Good price Good quality Appearance:powder Storage:dry condition Package:According to the demand of customer Application:intermediate Transportation:By sea or by air Port:Shanghai Port
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Min.Order:1 Gram
Negotiable
Type:Manufacturers
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inquiryProduct Name: 2,4,6-TRIHYDROXYBENZALDEHYDE Synonyms: 2,4,6-TRIHYDROXYBENZALDEHYDE;2,4,6-trihydroxy-benzaldehyd;Benzaldehyde, 2,4,6-trihydroxy-;formylphloroglucinal;Formylphloroglucinol;PHLOROGLUCINOL ALDEHYDE;PHLOROGLUCINALDEHYDE;PHLOROGLUCINOL
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Min.Order:1 Gram
Negotiable
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inquiry2,4,6-TRIHYDROXYBENZALDEHYDE CAS:487-70-7 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organi
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Min.Order:1 Gram
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inquirysuperior quality Appearance:pale pink crystalline powder 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:Reactant involved in the synthesis of bio
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Min.Order:1 Kilogram
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inquiryJ&H CHEM 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. J&H CHEM has some Manufacturing base in Jia
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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inquiryChemlyte Solutions believe that customers and suppliers deserve much more than what traditional distributors can offer. To grow in today s fast-paced and increasingly competitive market it is essential to be able to quickly adapt to market forces eff
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inquiryfactory?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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inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
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GOLDEN PHARMA CO.,LIMITED.is a professional pharmaceutical company,our team have more than 20years expereince in pharmaceutical production and sales. we are a professional technical enterprise specializing in the R & D, production,QA regulation
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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
1,3,5-Trihydroxybenzene dihydrate
N,N-dimethyl-formamide
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
With trichlorophosphate In ethyl acetate at 20℃; for 1h; Vilsmeier-Haack Formylation; Cooling with ice; | 98% |
3,5-dihydroxyphenol
N,N-dimethyl-formamide
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
Stage #1: 3,5-dihydroxyphenol; N,N-dimethyl-formamide With oxalyl dichloride In acetonitrile at 0℃; for 0.5h; Stage #2: With water at 80℃; for 2h; | 96% |
Stage #1: N,N-dimethyl-formamide With trichlorophosphate at 0 - 25℃; for 0.5h; Vilsmeier-Haack Formylation; Stage #2: 3,5-dihydroxyphenol In 1,4-dioxane at 0 - 25℃; for 3h; Vilsmeier-Haack Formylation; Inert atmosphere; | 95% |
With trichlorophosphate In ethyl acetate at 0 - 20℃; for 2h; Vilsmeier-Haack Formylation; Inert atmosphere; | 92% |
Conditions | Yield |
---|---|
With trichlorophosphate In N,N-dimethyl-formamide at 0 - 20℃; for 4h; Inert atmosphere; | 80% |
With hydrogenchloride; diethyl ether; mercury(II) fulminate Hydroysierung des Oxims; |
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
With water In methanol at 20℃; for 4h; Hydrolysis; | 79.2% |
Conditions | Yield |
---|---|
With hydrogenchloride | |
With hydrogenchloride; diethyl ether; zinc(II) chloride Beim Kochen des Reaktionsprodukts mit Wasser; |
Conditions | Yield |
