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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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inquiryAcmec is a leading manufacturer and supplier of biochemical reagents and life science products. We have over 40,000 items in stock (real-time inventory) and offer discounted prices to registered members of the online store ( www.acmec.com.cn ) Appea
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inquiry5,6-Dimethylxantheonone-4-acetic acid Application:5,6-Dimethylxantheonone-4-acetic acid
Factory supply high purity low priceAppearance:solid or liquid Storage:sealed in cool and dry place Package:As customer's requested Application:Pharma Intermediate Transportation:by courier/air/sea Port:Any port in China
2-(7-bromo-5,6-dimethyl-9-oxo-9H-xanthene-4-yl) acetic acid
vadimezan
Conditions | Yield |
---|---|
With palladium on activated charcoal; hydrogen | 99% |
With palladium on activated charcoal; hydrogen In methanol under 760.051 Torr; | 85% |
2-<2-(carboxymethyl)phenoxy>-3,4-dimethylbenzoic acid
vadimezan
Conditions | Yield |
---|---|
With sulfuric acid In water at 80℃; for 0.166667h; | 95% |
With sulfuric acid In water at 80℃; for 0.166667h; | 70% |
With sulfuric acid In water for 2h; Heating; | 64.4% |
Conditions | Yield |
---|---|
With potassium phosphate; triphenylphosphine; copper dichloride In toluene at 110℃; for 24h; Reagent/catalyst; | 83% |
ethyl 2-(5,6-dimethyl-9-oxo-9H-xanthen-4-yl)acetate
vadimezan
Conditions | Yield |
---|---|
With water; sodium hydroxide In methanol at 40℃; Darkness; | 75% |
Stage #1: ethyl 2-(5,6-dimethyl-9-oxo-9H-xanthen-4-yl)acetate With water; sodium hydroxide at 40℃; Darkness; Stage #2: With acetic acid In water Darkness; |
(2-hydroxyphenyl)acetic acid disodium salt
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 71 percent / tris[2-(2-methoxyethoxy)ethyl]amine; CuCl / dimethylformamide / 4 h / 85 °C 2: 87 g / H2SO4 / H2O / 0.92 h / 90 °C View Scheme |
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 71 percent / tris[2-(2-methoxyethoxy)ethyl]amine; CuCl / dimethylformamide / 4 h / 85 °C 2: 87 g / H2SO4 / H2O / 0.92 h / 90 °C View Scheme |
6,7-dimethylisatin
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 65 percent / KOH, KCl, 27percent H2O2 / 20 °C 2: 1.) concd. H2SO4, NaNO2, 2.) KI / 1.) water, 10 deg C, 2.) 100 deg C 3: 63 percent / tris<2-(2-methoxyethoxy)ethyl>amine (TDA-1), CuCl / dimethylsulfoxide / 12 h / 95 °C 4: 70 percent / concd. H2SO4 / H2O / 0.17 h / 80 °C View Scheme |
2,3-dimethyl-α-isonitrosoacetanilide
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: 65 percent / CH3SO3H / 70 - 80 °C 2: 65 percent / KOH, KCl, 27percent H2O2 / 20 °C 3: 1.) concd. H2SO4, NaNO2, 2.) KI / 1.) water, 10 deg C, 2.) 100 deg C 4: 63 percent / tris<2-(2-methoxyethoxy)ethyl>amine (TDA-1), CuCl / dimethylsulfoxide / 12 h / 95 °C 5: 70 percent / concd. H2SO4 / H2O / 0.17 h / 80 °C View Scheme |
2-amino-3,4-dimethylbenzoic acid
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 1.) concd. H2SO4, NaNO2, 2.) KI / 1.) water, 10 deg C, 2.) 100 deg C 2: 63 percent / tris<2-(2-methoxyethoxy)ethyl>amine (TDA-1), CuCl / dimethylsulfoxide / 12 h / 95 °C 3: 70 percent / concd. H2SO4 / H2O / 0.17 h / 80 °C View Scheme |
3,4-dimethyl-2-iodobenzoic acid
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 63 percent / tris<2-(2-methoxyethoxy)ethyl>amine (TDA-1), CuCl / dimethylsulfoxide / 12 h / 95 °C 2: 70 percent / concd. H2SO4 / H2O / 0.17 h / 80 °C View Scheme |
2,3-Dimethylaniline
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1: Na2SO4, hydroxylamine sulfate, concd. HCl / H2O 2: 65 percent / CH3SO3H / 70 - 80 °C 3: 65 percent / KOH, KCl, 27percent H2O2 / 20 °C 4: 1.) concd. H2SO4, NaNO2, 2.) KI / 1.) water, 10 deg C, 2.) 100 deg C 5: 63 percent / tris<2-(2-methoxyethoxy)ethyl>amine (TDA-1), CuCl / dimethylsulfoxide / 12 h / 95 °C 6: 70 percent / concd. H2SO4 / H2O / 0.17 h / 80 °C View Scheme |
