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Cas:28785-06-0
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Min.Order:10 Gram
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
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4-Propylbenzaldehyde cas 28785-06-0Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
good quality, competitive price, thoughtful after sale serviceAppearance:white powder Storage:Keep it in dry,shady and cool place Package:1g Application:Pharma;Industry;Agricultural;chemical reaserch Transportation:by express or by sea Port:Any port
The factory supplies Application:manufacturing supplies
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
sodium tetrakis[(3,5-di-trifluoromethyl)phenyl]borate In water at 30℃; for 0.0833333h; | 100% |
4-n-propylbenzaldehyde diethyl acetal
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
In(OSO2CF3)3 In acetone at 20℃; for 0.5h; | 94% |
With acetic acid In water for 17h; Heating; | 91% |
With trifluoroacetic acid In dichloromethane at 25℃; for 20h; | 83% |
With hydrogenchloride In tetrahydrofuran for 6.5h; Heating; |
1-propyl-1,3,5,7-cyclooctatetraene
A
4-n-propylbenzaldehyde
B
2-propylbenzaldehyde
C
3-propylbenzaldehyde
Conditions | Yield |
---|---|
With oxygen; copper(l) chloride; palladium dichloride In tetrahydrofuran; water at 60℃; for 6h; | A 5% B 15% C 80% |
Conditions | Yield |
---|---|
With trifluoroacetic acid at 80℃; Heating; | 70% |
In trifluoroacetic acid at 80℃; |
1-(Chloromethyl)-4-propylbenzene
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
With hexamethylenetetramine In acetic acid | |
With ethanol; hexamethylenetetramine |
Conditions | Yield |
---|---|
With aluminium trichloride; hydrogen; palladium on activated charcoal 1.) tetrachloroethane, rt, 30 min; 2.) 100 deg C, normal pressure or 50 deg C, 30 atm; AcONa can be added; Multistep reaction; |
Conditions | Yield |
---|---|
With titanium tetrachloride In chloroform at -20℃; for 0.75h; |
4-propylbenzoyl chloride
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
With tributyl-amine; hydrogen; palladium on activated charcoal In benzene for 6h; Ambient temperature; |
Propylbenzene
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aq. HCl, H3PO4 / acetic acid 2: urotropine / acetic acid View Scheme | |
Multi-step reaction with 2 steps 1: AlCl3 / trichloroethene / 0.5 h / Ambient temperature 2: H2; tributylamine / 10percent Pd/C / benzene / 6 h / Ambient temperature View Scheme |
4-n-propylbenzoic acid
4-n-propylbenzaldehyde
4-bromo-benzaldehyde
isopropyl zinc bromide
A
4-n-propylbenzaldehyde
B
(4-isopropylbenzaldehyde)
Conditions | Yield |
---|---|
With [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride In tetrahydrofuran; toluene at 0 - 20℃; for 3h; Negishi coupling reaction; Inert atmosphere; |
4-propylbenzaldehyde dimethyl acetal
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
With water | 14.6 %Chromat. |
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
With sodium hydride In toluene at 20℃; for 1h; Inert atmosphere; |
Conditions | Yield |
---|---|
With hydrogenchloride; aluminum (III) chloride In hexane at -25 - 13℃; under 21446.5 - 24032.3 Torr; for 2.08333h; Catalytic behavior; Pressure; Temperature; Solvent; Reagent/catalyst; Gatterman-Koch Carbonylation; Autoclave; Sealed tube; | 96.4 %Spectr. |
p-n-propyltoluene
A
4'-methylpropiophenone
B
4-n-propylbenzaldehyde
C
ethyl 4-formylphenyl ketone
Conditions | Yield |
---|---|
With N-hydroxyphthalimide; oxygen; cobalt(II) diacetate tetrahydrate at 20℃; under 760.051 Torr; |
2,4,6-Trinitrotoluene
A
5-hydroxymethyl-2-furfuraldehyde
B
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
With culture of Trichoderma viride |
cis, trans-1,3-dimethylaminocyclohexane
4-n-propylbenzaldehyde
C28H38N2
Conditions | Yield |
---|---|
In methanol at 20℃; Molecular sieve; | 100% |
In methanol at 20℃; Molecular sieve; |
Conditions | Yield |
---|---|
With poly(4-vinylpyridine)/AlPO4-11 In water at 20℃; Knoevenagel condensation; | 98% |
With porous hierarchical MgO/Mg(OH)2 In water at 60℃; for 0.0833333h; Knoevenagel Condensation; | 94% |
Ethyl bromodifluoroacetate
4-n-propylbenzaldehyde
ethyl 2,2-difluoro-3-hydroxy-3-(4-propylphenyl)propanoate
Conditions | Yield |
---|---|
Stage #1: Ethyl bromodifluoroacetate With zinc In tetrahydrofuran at 0℃; for 1h; Inert atmosphere; Stage #2: 4-n-propylbenzaldehyde In tetrahydrofuran for 4h; Inert atmosphere; Reflux; | 97.8% |
diethoxyphosphoryl-acetic acid ethyl ester
4-n-propylbenzaldehyde
ethyl 3-(4-propylphenyl)propionate