---|---|
With hydrogenchloride | |
With hydrogenchloride; diethyl ether Erwaermen des ausfallenden salzsauren Aldimids mit Wasser und Schwefelsaeure; |
Conditions | Yield |
---|---|
With diethyl ether; trichlorophosphate und Zerlegen des Reaktionsproduktes mit Wasser; |
3,5-dihydroxyphenol
dichloromethyl-methyl sulfide
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
(i) ZnCl2, Et2O, (ii) aq. HCl; Multistep reaction; |
Conditions | Yield |
---|---|
With sodium hydroxide In water for 1h; Heating; |
Conditions | Yield |
---|---|
With 18-crown-6 ether In tetrahydrofuran; toluene Product distribution; -10 deg C, then room temp.; |
Conditions | Yield |
---|---|
With 18-crown-6 ether In tetrahydrofuran; toluene Product distribution; -10 deg C, then room temp.; |
Conditions | Yield |
---|---|
With 18-crown-6 ether In tetrahydrofuran; toluene Product distribution; -10 deg C, then room temp.; |
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran; hexane |
hydrogenchloride
3,5-dihydroxyphenol
diethyl ether
A
2,4,6-trihydroxybenzaldehyde
B
2,4-diformyl 2,4,6-trihydroxybenzene
Conditions | Yield |
---|---|
Erwaermen des Reaktionsprodukts mit Wasser auf dem Dampfbad; |
Conditions | Yield |
---|---|
With hydrogenchloride; diethyl ether |
3,5-dihydroxyphenol
A
2,4,6-trihydroxybenzaldehyde
B
2,4-diformyl 2,4,6-trihydroxybenzene
Conditions | Yield |
---|---|
With hydrogenchloride; diethyl ether Erwaermen des Reaktionsprodukts mit Wasser; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: POCl3 / 0.33 h / 0 °C 1.2: acetonitrile / 18 h / 20 °C 2.1: 79.2 percent / H2O / methanol / 4 h / 20 °C View Scheme |
myrtillin
A
3,4,5-trihydroxybenzoic acid
B
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
With water at 37℃; pH=7.4; Kinetics; aq. phosphate buffer; |
cyanidin-3-glucoside chloride
A
3,4-Dihydroxybenzoic acid
B
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
With water at 37℃; pH=7.4; Kinetics; aq. phosphate buffer; |
cyanidin chloride
A
3,4-Dihydroxybenzoic acid
B
acide 2,4,6-trihydroxybenzoique
C
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
With hydrogenchloride In ethanol; water at 20℃; pH=4.8; Kinetics; pH-value; |
malvidin 3-O-glucoside
C
3,5-dimethoxy-4-hydroxybenzoic acid
D
2,4,6-trihydroxybenzaldehyde
I
(Z)-1-(4-Hydroxy-3,5-dimethoxy-phenyl)-2-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-3-(2,4,6-trihydroxy-phenyl)-propenone
Conditions | Yield |
---|---|
With water In acetonitrile at 35℃; for 72h; pH=1; |
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-chromen-4-on
A
3,4-Dihydroxybenzoic acid
B
2,4,6-trihydroxybenzaldehyde
D
2-(3',4'-dihydroxybenzoyloxy)-4,6-dihydroxybenzoic acid
G
3',4',5,6,7-pentahydroxyflavone
Conditions | Yield |
---|---|
With oxygen; potassium hydroxide In methanol |
2,4,6-trihydroxybenzaldehyde
acetic anhydride
5,7-diacetoxyl-2-chromenone
Conditions | Yield |
---|---|
With sodium acetate at 190℃; for 14h; | 100% |
Conditions | Yield |
---|---|
With hydrogenchloride; zinc In diethyl ether; ethyl acetate for 0.166667h; Clemmensen Reduction; Cooling with ice; | 99% |
With hydrogenchloride; zinc In diethyl ether; water; ethyl acetate for 0.166667h; Clemmensen Reduction; Cooling with ice; | 99% |
With hydrogenchloride; methyl orange; sodium cyanoborohydride In tetrahydrofuran; water at 20℃; for 12h; pH=4; | 78% |
2,4,6-trihydroxybenzaldehyde
5-amino-1-(4-methoxyphenyl)-1H-imidazole-4-carbonitrile
C18H14N4O4
Conditions | Yield |
---|---|
With trifluoroacetic acid In ethanol at 20℃; | 98% |
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; acetic acid In methanol for 1h; | 98% |
