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Cas:101-86-0
Min.Order:1 Kilogram
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inquiryProduct Name Hexyl cinnamic aldehyde CAS 101-86-0 EINECS 202-983-3 Apparence Light Yellow Liquid Content 97%/99% Applica
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Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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inquiryAbout Our Group Since 1996 when our factory was put into production to year of 2020, our group has successively invested in more than 52 factories with shares and subordinates.We focus on manufacture Pharm & c
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Min.Order:1 Gram
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Min.Order:1 Kilogram
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Min.Order:10 Kilogram
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Min.Order:1 Kilogram
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inquirySuperior quality, moderate price & quick delivery. Appearance:Light 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:Solvent ex
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Min.Order:1 Kilogram
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Min.Order:1 Gram
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Cas:101-86-0
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Negotiable
Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
With benzoic acid; L-proline In neat (no solvent) at 125℃; for 1h; Aldol Condensation; Inert atmosphere; | 97% |
With nitrogen; potassium hydroxide In methanol; water at 30℃; for 6h; | 93.8% |
With pyrrolidine In neat (no solvent) at 120℃; for 0.25h; Microwave irradiation; | 90% |
Octanal
benzaldehyde
A
2-hexyl-2-decenal
B
α-hexylcinnamaldehyde
Conditions | Yield |
---|---|
With p-toluene sulfonic acid impregnated on MCM-41 In neat (no solvent) at 125℃; for 13h; Inert atmosphere; Green chemistry; |
α-hexylcinnamaldehyde
α-hexylcinnamyl alcohol
Conditions | Yield |
---|---|
With tricarbonyl(η4-1,3-bis(trimethylsilyl)-4,5,6,7-tetrahydro-2H-inden-2-one)iron; hydrogen; potassium carbonate In water; isopropyl alcohol at 100℃; under 22502.3 Torr; for 17h; Inert atmosphere; | 98% |
With Cp*Ir(6,6'-dionato-2,2'-bipyridine)(H2O); isopropyl alcohol at 82℃; for 6h; Inert atmosphere; Schlenk technique; chemoselective reaction; | 96% |
With Cp*Ir(6,6'-dionato-2,2'-bipyridine)(H2O); isopropyl alcohol at 82℃; for 6h; Inert atmosphere; Green chemistry; | 96% |
α-hexylcinnamaldehyde
(±)-2-benzyl-1-octanol
Conditions | Yield |
---|---|
With sodium tetrahydroborate; palladium diacetate In methanol at 20℃; for 1h; | 95% |
Conditions | Yield |
---|---|
With bismuth (III) nitrate pentahydrate In ethanol at 100℃; for 12h; Temperature; | 92% |
α-hexylcinnamaldehyde
Conditions | Yield |
---|---|
With 2-pentafluorophenyl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate; water-d2; potassium acetate In dichloromethane at 50℃; for 12h; | 92% |
α-hexylcinnamaldehyde
A
(±)-2-benzyl-1-octanol
B
trans-α-n-hexylcinnamic alcohol
Conditions | Yield |
---|---|
With chlorine[2-(4,5-dihydro-1H-imidazol-2-yl)-6-methoxypyridine](pentamethylcyclopentadienyl)iridium(III) chloride; sodium formate In water at 80℃; for 0.5h; Schlenk technique; chemoselective reaction; | A 91% B n/a |
α-hexylcinnamaldehyde
anthranilic acid amide
Conditions | Yield |
---|---|
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)] In toluene at 120℃; for 12h; Inert atmosphere; | 88% |
Conditions | Yield |
---|---|
With copper(II) bis(trifluoromethanesulfonate) In toluene at 70℃; for 6h; Schlenk technique; Inert atmosphere; | 84% |
Conditions | Yield |
---|---|
With potassium hydroxide at 20℃; | 84% |
α-hexylcinnamaldehyde
N-benzyloxy-α-methyl-α-bromopropionamide
Conditions | Yield |
---|---|
With potassium carbonate at 20℃; | 84% |
α-hexylcinnamaldehyde
toluene-4-sulfonamide
