Bulk Natural Eugenol oil price,Cas 97-53-0 Appearance: light yellow to yellow liquid. Boiling point: 255 °C. Melting point: -9.2 °C to -9.1 °C. Flash point: 110 °C. Relative density (25 °C /25 °C): 1.063~1.068. Refractiv
Cas:97-53-0
Min.Order:1 Kilogram
Negotiable
Type:Other
inquirySyzygium aromaticum Extract Syzygium Aromaticum are the aromatic dried flower buds of a tree in the family Myrtaceae, Syzygium aromaticum. Syzygium Aromaticum are native to the Maluku islands in Indonesia and used as a spice in cuisines all o
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Min.Order:1 Kilogram
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inquiryItems Standard Result Appearance Light yellow liquid pale yellow liquid Content 99.0%min
Cas:97-53-0
Min.Order:1 Gram
FOB Price: $2.0 / 5.0
Type:Manufacturers
inquiryProduct description: Product Name Eugenol CAS No. 97-53-0 Appearance Colorless to yellowish liquid Assay ≥99% Capacity 200mt/year Application Essence and spice, insecticide a
hebei yanxi chemical co., LTD who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do research and developm
Cas:97-53-0
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inquiryUnique advantages for Eugenol Cas 97-53-0 Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Colorless to light yellow liquid Storage:0-6°C Package:25kg/drum,200kg/drum Appl
Cas:97-53-0
Min.Order:25 Kilogram
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Cas:97-53-0
Min.Order:1 Gram
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inquiry1、Our factory passed ISO 9001, ISO 14001, ISO 22000 system certification; HALAL 、KOSHER、FCC AND FDA certificate are available. We can provide customers with better prices, and the supply is stable. 2、We founded in 2004,10% of the staff have more tha
Cas:97-53-0
Min.Order:1 Kilogram
Negotiable
Type:Manufacturers
inquiryShanghai Seasonsgreen Chemical is a high-tech research and development, production, sale and custom synthesis set in one high-tech chemical products enterprises. Our sales and marketing division is located in Shanghai, serving international pharmaceu
Cas:97-53-0
Min.Order:1 Kilogram
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Type:Manufacturers
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Dayangchem’s 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. DayangChem can provide different quantiti
Cas:97-53-0
Min.Order:100 Gram
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Type:Lab/Research institutions
inquiryOur main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
Name:Eugenol CAS NO: 97-53-0 Grade:Antibacterial, lower blood pressure; It can also be used in perfume flavors and cosmetics flavors and soap flavoring formulations, and can also be used for the blending of food flavors. Product Quality 12 years
Cas:97-53-0
Min.Order:25 Kilogram
FOB Price: $1.0 / 2.0
Type:Other
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Cas:97-53-0
Min.Order:1 Kilogram
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inquiryOur company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O
Cas:97-53-0
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
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Min.Order:10 Gram
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Min.Order:10 Kilogram
Negotiable
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inquiryAppearance:Clear pale yellow to yellow liquid Storage:2-8°C Package:200kg/Drum Application:Eugenol is a flavoring obtained from clove oil and also found in car- nation and cinnamon leaves. it is a stable, light yellow-green liquid of clove odor. i
