As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
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inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
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inquiryThe 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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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
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inquiryOur Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con
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inquiryHenan Tianfu Chemical Co., Ltd. is located in Zhengzhou High-tech Development Zone with import and export license. We passed ISO 9001:2008 in 2009, and won "High-tech Enterprise" by provincial government in 2013.The objective of the com
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inquiryOur Advantage: high quality with competitive price High quality standard: BP/USP/EP Enterprise standard All purity customized Fast and safe delivery We have reliable forwarder who can help us deliver our goods more fast and safe. We
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inquiryAbout Product Details
Cas:86-51-1
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inquiryName: 2,3-Dimethoxybenzaldehyde Synonyms: o-veratraldehyde MF: C9H10O3 Appearance:White Powder Storage: Store in cool and dry place, away from sun light. Package:25kg Application: Pharmaceutical Intermediate Transportation:By sea or by air Port:Qi
1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; Appearance:White Crystalline Solid Storage:Store in sealed contai
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inquiryhebei 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 developmen
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inquiry1.No Less 8 years exporting experience. Clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specialized
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Hebei Mojin Biotechnology Co., Ltd, Our company is a professional chemical raw materials and chemical reagents research and development production enterprises. We have several production line,So we can control the lowest price. We also have several
Cas:86-51-1
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inquiryBest quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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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
Massive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and
Cas:86-51-1
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inquiryWe are one of a few suppliers that can offer custom synthesis service of this product We are specialized in custom synthesis, chemical/pharmaceutical/ pesticides outsourcing and contract research. We are committed to prov
Cas:86-51-1
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inquirysuperior quality Appearance:Slightly yellow crystals 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:A benzaldehyde derivative that may possess an
Product name: 2,3-Dimethoxybenzaldehyde CAS No.:86-51-1 Molecule Formula:C9H10O3 Molecule Weight:166.17 Purity: 99% Package: 25kg/drum Description:White crystalline powder Manufacture Standards:Enterprise Standard TESTING ITEMS
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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,
Product Name: 2,3-Dimethoxybenzaldehyde Synonyms: 3,5-Dihydroxypropiophenone;3,5-Dimethylsalicylic acid;LABOTEST-BB LT00932325;BENZALDEHYDE, 2,3-DIMETHOXY-;O-VERATRALDEHYDE;O-VERATRIC ALDEHYDE;4-Diethoxybenzene;2,3-Dimethoxybenzenecarbonal CAS:
Cas:86-51-1
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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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inquiryShandong Mopai Biotechnology Co., LTD is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemicals. W
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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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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
Cangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new api, intermediat
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inquiryConditions | Yield |
---|---|
With aluminium trichloride; 1-decyl-4-aza-1-azoniabicyclo[2.2.2]octane chlorochromate In acetonitrile for 1.4h; Heating; | 99% |