Stage #1: 2,4,6-trihydroxybenzaldehyde With hydrogenchloride; pentane-1,3-diol In 1,4-dioxane; water at 20℃; for 16h; Stage #2: In 1,4-dioxane; n-heptane at 0℃; for 2h; Mechanism; | 41% |
2,4,6-trihydroxybenzaldehyde
ethyl (triphenylphosphoranylidene)acetate
ethyl (2E)-3-(2,4,6-trihydroxyphenyl)arylate
Conditions | Yield |
---|---|
In tetrahydrofuran at 30℃; for 8h; | 97% |
Conditions | Yield |
---|---|
Stage #1: (3,4-Dimethoxyphenyl)acetic acid; 2,4,6-trihydroxybenzaldehyde With acetic anhydride; triethylamine at 112℃; for 1.16667h; Microwave irradiation; Green chemistry; Stage #2: With hydrogenchloride In ethanol; water at 80℃; for 3h; Green chemistry; | 96% |
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
With acetic acid In ethanol | 96% |
5-nitrospiro[1,3-dioxolane-2,3’-indol]-2’(1’H)-one
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
With triethylamine In ethanol for 8h; Reflux; | 95% |
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
With acetic acid In methanol for 3h; Reflux; | 94.1% |
Conditions | Yield |
---|---|
In water at 25℃; for 2h; | 94% |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; | 94% |
Conditions | Yield |
---|---|
In ethanol; water Reflux; | 93.6% |
2,4,6-trihydroxybenzaldehyde
tert-butyldimethylsilyl chloride
2,4,6-tri-tert-butyldimethylsilyloxybenzaldehyde
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; silylation; | 93% |
2-hydrazinoquinoxaline
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
With acetic acid In methanol for 3h; Reflux; | 93% |
Conditions | Yield |
---|---|
With acetic acid In methanol for 3h; Reflux; | 92% |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; | 92% |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; | 92% |
Conditions | Yield |
---|---|
With acetic acid In ethanol Reflux; | 90% |
With acetic acid In ethanol Reflux; | |
With acetic acid In methanol Reflux; |
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; ethyl acetate In methanol at 0 - 20℃; Aldol Condensation; | 90% |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; | 90% |
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
With acetic acid In methanol for 3h; Reflux; | 89.4% |
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
With pyridinium hydrobromide perbromide In tetrahydrofuran at -20℃; for 3h; | 89% |
2,4,6-trihydroxybenzaldehyde
2-(3,5-dihydroxyphenyl)acetic acid
acetic anhydride
5,7-diacetoxy-3-(3',5'-diacetoxyphenyl)coumarin
Conditions | Yield |
---|---|
With triethylamine at 110℃; | 88% |
With triethylamine at 120℃; for 8h; Perkin reaction; regioselective reaction; | 88% |
1-bromo dodecane
2,4,6-trihydroxybenzaldehyde
2,4,6-tris(decyloxy)benzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 110℃; for 48h; | 88% |
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 110℃; for 48h; | 88% |
bromethyl methyl ether
2,4,6-trihydroxybenzaldehyde
2-hydroxy-4,6-bis(methoxymethoxy)benzaldehyde
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trihydroxybenzaldehyde With N-ethyl-N,N-diisopropylamine In dichloromethane at 0℃; Inert atmosphere; Stage #2: bromethyl methyl ether In dichloromethane at 20℃; for 12h; Inert atmosphere; | 88% |
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0℃; for 3.5h; Inert atmosphere; | 76% |
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0℃; for 3.5h; Inert atmosphere; | 76% |
Conditions | Yield |
---|---|
With sodium hydroxide In water Inert atmosphere; Reflux; | 88% |
2-(2-bromo-4-hydroxyphenyl)acetic acid
2,4,6-trihydroxybenzaldehyde
Conditions | Yield |
---|---|
With triethylamine In acetic anhydride at 110℃; for 7h; Temperature; Reagent/catalyst; | 88% |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; | 88% |
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