Cas:97-53-0
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Cas:97-53-0
Min.Order:10 Gram
Negotiable
Type:Other
inquiryCAS.NO: 97-53-0 Molecular Formula:C10H12O2 Molecular Weight: 178.23 Index Standard Result Appearance Colorless
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Min.Order:10 Gram
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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
Cas:97-53-0
Min.Order:500 Kilogram
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Type:Lab/Research institutions
inquiryEugenol Oil Is widely used in scent of fern, set incense can be used as modification agent and agent, with the colored soap flavored. Can be used in many flowers such as roses flavour. Can also be used to spice, combination and Oriental type, em
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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
4-allyl-2-methoxy-1-(methoxymethoxy)benzene
4-allylguaiacol
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In neat (no solvent, solid phase) at 20℃; for 0.583333h; Green chemistry; | 96% |
With p-toluenesulfonic acid monohydrate In dichloromethane Solvent; | 95.5% |
With toluene-4-sulfonic acid In dichloromethane Solvent; | 95.5% |
With bismuth(III) chloride In water; acetonitrile at 50℃; for 1h; chemoselective reaction; | 89% |
2-methoxy-4-(prop-2-en-1-yl)phenyl 4-methylbenzenesulfonate
4-allylguaiacol
Conditions | Yield |
---|---|
With magnesium In methanol for 6h; Ambient temperature; | 95% |
Conditions | Yield |
---|---|
Stage #1: 4-allyl-(1-allyloxy)-2-methoxybenzene With tert.-butyl lithium In diethyl ether; pentane at -78℃; for 2h; Inert atmosphere; Stage #2: With methanol In diethyl ether; pentane at -78℃; Inert atmosphere; | 92% |
With ethylmagnesium chloride; iron(II) chloride In tetrahydrofuran; m-xylene at 20℃; for 1h; | 86% |
Conditions | Yield |
---|---|
With lithium chloride In N,N-dimethyl-aniline at 190℃; for 3h; Reagent/catalyst; Solvent; Temperature; Time; Inert atmosphere; | 90% |
With 2,3-Dimethylaniline at 160℃; |
4-Allyl-1-(1-ethoxy-ethoxy)-2-methoxy-benzene
4-allylguaiacol
Conditions | Yield |
---|---|
With diphosphorus tetraiodide In dichloromethane 0 degC, 25 min and room temp., 5 min; | 90% |
4-allylguaiacol
Conditions | Yield |
---|---|
With diphosphorus tetraiodide In dichloromethane at 0℃; for 0.75h; | 90% |
Conditions | Yield |
---|---|
With methanol; potassium permanganate at 25℃; chemoselective reaction; | 90% |
With aluminium trichloride; potassium iodide In water; acetonitrile at 80℃; for 4h; | 83% |
Conditions | Yield |
---|---|
Suzuki-Miyaura Coupling; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 276 - 300℃; for 0.025h; Irradiation; | 87% |
With boron trifluoride diacetate at 68℃; |
3-[3-methoxy-4-(tert-butyldimethylsiloxy)phenyl]-1-propene
4-allylguaiacol
Conditions | Yield |
---|---|
With sodium tetrachloroaurate(III) dihydrate In methanol at 20℃; for 7h; | 87% |
[2-(4-Allyl-2-methoxy-phenoxymethoxy)-ethyl]-trimethyl-silane
A
formaldehyd
B
4-allylguaiacol
C
ethene
D
trimethylsilyl fluoride
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran at 45℃; for 10h; | A n/a B 85% C n/a D n/a |
Conditions | Yield |
---|---|
at 200℃; for 1.5h; Claisen Rearrangement; | A 10% B 84% |
With 1-butyl-2,3-(trimethylene)imidazolium bistriflylimide at 250℃; for 0.025h; Claisen rearrangement; microwave irradiation; | A 18% B 64% |