With benzyltriphenylphosphonium dichromate In acetonitrile for 0.333333h; Oxidation; Heating; | 98% |
With benzyltriphenylphosphonium chlorochromate In dichloromethane for 0.0333333h; Oxidation; microwave irradiation; | 98% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 45℃; for 42h; | 99% |
Stage #1: 3-methoxy-2-hydroxybenzaldehyde With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.25h; Stage #2: methyl iodide In N,N-dimethyl-formamide at 20℃; | |
Stage #1: 3-methoxy-2-hydroxybenzaldehyde With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.25h; Stage #2: methyl iodide In N,N-dimethyl-formamide at 20℃; | |
Stage #1: 3-methoxy-2-hydroxybenzaldehyde With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.25h; Stage #2: methyl iodide In N,N-dimethyl-formamide at 20℃; |
3-methoxy-2-hydroxybenzaldehyde
dimethyl sulfate
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate In benzene | 98.7% |
With potassium carbonate In methanol for 2.5h; Heating; | 93% |
With potassium carbonate In benzene for 26h; Heating; | 89% |
Conditions | Yield |
---|---|
With triethylamine; magnesium chloride In 5,5-dimethyl-1,3-cyclohexadiene at 100℃; for 6h; | 94.4% |
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
With bismuth(lll) trifluoromethanesulfonate In dichloromethane; water at 20℃; for 0.166667h; | 90% |
Conditions | Yield |
---|---|
Stage #1: 2,3-dihydroxybenzaldehyde With potassium carbonate In acetone at 20℃; for 0.5h; Stage #2: dimethyl sulfate In acetone at 20℃; for 5h; | 89% |
With sodium hydroxide In water for 1h; Heating; | 68% |
dicobalt octacarbonyl
2,3-dimethoxyphenyl triflate
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
With triethylsilane; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; sodium acetate In acetonitrile at 25℃; for 16h; Schlenk technique; Inert atmosphere; | 83% |
With triethylsilane; potassium acetate; palladium diacetate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene at 50℃; for 12h; Schlenk technique; Inert atmosphere; Molecular sieve; | 72% |
Conditions | Yield |
---|---|
With iodine; triethylamine; triphenylphosphine In toluene at 80℃; for 4h; Sealed tube; | 82% |
1,2-Dimethoxy-3-phenethyloxymethyl-benzene
A
2-phenylethanol
B
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In dichloromethane; water at 20℃; for 12.5h; | A 75% B 73% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 1h; | 73% |
2,3-dihydroxybenzaldehyde
methyl iodide
A
3-hydroxy-2-methoxybenzaldehyde
B
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
Stage #1: 2,3-dihydroxybenzaldehyde With potassium hydrogencarbonate In N,N-dimethyl-formamide for 0.5h; Inert atmosphere; Stage #2: methyl iodide In N,N-dimethyl-formamide at 20℃; for 28h; Inert atmosphere; | A 72% B n/a |
Stage #1: 2,3-dihydroxybenzaldehyde With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: methyl iodide In N,N-dimethyl-formamide at 20℃; for 18h; | A 57% B 19% |
Stage #1: 2,3-dihydroxybenzaldehyde With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: methyl iodide In N,N-dimethyl-formamide at 20℃; for 18h; | A 57% B 19% |
With sodium hydride In dimethyl sulfoxide at 25℃; for 17h; NaH : pyrocatechlol 1.1; Yields of byproduct given; | A 52% B n/a |
4-nitrophenylboronic acid
B
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
With potassium phosphate; water; palladium diacetate; bis[2-(diphenylphosphino)phenyl] ether In toluene at 100℃; for 18h; | A 67% B n/a |
2,3-dihydroxybenzaldehyde
methyl iodide
A
3-methoxy-2-hydroxybenzaldehyde
B
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
With sodium hydride In dimethyl sulfoxide at 25℃; for 17h; NaH : pyrocatechlol 2.2; Yields of byproduct given; | A 58% B n/a |
2-(2,3-dimethoxyphenyl)-2-hydroxyacetonitrile
A
hydrogen cyanide
B
2,3-dimethyoxybenzaldehyde
1,2-dimethoxy-3-((1E)-prop-1-en-1-yl)benzene
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
With potassium dichromate; sulfuric acid; 4-aminobenzene sulfonic acid | |
With potassium dichromate; sulfuric acid | |
With ozone; ethyl acetate at -20℃; und Erhitzen des Reaktionsgemisches mit Wasserdampf; |
3-methoxy-2-hydroxybenzaldehyde
dimethyl sulfate
A
2,3-dimethoxybenzaldehyde dimethylacetal
B
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
With potassium hydroxide |
Conditions | Yield |
---|---|
With Pd-BaSO4; xylene at 140℃; Hydrogenation; |
Conditions | Yield |
---|---|