2,3-Dimethylphenol
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: sodium / methanol / 12 h / 100 °C 2.1: Tris(3,6-dioxaheptyl)amine; copper(l) chloride / dimethyl sulfoxide / 4 h / 85 °C 2.2: pH 2 - 3 3.1: sulfuric acid / water / 0.5 h / 90 °C 4.1: caesium carbonate / palladium diacetate; 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride / 1,4-dioxane / 24 h / 80 °C 5.1: water; sodium hydroxide / 40 °C / Darkness 5.2: Darkness View Scheme | |
Multi-step reaction with 3 steps 1: potassium phosphate; copper dichloride; triphenylphosphine / toluene / 24 h / 110 °C 2: bis(dibenzylideneacetone)-palladium(0); tri tert-butylphosphoniumtetrafluoroborate; 18-crown-6 ether; potassium phosphate / 12 h / 160 °C / Inert atmosphere 3: sodium hydroxide; water / methanol / 40 °C / Darkness View Scheme |
4-bromo-5,6-dimethylxanthone
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: caesium carbonate / palladium diacetate; 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride / 1,4-dioxane / 24 h / 80 °C 2.1: water; sodium hydroxide / 40 °C / Darkness 2.2: Darkness View Scheme |
3-bromo-2-(2,3-dimethylphenoxy)-benzoic acid
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: sulfuric acid / water / 0.5 h / 90 °C 2.1: caesium carbonate / palladium diacetate; 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride / 1,4-dioxane / 24 h / 80 °C 3.1: water; sodium hydroxide / 40 °C / Darkness 3.2: Darkness View Scheme |
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: Tris(3,6-dioxaheptyl)amine; copper(l) chloride / dimethyl sulfoxide / 4 h / 85 °C 1.2: pH 2 - 3 2.1: sulfuric acid / water / 0.5 h / 90 °C 3.1: caesium carbonate / palladium diacetate; 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride / 1,4-dioxane / 24 h / 80 °C 4.1: water; sodium hydroxide / 40 °C / Darkness 4.2: Darkness View Scheme |
2-iodo-3-bromobenzoic acid
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: potassium hydroxide / water / 12 h / 100 °C 2.1: Tris(3,6-dioxaheptyl)amine; copper(l) chloride / dimethyl sulfoxide / 4 h / 85 °C 2.2: pH 2 - 3 3.1: sulfuric acid / water / 0.5 h / 90 °C 4.1: caesium carbonate / palladium diacetate; 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride / 1,4-dioxane / 24 h / 80 °C 5.1: water; sodium hydroxide / 40 °C / Darkness 5.2: Darkness View Scheme |
sodium 2,3-xylenolate
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: Tris(3,6-dioxaheptyl)amine; copper(l) chloride / dimethyl sulfoxide / 4 h / 85 °C 1.2: pH 2 - 3 2.1: sulfuric acid / water / 0.5 h / 90 °C 3.1: caesium carbonate / palladium diacetate; 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride / 1,4-dioxane / 24 h / 80 °C 4.1: water; sodium hydroxide / 40 °C / Darkness 4.2: Darkness View Scheme |
(2-hydroxyphenyl)acetic acid disodium salt
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: Tris(3,6-dioxaheptyl)amine; copper(l) chloride / dimethyl sulfoxide / 8 h / Heating; Inert atmosphere 2: sulfuric acid / water / 2 h / Heating View Scheme |
3,4-dimethylbenzoic acid
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sulfuric acid; N-Bromosuccinimide / 12 h / 20 °C 2: trichlorophosphate; zinc(II) chloride / 0.67 h / 85 °C / Microwave irradiation 3: hydrogen; palladium on activated charcoal / methanol / 760.05 Torr View Scheme |
2,5-dibromo-3,4-dimethylbenzoic acid
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: trichlorophosphate; zinc(II) chloride / 0.67 h / 85 °C / Microwave irradiation 2: hydrogen; palladium on activated charcoal / methanol / 760.05 Torr View Scheme |
2,3-dichlorobenzylaldehyde
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: potassium phosphate; copper dichloride; triphenylphosphine / toluene / 24 h / 110 °C 2: bis(dibenzylideneacetone)-palladium(0); tri tert-butylphosphoniumtetrafluoroborate; 18-crown-6 ether; potassium phosphate / 12 h / 160 °C / Inert atmosphere 3: sodium hydroxide; water / methanol / 40 °C / Darkness View Scheme |
3,4-dimethylbenzaldehyde
vadimezan