With bismuth(lll) trifluoromethanesulfonate In acetonitrile for 0.25h; Claisen rearrangement; Heating; | A n/a B 60% |
Conditions | Yield |
---|---|
Stage #1: 2-methoxy-4-(2-propenyl)phenoxyacetic acid With triethylamine In N,N-dimethyl-formamide; toluene for 3h; Curtius rearrangement; Heating; Stage #2: With potassium hydroxide; glycerol In ethanol; N,N-dimethyl-formamide; toluene for 2h; Heating; Further stages.; | 84% |
4-allylguaiacol
Conditions | Yield |
---|---|
With water; lithium hydroxide In tetrahydrofuran; methanol at 0 - 23℃; for 16h; Inert atmosphere; | 75% |
Conditions | Yield |
---|---|
With caesium carbonate In 2,2,2-trifluoroethanol for 18h; Irradiation; | 73% |
1-<(4-hydroxy-3-methoxy)phenyl>-3-(trimethylsilyl)propan-1-ol
4-allylguaiacol
Conditions | Yield |
---|---|
With borontrifluoride acetic acid In dichloromethane at 25℃; for 0.0833333h; | 60% |
2-(4-(allyloxy)-3-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
A
4-allylguaiacol
B
2-methoxy-4-allyl-1-(allyloxy)benzene
Conditions | Yield |
---|---|
With C14H16N6; palladium diacetate; calcium hydroxide In N,N-dimethyl acetamide; water at 50℃; for 24h; Inert atmosphere; | A 57% B 20% |
(E)-2-methoxy-4-(1-propenyl)phenol
A
4-allylguaiacol
B
(+)-licarin A
C
coniferal alcohol
D
vanillin
Conditions | Yield |
---|---|
With Pseudomonas putida NCIM 2176 for 144h; Microbiological reaction; Enzymatic reaction; | A 3% B 16% C 10% D 24% |
methyl magnesium iodide
1,2-dimethoxy-4-(2-propenyl)benzene
A
4-allylguaiacol
B
chavibetol
Conditions | Yield |
---|---|
With diethyl ether; xylene Erhitzen des vom Aether befreiten Reaktionsgemisches auf 160-180grad; |
2-hydroxy-3-methoxy-5-(2-propeny)benzoic acid, methyl ester
aniline
4-allylguaiacol
pyrrolidine
eugenol acetate
A
N-(acetyl)pyrrolidine
B
4-allylguaiacol
Conditions | Yield |
---|---|
for 0.05h; Ambient temperature; |
O-allyl guaiacol
A
2,3-Dihydro-7-methoxy-2-methylbenzofuran
B
4-allylguaiacol
C
6-allylguaicol
Conditions | Yield |
---|---|
With Y-zeolite 1.) n-pentane, r.t., 24 h, 2.) microwave irradiation, 5 min; Yield given. Multistep reaction. Yields of byproduct given; |
1-<(3-methylbut-2-enyl)oxyl>-2-methoxy-4-(2-propenyl)benzene
A
4-allylguaiacol
B
4-allyl-2-methoxy-6-(3-methyl-2-butenyl)phenyl
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 190 - 200℃; for 4h; | A 70 mg B 25 mg |
2-methoxy-4-(2-propenylidene)-2,5-cyclohexadien-1-one, Z-isomer
4-allylguaiacol
2-methoxy-4-(2-propenylidene)-2,5-cyclohexadien-1-one, Z-isomer
A
4-allylguaiacol
B
(E)-2-methoxy-4-(1-propenyl)phenol
Conditions | Yield |
---|---|
With sodium tetrahydroborate In methanol; tetrachloromethane Ambient temperature; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
4-allylguaiacol
Conditions | Yield |
---|---|
With aniline |
tetrachloromethane
diethyl ether
1,2-dimethoxy-4-(2-propenyl)benzene
A
4-allylguaiacol
B
chavibetol
Conditions | Yield |
---|---|
Erhitzen des vom Aether befreiten Reaktionsgemisches auf 160-180grad; |
Conditions | Yield |
---|---|
With hydrogen In 2,2,4-trimethylpentane at 180℃; under 7500.75 - 37503.8 Torr; for 0.166667h; Inert atmosphere; | 100% |
With 4,4'-di-tert-butylbiphenyl; lithium; isopropyl alcohol; nickel dichloride In tetrahydrofuran at 20 - 76℃; Inert atmosphere; chemoselective reaction; | 99% |
With hydrogen In dodecane at 200℃; under 15001.5 Torr; for 1.5h; | 99.1% |
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 20℃; for 24h; Inert atmosphere; | 100% |
With sodium acetate at 130℃; for 0.0111111h; Microwave irradiation; | 98% |
