Unique advantages for Amylcinnamaldehyde Cas 122-40-7 Guaranteed the purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Liquid Storage:2-8°C Package:200kg/drum Application:Food Transportation:
Cas:122-40-7
Min.Order:25 Kilogram
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inquiryhigh quality Appearance:White or off-white Solid Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai
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Cas:122-40-7
Min.Order:1 Gram
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Type:Manufacturers
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Type:Lab/Research institutions
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Min.Order:1 Kilogram
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Type:Trading Company
inquiryHeptanal,2-(phenylmethylene)- FEMA 2061;JASMINAL;A-PENTYLCINNAMALDEHYDE;ACA;A-AMYL CINNAMIC ALDEHYDE;ALPHA-PENTYLCINNAMALDEHYDE;ALPHA-N-AMYLCINNAMALDEHYDE;ALPHA-N-AMYL CINNAMIC ALDEHYDE The properties of methyl permethaldehyde Boiling point 2
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inquiry1. Product advantages ♦ High purity, all above 98.5%, no impurities after dissolution ♦ We will test each batch to ensure quality ♦ OEM and private brand services designed for free ♦ Various cap colors available ♦ W
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inquiryName: Alpha-amyl cinnamic aldehyde Synonyms: alpha-amylcinnamaldehyde, mixture of cis and CAS:122-40-7 MF: C14H18O Appearance: white powder Storage:Store in cool and dry place, away from sun light. Package: 25kgs/drum Application: Flavours & Fr
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Min.Order:1 Metric Ton
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Type:Manufacturers
inquiryAppearance:pale yellow liquid Storage:2-8°C Package:200kg/drum Application:amyl cinnamal is used as a fragrance. Although it is naturally occurring in some plants, it is most often synthetically derived when used in cosmetic products. Transportatio
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Min.Order:1 Kilogram
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Min.Order:1 Kilogram
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Min.Order:10 Gram
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Type:Lab/Research institutions
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Min.Order:1 Gram
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Min.Order:1 Kilogram
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inquiryMinimum Order Qty. 10 Gram Supply Ability 500 Kilograms/Month Storage store in cool, dry, ventilated place 20℃ Delivery Time 3 business days after payment Payment Term TT,western union,Paypal,MoneyGram Package 10g,20g,50g,100g,500g,1KGS,
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Min.Order:10 Gram
Negotiable
Type:Trading Company
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Min.Order:1 Gram
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Type:Lab/Research institutions
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Min.Order:0 Metric Ton
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inquiryGMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,
factory?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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Min.Order:1 Kilogram
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Type:Trading Company
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
Conditions | Yield |
---|---|
With benzoic acid; L-proline In neat (no solvent) at 125℃; for 1h; Reagent/catalyst; Time; Aldol Condensation; Inert atmosphere; | 97% |
With amino-functionalized [Zr6O4(OH)4(O2C-C6H4-CO2)6], UiO-66(NH2) at 159.84℃; for 1h; cross-aldol condensation; chemoselective reaction; | 90% |
With potassium carbonate; N-benzyl-N,N,N-triethylammonium chloride In dichloromethane for 3h; | 80% |
Conditions | Yield |
---|---|
With chitosan/titanium dioxide microspheres In toluene at 80℃; for 4h; Inert atmosphere; | |
With chitosan at 160℃; for 8h; chemoselective reaction; | |
With aluminum oxide In toluene at 120℃; Inert atmosphere; |
Conditions | Yield |
---|---|
With cetyltrimethylammonim bromide; sodium hydroxide In water at 30℃; for 4h; Concentration; |
heptanal
benzaldehyde
A
oenanthic acid
B
jasminaldehyde
C
benzoic acid
Conditions | Yield |
---|---|
With sodium hydroxide In water at 30℃; for 72h; |
heptanal
benzaldehyde
A
(E)-2-n-pentyl-2-n-nonenal
B
jasminaldehyde
Conditions | Yield |
---|---|
With potassium hydroxide; Aliquat 336 at 118℃; for 0.0166667h; Irradiation; | A 18% B 82% |
With calcined-hydrotalcite supported on hexagonal mesoporous silica at 150℃; Mechanism; Kinetics; Aldol condensation; Inert atmosphere; |
Conditions | Yield |
---|---|
at 200℃; |
Conditions | Yield |
---|---|