With oxygen; copper; sodium carbonate; copper(I) chloride 1.) CH3CN; Multistep reaction; |
2,3-dimethoxybenzoic acid
A
2,3-dimethoxybenzyl alcohol
B
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; diisobutylaluminium hydride; triethylamine 1.) CH2Cl2, 0 deg C; 2.) CH2Cl2, -78 deg C; Yield given. Multistep reaction. Yields of byproduct given; |
hydrogenchloride
A
homopiperonylamine hydrochloride
B
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
With alkaline solution |
tetrachloromethane
2,3-dimethoxybenzoyl chloride
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
at 140℃; Hydrogenation; |
Conditions | Yield |
---|---|
With benzene |
2-cyano-3t-(2,3-dimethoxy-phenyl)-acrylic acid
2,3-dimethyoxybenzaldehyde
2-benzyl-3-(2,3-dimethoxyphenyl)-5-propylcarbamoyl-2,3-dihydroisoxazole-4-carboxylic acid methyl ester
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
In tetrahydrofuran Heating; |
C-(2,3-dimethoxyphenyl)-N-benzyl-nitrone
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 73 percent / benzene / 22 h / 20 °C 2: 37 percent / methanol / 3 h / 20 °C 3: tetrahydrofuran / Heating View Scheme |
2-benzyl-3-(2,3-dimethoxyphenyl)-2,3-dihydroisoxazole-4,5-dicarboxylic acid dimethyl ester
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 37 percent / methanol / 3 h / 20 °C 2: tetrahydrofuran / Heating View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 86 percent / BBr3 / CHCl3 / 1. 0 deg C, 2.5 h; 2. room temperature, overnight 2: 68 percent / NaOH / H2O / 1 h / Heating View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: chloroform; phosphorus pentachloride 2: palladium-barium sulfate; xylene / 140 °C / Hydrogenation View Scheme |
methylamine
2,3-dimethyoxybenzaldehyde
(2,3-dimethoxy-benzylidene)-methyl-amine
Conditions | Yield |
---|---|
at 20℃; for 12h; | 100% |
In ethanol at 0 - 40℃; | 90% |
With benzene zuletzt unter Erwaermen und Entfernen des gebildeten Wassers; | |
In benzene for 2h; Reflux; | |
In ethanol; water |
Conditions | Yield |
---|---|
With sodium tetrahydroborate In methanol at 20℃; for 0.166667h; | 100% |
With sodium tetrahydroborate In ethanol for 20h; Ambient temperature; | 99% |
With sodium tetrahydroborate In methanol at 20℃; for 1h; | 99% |
1-Bromotetradecane
2,3-dimethyoxybenzaldehyde
(+/-)-1-hydroxy-1-(2.3-dimethoxy-phenyl)-pentadecane
Conditions | Yield |
---|---|
Stage #1: 1-Bromotetradecane With iodine; magnesium In diethyl ether Stage #2: 2,3-dimethyoxybenzaldehyde In diethyl ether for 4h; Reflux; | 100% |
With lithium In tetrahydrofuran at 0℃; | 63% |
tert-butylisonitrile
acetic acid
1-amino-2-propene
2,3-dimethyoxybenzaldehyde
2-(acetylallylamino)-N-tert-butyl-2-(2,3-dimethoxyphenyl)acetamide
Conditions | Yield |
---|---|
In methanol at 20℃; for 6h; Ugi reaction; | 100% |
(S)-1-Aminoindane
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) Milling; | 100% |
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) Milling; | 100% |
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) Milling; | 100% |
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) Milling; | 100% |
nitromethane
2,3-dimethyoxybenzaldehyde
1,2-Dimethoxy-3-((E)-2-nitro-vinyl)-benzene
Conditions | Yield |
---|---|
With ammonium acetate; acetic acid at 22℃; for 3h; ultrasound; | 99% |
81% | |
With sodium hydroxide In methanol; water for 0.5h; Cooling with ice; | 46% |
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
With potassium tert-butylate In tetrahydrofuran at 0 - 20℃; for 16h; Wittig reaction; | 99% |
Stage #1: (2-iodo-4,5-dimethoxybenzyl)triphenylphosphonium bromide With potassium tert-butylate In tetrahydrofuran at 0℃; Stage #2: 2,3-dimethyoxybenzaldehyde In tetrahydrofuran at 20℃; Wittig reaction; Further stages.; | 99% |
Conditions | Yield |
---|---|
Stage #1: 3-bromopropylamine hydrochloride With triethylamine In chloroform at 20℃; for 0.0833333h; Stage #2: 2,3-dimethyoxybenzaldehyde With magnesium sulfate In chloroform at 20℃; for 16h; | 99% |
N-(4-aminophenyl)-N'-phenylurea
2,3-dimethyoxybenzaldehyde
1-[4-(2,3-dimethoxy-benzylamino)phenyl]-3-phenylurea
Conditions | Yield |
---|---|
With sodium cyanoborohydride In methanol Reflux; Inert atmosphere; | 99% |
α,α-difluoromethyl p-tolyl sulfoxide
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
With potassium tert-butylate In tetrahydrofuran at -30℃; for 0.666667h; Inert atmosphere; diastereoselective reaction; | 99% |
Conditions | Yield |
---|---|