With triethylamine In dichloromethane at 0 - 20℃; for 2h; | 98% |
Conditions | Yield |
---|---|
Stage #1: 4-allylguaiacol With sodium hydride In N,N-dimethyl-formamide at 0℃; for 0.5h; Stage #2: benzyl bromide In N,N-dimethyl-formamide at 0℃; for 1h; | 100% |
With tetra-(n-butyl)ammonium iodide; potassium carbonate In N,N-dimethyl-formamide at 20 - 55℃; Inert atmosphere; | 99% |
With potassium carbonate In acetonitrile at 20℃; for 4h; | 98% |
Conditions | Yield |
---|---|
Stage #1: methanol; 4-allylguaiacol With [bis(acetoxy)iodo]benzene; sodium hydrogencarbonate In benzene at 0℃; for 0.166667h; Stage #2: acenaphthylene In benzene at 20℃; for 22h; Diels-Alder reaction; stereoselective reaction; | 100% |
4-allylguaiacol
4-n-propylcyclohexanol
Conditions | Yield |
---|---|
With hydrogen In dodecane at 200℃; under 15001.5 Torr; for 1.5h; | 99.9% |
Conditions | Yield |
---|---|
With rhodium(III) chloride; ethanol at 140 - 145℃; | 99% |
With tris(triphenylphosphine)ruthenium(II) chloride at 50 - 60℃; for 4h; Temperature; | 99% |
tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; polydimethylsiloxane In methanol; water at 100℃; for 20h; | 82% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 60℃; for 12h; | 99% |
With sodium hydroxide In water; acetone for 8h; Reflux; | 96% |
Stage #1: 4-allylguaiacol With potassium hydroxide In ethanol Stage #2: With sodium carbonate In ethanol Reflux; Stage #3: allyl bromide In ethanol Reflux; | 94% |
4-allylguaiacol
(2-trimethylethylsilylethoxy)methyl chloride
[2-(4-Allyl-2-methoxy-phenoxymethoxy)-ethyl]-trimethyl-silane
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane for 24h; Ambient temperature; | 99% |
Conditions | Yield |
---|---|
With pyridine; aluminium(III) iodide In acetonitrile at 80℃; for 18h; Reagent/catalyst; Solvent; | 99% |
Stage #1: 4-allylguaiacol With pyridine; iodine; aluminium In acetonitrile for 18h; Reflux; Stage #2: With hydrogenchloride In water; acetonitrile at 20℃; Reagent/catalyst; | 99% |
With aluminium(III) iodide; diisopropyl-carbodiimide In acetonitrile at 80℃; for 18h; Reagent/catalyst; | 99% |
Conditions | Yield |
---|---|
With Grotjahn’s catalyst In [(2)H6]acetone at 25℃; for 0.0666667h; Reagent/catalyst; Temperature; Solvent; Inert atmosphere; Glovebox; stereoselective reaction; | 99% |
With platinum(II) chloride In methanol | 96% |
With Grotjahn’s catalyst at 20℃; for 0.333333h; Catalytic behavior; Reagent/catalyst; Glovebox; Inert atmosphere; Green chemistry; diastereoselective reaction; | 95.9% |
4-allylguaiacol
(Ti(C5(CH3)5)Cl2(O(C6H3(OCH3)(CH2CHCH2))))
Conditions | Yield |
---|---|
In toluene Ar atm., room temp.; | 99% |
Conditions | Yield |
---|---|
In tetrahydrofuran Ar atm.; | 99% |
triethylsilane
4-allylguaiacol
((4-allyl-1,2-phenylene)bis(oxy))bis(triethylsilane)
Conditions | Yield |
---|---|
With tris(pentafluorophenyl)borate at 20℃; for 3h; Inert atmosphere; | 99% |
With tris(pentafluorophenyl)borate for 16h; Inert atmosphere; | 99% |
With tris(pentafluorophenyl)borate at 20℃; for 0.166667h; | 99% |
Conditions | Yield |
---|---|
With palladium diacetate; triphenylphosphine; benzoic acid In tetrahydrofuran at -40 - 80℃; under 15001.5 Torr; Autoclave; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
platinum-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In toluene at 80 - 120℃; for 2h; | 98.7% |
Conditions | Yield |
---|---|
With 5%-palladium/activated carbon; potassium carbonate; triphenylphosphine In water at 85 - 105℃; for 16h; Inert atmosphere; | 98.5% |