With 4-dimethylaminopyridine functionalized zirconium-benzene-1,4-dicarboxylate-metal organic framework for 1h; Catalytic behavior; Reagent/catalyst; Aldol Condensation; |
heptanal
benzaldehyde
A
2-pentyl-2-nonenal
B
oenanthic acid
C
jasminaldehyde
Conditions | Yield |
---|---|
With diethylamine for 1h; Catalytic behavior; Reagent/catalyst; Aldol Condensation; |
Conditions | Yield |
---|---|
With formic acid; iron(II) tetrafluoroborate hexahydrate; tris(2-diphenylphosphinoethyl)phosphine In tetrahydrofuran at 60℃; for 2h; Schlenk technique; Inert atmosphere; | 99% |
With iron(II) fluoro{tris[2-(diphenylphosphino)phenyl]phospino}tetrafluoroborate; hydrogen; trifluoroacetic acid In isopropyl alcohol at 120℃; under 15001.5 Torr; Inert atmosphere; Autoclave; chemoselective reaction; | 98% |
With Cp*Ir(6,6'-dionato-2,2'-bipyridine)(H2O); isopropyl alcohol at 82℃; for 6h; Inert atmosphere; Schlenk technique; chemoselective reaction; | 97% |
jasminaldehyde
(±)-2-benzyl-1-heptanol
Conditions | Yield |
---|---|
With sodium tetrahydroborate; palladium diacetate In methanol at 20℃; for 0.5h; | 98% |
jasminaldehyde
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; | 96% |
(1-bromovinyl)triisopropylsilane
jasminaldehyde
(E)-4-benzylidene-2-(triisopropylsilyl)non-1-en-3-ol
Conditions | Yield |
---|---|
Stage #1: (1-bromovinyl)triisopropylsilane With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1h; Inert atmosphere; Stage #2: jasminaldehyde In tetrahydrofuran; hexane at -78℃; Inert atmosphere; | 94% |
2-Diazo-3-oxo-butyric acid methyl ester
t-butyldimethylsiyl triflate
jasminaldehyde
Conditions | Yield |
---|---|
With 2,6-dimethylpyridine; zinc trifluoromethanesulfonate In dichloromethane at -78 - 20℃; Mukaiyama reaction; Inert atmosphere; regioselective reaction; | 92% |
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 92% B n/a |
Conditions | Yield |
---|---|
With iron(III) chloride In acetic acid methyl ester Heating; | 90% |
Conditions | Yield |
---|---|
iron(III) chloride In acetic acid for 3h; Heating / reflux; | 87% |
Conditions | Yield |
---|---|
With copper(II) bis(trifluoromethanesulfonate) In toluene at 70℃; for 6h; Schlenk technique; Inert atmosphere; | 86% |
Conditions | Yield |
---|---|
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)] In toluene at 120℃; for 12h; Inert atmosphere; | 84% |
Conditions | Yield |
---|---|
With palladium on activated charcoal; hydrogen In methanol at 20℃; for 20h; | 75% |
With 5%-palladium/activated carbon; hydrogen; potassium carbonate In methanol at 39.84℃; under 3750.38 Torr; for 0.833333h; Autoclave; chemoselective reaction; | 97.6 %Chromat. |
natural Huperzine A
jasminaldehyde
Conditions | Yield |
---|---|
With triethylamine In methanol at 60℃; | 72.8% |
Conditions | Yield |
---|---|
With acetic acid In ethanol at 20℃; for 0.5h; | 66% |
jasminaldehyde
1,2-diamino-benzene
A
2-hexylbenzimidazole
B
2-phenyl-1H-benzoimidazole
Conditions | Yield |
---|---|
With tetra(n-butyl)ammonium hydroxide; water at 150℃; for 0.166667h; Microwave irradiation; Green chemistry; | A 61% B 50% |
Conditions | Yield |
---|---|
With diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; (4s,6s)-2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile; (2S,4S)-2,4-bis(diphenylphosphino)pentane; N-ethyl-N,N-diisopropylamine; cobalt(II) bromide In tetrahydrofuran at 20℃; for 24h; Irradiation; Inert atmosphere; Schlenk technique; stereoselective reaction; | 10% |
Conditions | Yield |
---|---|
With sodium acetate; acetic anhydride |
Conditions | Yield |
---|---|
With piperidine |
Conditions | Yield |
---|---|
(i) Zn, benzene, ether, (ii) KOH, EtOH; Multistep reaction; |
1,5-dimethylhexylamine
jasminaldehyde
(1,5-Dimethyl-hexyl)-[2-[1-phenyl-meth-(E)-ylidene]-hept-(E)-ylidene]-amine
hydrazinecarbodithioic acid methyl ester
jasminaldehyde
N'-[2-[1-Phenyl-meth-(E)-ylidene]-hept-(E)-ylidene]-hydrazinecarbodithioic acid methyl ester
4-methylbenzene-1,3-diamine
jasminaldehyde
4-Methyl-N1,N3-bis-[2-[1-phenyl-meth-(E)-ylidene]-hept-(E)-ylidene]-benzene-1,3-diamine
Conditions | Yield |
---|---|
In ethanol for 5h; Heating; also ZnCl2, 160 deg C, 0.5 h, 180 deg C, 5 min; |
jasminaldehyde
A
2-methyl-1-phenyl-heptane
Conditions | Yield |
---|---|
With ethanol; palladium Hydrogenation; |
jasminaldehyde
C39H46N2O2S2
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aq. ethanol / 5 h / Heating; also ZnCl2, 160 deg C, 0.5 h, 180 deg C, 5 min 2: 61 percent / benzene / 6 h / Heating View Scheme |
jasminaldehyde
C41H50N2O2S2
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aq. ethanol / 5 h / Heating; also ZnCl2, 160 deg C, 0.5 h, 180 deg C, 5 min 2: 64 percent / benzene / 6 h / Heating View Scheme |
jasminaldehyde
3-Pentyl-4-phenyl-buta-1,3-dien
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: (i) Zn, benzene, ether, (ii) KOH, EtOH 2: 98 °C / 20 Torr / (thermolysis) View Scheme |
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