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sulfuric acid; potassium nitrate / 1.5 h / -5 - 0 °C 2: potassium phosphate; copper dichloride; triphenylphosphine / toluene / 24 h / 110 °C View Scheme |
1-Phenylethanol
vadimezan
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 99.4% |
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 98.7% |
methanol
vadimezan
methyl 2-(5,6-dimethyl-9-oxo-9H-xanthen-4-yl)acetate
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 98.6% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In dichloromethane; N,N-dimethyl-formamide at 23℃; for 3h; | 88% |
vadimezan
GlyOEt*HCl
ethyl 2-(2-(5,6-dimethyl-9-oxo-9H-xanthen-4-yl)acetamido)acetate
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 60℃; for 24h; | 96.5% |
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 95.8% |
ethanol
vadimezan
ethyl 2-(5,6-dimethyl-9-oxo-9H-xanthen-4-yl)acetate
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 95.4% |
3-amino-propionic acid ethyl ester
vadimezan
ethyl 3-(2-(5,6-dimethyl-9-oxo-9H-xanthen-4-yl)acetamido)propanoate
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 60℃; for 24h; | 92.4% |
vadimezan
cyclohexanol
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 90.6% |
n-heptan1ol
vadimezan
2-(5,6-dimethylxanthone-4-yl)acetic acid heptyl ester
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 87.8% |
With diphenylammonium trifluoromethanesulfonate In toluene Reflux; | 87.8% |
i-Amyl alcohol
vadimezan
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 87.4% |
8-methyl-1-nonanol
vadimezan
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 87.1% |
vadimezan
benzyl alcohol
2-(5,6-dimethylxanthone-4-yl)acetic acid benzyl ester
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 81.7% |
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 80.6% |
vadimezan
aniline
2-(5,6-dimethyl-9-oxo-9H-xanthen-4-yl)-N-phenylacetamide
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 60℃; for 24h; | 80% |
vadimezan
p-aminoethylbenzoate
4-(2-(5,6-dimethylxanthone-4-yl)acetamido)benzoic acid ethyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 60℃; for 24h; | 79.3% |
4-phenyl-butan-1-ol
vadimezan
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 78.7% |
1-octadecanol
vadimezan
2-(5,6-dimethylxanthone-4-yl)acetic acid octadecyl ester
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 73.7% |
vadimezan
isopropyl alcohol
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 73.4% |
vadimezan
2,2-dideutero-2-(1,2,3,7,8-pentadeutero-9-oxo-5,6-bis(trideuteromethyl)-9H-xanthen-4-yl)acetic acid
Conditions | Yield |
---|---|
Stage #1: vadimezan With [D]-sodium hydroxide; hydrogen; water-d2; platinum on carbon; palladium 10% on activated carbon at 180℃; for 96h; Sealed tube; Stage #2: With hydrogenchloride In water pH=3; | 68% |
1-Heptylamine
vadimezan
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 60℃; for 24h; | 66.4% |
propylamine
vadimezan
2-(5,6-dimethyl-9-oxo-9H-xanthen-4-yl)-N-propylacetamide
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 60℃; for 24h; | 64.9% |
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide Heating; | 64.9% |
vadimezan
m,p-dichloroaniline
N-(3,4-dichlorophenyl)-2-(5,6-dimethyl-9-oxo-9H-xanthen-4-yl)acetamide
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 60℃; for 24h; | 58.6% |
vadimezan
allyl alcohol
2-(5,6-dimethylxanthone-4-yl)acetic acid allyl ester
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene for 2h; Reflux; | 57.7% |
vadimezan
3-chloro-aniline
N-(3-chlorophenyl)-2-(5,6-dimethyl-9-oxo-9H-xanthen-4-yl)acetamide
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 60℃; for 24h; | 55.7% |
vadimezan
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 20℃; for 24h; | 52.4% |
vadimezan
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 20℃; for 24h; | 52.4% |
With dmap; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 20℃; for 24h; | 51.3% |
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