With bis(η3-allyl-μ-chloropalladium(II)); potassium carbonate; bis[2-(diphenylphosphino)phenyl] ether In water; toluene at 45℃; for 24h; Tsuji-Trost Allylation; Schlenk technique; Inert atmosphere; Sealed tube; | 77% |
Conditions | Yield |
---|---|
Stage #1: 4-allylguaiacol With ammonium hydroxide In water; acetone for 0.166667h; Stage #2: With potassium hexacyanoferrate(III) In water; acetone | 98% |
With ammonium hydroxide; air; potassium hexacyanoferrate(III) In water; acetone at 20℃; | 95% |
With ammonium hydroxide; potassium hexacyanoferrate(III) at 20℃; | 95% |
4-allylguaiacol
Conditions | Yield |
---|---|
With ammonium hydroxide; KFe(CN)6 In acetone | 98% |
Conditions | Yield |
---|---|
Stage #1: 4-allylguaiacol With ozone In ethanol at -55℃; Stage #2: With sodium tetrahydroborate In ethyl acetate at 20℃; | 98% |
Multi-step reaction with 2 steps 1: ozone / sodium hydrogencarbonate / dichloromethane; methanol / 2 h / -78 °C 2: sodium tetrahydroborate; methanol / dichloromethane / 2 h / -78 - 20 °C / Inert atmosphere View Scheme |
4-allylguaiacol
phenylacetyl chloride
phenylacetic acid 4-allyl-2-methoxy-phenyl ester
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 2h; Reflux; | 98% |
With potassium carbonate In acetone for 2h; Reflux; |
Conditions | Yield |
---|---|
With 2-hydroxy-2-methylpropiophenone In 1,4-dioxane; ethanol at 20℃; for 50h; UV-irradiation; | 98% |
With benzoin dimethyl ether at 20℃; for 1h; UV-irradiation; |
Conditions | Yield |
---|---|
With (2-hydroxy-1-[4-(2-hydroxyethoxy)phenyl]-2-methyl-1-propanone) In 1,4-dioxane; ethanol at 100℃; for 0.5h; UV-irradiation; | 98% |
Conditions | Yield |
---|---|
for 4h; Reflux; | 98% |
4-allylguaiacol
prenyl bromide
1-<(3-methylbut-2-enyl)oxyl>-2-methoxy-4-(2-propenyl)benzene
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 60℃; for 12h; | 98% |
Conditions | Yield |
---|---|
With benzoin monomethyl ether In 1,4-dioxane; ethanol at 30℃; for 2h; Reagent/catalyst; Irradiation; | 97.5% |
With 2,2-bis(hydroxymethyl)propionic acid UV-irradiation; |
4-allylguaiacol
Conditions | Yield |
---|---|
With triethylamine; trichlorophosphate In ethyl acetate at 0 - 20℃; for 16.5h; | 97% |
With triethylamine; trichlorophosphate In ethyl acetate at 0 - 20℃; for 24h; | 97% |
With sodium hydroxide; trichlorophosphate extrahieren mit Aether; | |
Stage #1: 4-allylguaiacol With trichlorophosphate In dichloromethane at 0℃; for 4h; Stage #2: With sodium hydroxide In dichloromethane; water Temperature; Reagent/catalyst; Solvent; |
4-allylguaiacol
4-methoxy-benzoyl chloride
4'-allyl-2'-methoxyphenyl 4-methoxybenzoate
Conditions | Yield |
---|---|
Stage #1: 4-allylguaiacol With triethylamine In dichloromethane at 0℃; for 0.5h; Inert atmosphere; Stage #2: 4-methoxy-benzoyl chloride In dichloromethane at 0 - 20℃; for 24.75h; Inert atmosphere; | 97% |
With sodium hydroxide In water at 20℃; for 0.5h; | 85% |
With sodium hydroxide In water at 20℃; for 0.5h; | 43% |
With sodium hydroxide In water at 20℃; for 0.5h; |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide for 25h; | 97% |
4-allylguaiacol
1,1,3,3-Tetramethyldisiloxane
1,3-bis-[3-(4-hydroxy-3-methoxyphenyl)propyl]tetramethyldisiloxane
Conditions | Yield |
---|---|
With dihydrogen hexachloroplatinate In isopropyl alcohol at 60℃; for 4h; | 97% |
Conditions | Yield |
---|---|
With 2-benzyl-2-(dimethylamino)-1-(4-morpholinophenyl)-butan 1-one In 1,4-dioxane; ethanol at 80℃; for 10h; UV-irradiation; | 97% |
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