Conditions | Yield |
---|---|
Stage #1: diethoxyphosphoryl-acetic acid ethyl ester; 4-n-propylbenzaldehyde With sodium ethanolate In ethanol; toluene at 0 - 25℃; for 4h; Stage #2: With palladium on activated charcoal; hydrogen In isopropyl alcohol at 20℃; | 95.5% |
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
With perchloric acid In ethanol at 20℃; for 0.5h; | 94% |
malonic acid
4-n-propylbenzaldehyde
(E)-3-(4-n-propylphenyl)acrylic acid
Conditions | Yield |
---|---|
Stage #1: malonic acid; 4-n-propylbenzaldehyde With piperidine; pyridine Knoevenagel-Doebner reaction; Reflux; Stage #2: With hydrogenchloride In water Cooling with ice; optical yield given as %de; | 92% |
With piperidine In pyridine at 120℃; for 4h; | |
With piperidine In pyridine | |
In pyridine at 80℃; for 2h; |
Conditions | Yield |
---|---|
With beta zeolite modified with chlorosulphonic acid (28 wtpercent) at 20℃; Neat (no solvent); | 86% |
Conditions | Yield |
---|---|
With ammonium acetate In neat (no solvent) at 60℃; for 0.5h; Green chemistry; | 86% |
1-phenylmethyl-4-piperidone
4-n-propylbenzaldehyde
1-benzyl-3,5-bis(4-propylbenzylidene)piperidin-4-one
Conditions | Yield |
---|---|
With hydrogenchloride In ethanol; water at 0℃; for 6h; Claisen-Schmidt Condensation; Reflux; | 83% |
2-Acetylthiophene
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
With sodiumsulfide nonahydrate In methanol at 20℃; | 83% |
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
With sodium acetate; acetic acid for 24h; Knoevenagel Condensation; Reflux; | 82% |
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In water for 0.2h; Knoevenagel condensation; Reflux; | 81% |
4-n-propylbenzaldehyde
4-n-propylbenzyl alcohol
Conditions | Yield |
---|---|
With sodium tetrahydroborate In tetrahydrofuran at 0℃; for 2h; | 80% |
With sodium hydroxide; sodium tetrahydroborate In methanol; water for 0.583333h; Ambient temperature; | |
With sodium tetrahydroborate; water In acetonitrile |
4-n-propylbenzaldehyde
toluene-4-sulfonic acid hydrazide
Conditions | Yield |
---|---|
In methanol for 0.25h; | 80% |
4-n-propylbenzaldehyde
2-{2-[(methylamino)methyl]-1H-benzimidazol-1-yl}acetohydrazide
N'-[(E)-(4-propylphenyl)methylidene]-2-{2-[(methylamino)methyl]-1H-benzimidazol-1-yl}acetohydrazide
Conditions | Yield |
---|---|
With acetic acid In methanol Reflux; | 80% |
4-n-propylbenzaldehyde
1,3-diaminoguanidine hydrochloride
Conditions | Yield |
---|---|
In ethanol at 100℃; for 0.166667h; Microwave irradiation; | 77% |
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
With sodium methylate; acetic acid for 24h; Reflux; | 77% |
1-(2-furyl)-1-ethanone
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
With sodiumsulfide nonahydrate In methanol at 20℃; | 76% |
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
Stage #1: (E)-(4-(3-oxo-3-phenylprop-1-en-1-yl) benzyl)triphenylphosphonium bromide With sodium hydroxide In dichloromethane at 0℃; for 0.166667h; Wittig Olefination; Stage #2: 4-n-propylbenzaldehyde In dichloromethane Wittig Olefination; | 75% |
4-n-propylbenzaldehyde
trans-1,4-cyclohexyldiamine
Conditions | Yield |
---|---|
In methanol at 20℃; Molecular sieve; | 73% |
4-n-propylbenzaldehyde
4-Hydroxyacetophenone
Conditions | Yield |
---|---|
Stage #1: 4-n-propylbenzaldehyde; 4-Hydroxyacetophenone With sodium hydroxide In methanol at 20℃; for 0.333333h; Claisen-Schmidt Condensation; Stage #2: In methanol at 20℃; Claisen-Schmidt Condensation; | 73% |
4-n-propylbenzaldehyde
methyl vinyl ketone
1-[4-(propyl)phenyl]-pentane-1,4-dione
Conditions | Yield |
---|---|
With 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; triethylamine at 70℃; under 3102.97 Torr; for 0.25h; Stetter reaction; Microwave irradiation; | 72% |
With 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; triethylamine at 70℃; under 3102.97 Torr; for 0.25h; Stetter reaction; Microwave irradiation; | 63% |
4-n-propylbenzaldehyde
Conditions | Yield |
---|---|
With piperidine In ethanol Knoevenagel Condensation; Reflux; | 71% |
4-n-propylbenzaldehyde
4-aminothymol
Conditions | Yield |
---|---|
In methanol at 30 - 35℃; Inert atmosphere; | 68% |
1-(5-bromo-2-chloropyrimidine-4-yl)hydrazine
4-n-propylbenzaldehyde
2-(4-propylbenzylidene)-1-(5-bromo-2-chloropyrimidin-4-yl)hydrazine
Conditions | Yield |
---|---|
In ethanol for 2h; Reflux; | 68% |
4-n-propylbenzaldehyde
5-(tert-butyl)-4-hydroxy-2-methylaniline
C21H27NO
Conditions | Yield |
---|---|
In methanol at 30 - 35℃; Inert atmosphere; | 65% |
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