester
benzyl alcohol
Benzyl 3-phenylpropionate
Conditions | Yield |
---|---|
[Cl(C6F13C2H4)2SnOSn(C2H4C6F13)2Cl]2 In toluene for 6h; Heating; | 100% |
With Zn4(OCOCF3)6O In toluene for 18h; Heating; | 95% |
With potassium phosphate; N-benzyl-N,N,N-triethylammonium chloride for 24h; Reflux; | 79% |
3-phenylpropanoic acid methyl ester
(S)-tert-leucinol
(S)-2-phenethyl-4-tert-butyloxazoline
Conditions | Yield |
---|---|
Zn4(OCOCF3)6O In chlorobenzene for 18h; Product distribution / selectivity; Heating / reflux; | 100% |
With Zn4(OCOCF3)6O In chlorobenzene for 18h; Heating; | 99% |
3-phenylpropanoic acid methyl ester
butan-1-ol
3-phenyl-propionic acid butyl ester
Conditions | Yield |
---|---|
Zn4O (OCOCF3)6(CF3COOH)n In di-isopropyl ether for 18h; Product distribution / selectivity; Inert atmosphere; Reflux; | 100% |
With Zn4(OCOCF3)6O In di-isopropyl ether for 18h; Heating; | 92% |
With zinc diacetate In toluene for 18h; Reflux; | 74% |
With potassium carbonate; dibromotriphenylphosphorane In acetonitrile for 24h; Reflux; | 60% |
3-phenylpropanoic acid methyl ester
cyclohexanol
cyclohexyl 3-phenylpropionate
Conditions | Yield |
---|---|
With cyclohexylamine; Zn4O (OCOCF3)6(CF3COOH)n In di-isopropyl ether for 18h; Inert atmosphere; Reflux; | 100% |
With Co2(μ2-OCH2C6H4-4-CH3)2(η2-OCOtBu)2(2,2’-bipyridine)2; para-methylbenzylamine In toluene for 18h; Reflux; Inert atmosphere; Schlenk technique; chemoselective reaction; | 40% |
With Zn(2+)*2C3F5O2(1-)*2H2O In di-isopropyl ether for 25h; Reagent/catalyst; Reflux; Inert atmosphere; Schlenk technique; | 60 %Chromat. |
Conditions | Yield |
---|---|
With samarium diiodide; 18O-labeled water; triethylamine In tetrahydrofuran at 20℃; for 2h; Reagent/catalyst; Inert atmosphere; Schlenk technique; | 99% |
With C32H36ClNO2P2Ru; potassium tert-butylate; hydrogen In tetrahydrofuran at 120℃; under 38002.6 Torr; for 20h; Autoclave; Green chemistry; | 99% |
Stage #1: 3-phenylpropanoic acid methyl ester With dimethylethylsilane; (μ3,η2:η3:η5-acenaphthalene)Ru3(CO)7 In 1,4-dioxane at 20℃; for 0.5h; Stage #2: With hydrogenchloride In 1,4-dioxane; water Further stages.; | 97% |
Conditions | Yield |
---|---|
With iodine; aluminium In acetonitrile at 80℃; for 18h; | 99% |
With NaSiO(CH3)3 In tetrahydrofuran at 20℃; for 2h; | 95% |
With water; triethylamine; lithium bromide In acetonitrile at 20℃; for 48h; | 89% |
3-phenylpropanoic acid methyl ester
benzylamine
N-benzyl-3-phenylpropanamide
Conditions | Yield |
---|---|
With Sphingomonas sp. HXN-200 lipase In hexane; water at 30℃; for 20h; Reagent/catalyst; Enzymatic reaction; | 99% |
With 1-hydroxy-7-aza-benzotriazole; zirconium(IV) tert-butoxide In toluene at 20℃; Kinetics; | |
With 1-hydroxy-7-aza-benzotriazole; zirconium(IV) tert-butoxide In toluene at 20℃; | |
With μ4-oxo-hexakis(μ-acetato)tetrazinc In 5,5-dimethyl-1,3-cyclohexadiene for 20h; Reagent/catalyst; Reflux; Inert atmosphere; Schlenk technique; | 36 %Chromat. |
1-octadecanol
3-phenylpropanoic acid methyl ester
octadecyl 3-phenylpropionate
Conditions | Yield |
---|---|
With Zn4(OCOCF3)6O In di-isopropyl ether for 18h; Heating; | 99% |
With potassium phosphate; N-benzyl-N,N,N-triethylammonium chloride In toluene for 48h; Reflux; | 69% |
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