N-(2-hexyl-1H-inden-1-yl)-4-methylbenzenesulfonamide
Conditions | Yield |
---|---|
With aluminum (III) chloride In nitromethane at 80℃; for 6h; | 75% |
Conditions | Yield |
---|---|
With [(C6H6)(PCy3)(CO)RuH]+*BF4−; potassium carbonate; triphenylphosphine In chlorobenzene at 120℃; for 16h; Schlenk technique; regioselective reaction; | 72% |
Conditions | Yield |
---|---|
In ethanol at 60 - 70℃; for 8h; | 69% |
α-hexylcinnamaldehyde
anthranilic acid amide
Conditions | Yield |
---|---|
With bismuth (III) nitrate pentahydrate In ethanol at 100℃; for 12h; | 68% |
Conditions | Yield |
---|---|
With [(C6H6)(PCy3)(CO)RuH]+*BF4−; potassium carbonate; triphenylphosphine In chlorobenzene at 130℃; for 16h; Schlenk technique; regioselective reaction; | 63% |
Conditions | Yield |
---|---|
at -10℃; for 12h; | 60% |
Conditions | Yield |
---|---|
With [(C6H6)(PCy3)(CO)RuH]+*BF4−; potassium carbonate; triphenylphosphine In chlorobenzene at 130℃; for 12h; Schlenk technique; regioselective reaction; | 59% |
Conditions | Yield |
---|---|
In ethanol at 60 - 70℃; for 8h; | 30% |
Conditions | Yield |
---|---|
With sodium hydroxide at 100℃; |
1,5-dimethylhexylamine
α-hexylcinnamaldehyde
(1,5-Dimethyl-hexyl)-[2-[1-phenyl-meth-(E)-ylidene]-oct-(E)-ylidene]-amine
α-hexylcinnamaldehyde
allyl bromide
1-Phenyl-2-hexyl-1,5-hexadien-3-ol
Conditions | Yield |
---|---|
With bismuth 1) DMF, r.t., 4 h, 2) r.t., 3 h; Yield given. Multistep reaction; | |
With bismuth 1.) DMF, room temperature, 2 h, 2.) DMF, room temperature, 2 h; Yield given. Multistep reaction; |
α-hexylcinnamaldehyde
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: NaOH / 100 °C View Scheme |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; magnesium In tetrahydrofuran; (2S)-N-methyl-1-phenylpropan-2-amine hydrate; water |
α-hexylcinnamaldehyde
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 12 h / -10 °C 2: bis(acetylacetonate)oxidovanadium(IV); tert.-butylhydroperoxide / dichloromethane / 2 h / 0 °C View Scheme |
α-hexylcinnamaldehyde
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 12 h / -10 °C 2: bis(acetylacetonate)oxidovanadium(IV); tert.-butylhydroperoxide / dichloromethane / 0 °C View Scheme |
α-hexylcinnamaldehyde
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 12 h / -10 °C 2: bis(acetylacetonate)oxidovanadium(IV); tert.-butylhydroperoxide / dichloromethane / 2 h / 0 °C 3: sodium hydroxide; dihydrogen peroxide / tetrahydrofuran / 0 °C View Scheme |
α-hexylcinnamaldehyde
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 12 h / -10 °C 2: bis(acetylacetonate)oxidovanadium(IV); tert.-butylhydroperoxide / dichloromethane / 2 h / 0 °C 3: sodium hydroxide; dihydrogen peroxide / tetrahydrofuran / 0 °C 4: boron trifluoride diethyl etherate / tetrahydrofuran / 20 °C View Scheme |
Conditions | Yield |
---|---|
With C24H41FFeNP3 In tetrahydrofuran at 60℃; for 7h; Inert atmosphere; Schlenk technique; | |
With C18H37F5FeP4 In tetrahydrofuran at 40℃; Schlenk technique; Inert atmosphere; | |
With o-Ph2P(C6H4)Si(Me)2Fe(H)(PMe3)3 In tetrahydrofuran at 50℃; for 4h; Schlenk technique; | |
With 2C4H8O*C42H47FeOP5 In tetrahydrofuran at 60℃; for 36h; Inert atmosphere; Schlenk technique; |
α-hexylcinnamaldehyde
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: triphenylphosphine / dichloromethane / 0.17 h / 0 °C 1.2: 1 h / 0 °C 2.1: n-butyllithium / tetrahydrofuran; cyclohexane / 1 h / -78 °C 3.1: n-butyllithium / tetrahydrofuran / -78 - 20 °C 4.1: potassium carbonate; gold(I) chloride / 1,2-dichloro-ethane / 60 °C View Scheme |
α-hexylcinnamaldehyde
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: triphenylphosphine / dichloromethane / 0.17 h / 0 °C 1.2: 1 h / 0 °C 2.1: n-butyllithium / tetrahydrofuran; cyclohexane / 1 h / -78 °C 3.1: n-butyllithium / tetrahydrofuran / -78 - 20 °C 4.1: potassium carbonate; gold(I) chloride / 1,2-dichloro-ethane / 60 °C View Scheme |
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