piperidine In pyridine Heating; | 98% |
With piperidine; pyridine at 120 - 130℃; Knoevenagel condensation; | 89% |
Stage #1: malonic acid; 2,3-dimethyoxybenzaldehyde With pyridine at 50℃; Inert atmosphere; Stage #2: With piperidine at 80 - 115℃; for 4h; Inert atmosphere; Stage #3: With hydrogenchloride In water | 84% |
Conditions | Yield |
---|---|
With hydrogenchloride; hydrogen; palladium on activated charcoal In methanol at 20℃; under 760.051 Torr; for 0.75h; | 98% |
With potassium hydroxide; hydrazine In diethylene glycol at 90 - 100℃; for 1.5h; | 81% |
With hydrogenchloride; amalgamated zinc; ethanol |
benzyloxy-trimethylsilane
(2R,3R)-(E)-Methyl 2-acetoxy-3-(dimethylphenylsilyl)-hex-4-enoate
2,3-dimethyoxybenzaldehyde
(E)-(2S,5S,6R)-Methyl 2-acetoxy-6-(benzyloxy)-6-(2,3-dimethoxyphenyl)-5-methylhex-3-enoate
Conditions | Yield |
---|---|
With trimethylsilyl trifluoromethanesulfonate In dichloromethane at -78℃; for 10h; | 98% |
trimethylsilyl trifluoromethanesulfonate In dichloromethane at -78℃; for 18h; | 97% |
Conditions | Yield |
---|---|
With lithium chloride In N,N-dimethyl-formamide for 22h; Heating; | 98% |
With aluminum (III) chloride In dichloromethane at -5 - 25℃; | 94% |
With cerium(III) chloride; sodium iodide In acetonitrile for 7h; dealkylation; Heating; | 89% |
With magnesium iodide for 10h; neat (no solvent); | 80% |
With n-butyllithium; lithium 4-methylpiperazin-1-ide In toluene 1.) 15 deg C, 20 min, 2.) 65-70 deg C; | 55% |
Conditions | Yield |
---|---|
With acetic acid at 60℃; for 0.333333h; Green chemistry; | 98% |
With nano-AlPO4(SO3H) In acetonitrile at 50℃; for 0.25h; | 89% |
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
Stage #1: diethyl 3-(allyloxy)-5-methoxybenzylphosphonate With sodium hydride In tetrahydrofuran; mineral oil at 0℃; for 0.5h; Horner-Wadsworth-Emmons Olefination; Stage #2: 2,3-dimethyoxybenzaldehyde In tetrahydrofuran at 0℃; Reflux; | 98% |
Conditions | Yield |
---|---|
With potassium hydroxide In methanol at 20℃; Claisen-Schmidt Condensation; | 98% |
3-fluoro-1-diethylphosphonomethyl-benzene
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
Stage #1: 3-fluoro-1-diethylphosphonomethyl-benzene With sodium hydride In tetrahydrofuran at 0 - 5℃; for 0.5h; Horner-Wadsworth-Emmons Olefination; Stage #2: 2,3-dimethyoxybenzaldehyde In tetrahydrofuran at 0 - 20℃; for 20h; Horner-Wadsworth-Emmons Olefination; | 98% |
2-Hydroxy-1,4-naphthoquinone
methyl 2-cyanoacetate
2,3-dimethyoxybenzaldehyde
Conditions | Yield |
---|---|
With ammonium acetate In ethanol; water at 20℃; for 0.116667h; Sonication; | 98% |
(1S,2S)-trans-2-amino-1-indanol
2,3-dimethyoxybenzaldehyde
(+)-(1S,2S)-2-(2,3-dimethoxybenzylideneamino)indan-1-ol
Conditions | Yield |
---|---|
In benzene for 10h; | 97.1% |
morpholine
Sesamol
2,3-dimethyoxybenzaldehyde
6-((2,3-dimethoxyphenyl)(morpholino)methyl)benzo[d][1,3]dioxol-5-ol
Conditions | Yield |
---|---|
In methanol Heating; | 97% |
In neat (no solvent) at 125℃; for 0.166667h; Solvent; Reagent/catalyst; Microwave irradiation; | 87% |
In ethanol Reflux; | 57% |
Methyltriphenylphosphonium bromide
2,3-dimethyoxybenzaldehyde
1-ethenyl-2,3-dimethoxybenzene
Conditions | Yield |
---|---|
Stage #1: Methyltriphenylphosphonium bromide With sodium amide In diethyl ether at 20℃; for 10h; Inert atmosphere; Stage #2: 2,3-dimethyoxybenzaldehyde In diethyl ether at -10 - 20℃; Wittig reaction; Inert atmosphere; | 97% |
Stage #1: Methyltriphenylphosphonium bromide With potassium tert-butylate In tetrahydrofuran at -30℃; for 1h; Wittig Olefination; Stage #2: 2,3-dimethyoxybenzaldehyde In tetrahydrofuran at -5 - 20℃; Wittig Olefination; | 91% |
With Amberlite IR-400 In N,N-dimethyl-formamide at 95℃; for 10h; Inert atmosphere; | 86% |
Stage #1: Methyltriphenylphosphonium bromide With potassium hexamethylsilazane In tetrahydrofuran at 20℃; for 3h; Wittig Olefination; Inert atmosphere; Stage #2: 2,3-dimethyoxybenzaldehyde In tetrahydrofuran for 18h; Wittig Olefination; Inert atmosphere; Reflux; | 72% |
Stage #1: Methyltriphenylphosphonium bromide In tetrahydrofuran at 0℃; for 0.5h; Inert atmosphere; Alkaline conditions; Stage #2: 2,3-dimethyoxybenzaldehyde In tetrahydrofuran at 0℃; for 12h; Inert atmosphere; |
2-amino-1-tert-butyl-4-cyanopyrrole
dimedone
2,3-dimethyoxybenzaldehyde
C26H31N3O3
Conditions | Yield |
---|---|
With L-proline In ethanol for 6h; Reflux; | 97% |
3-aminoethyl-2-[(p-trifluoromethoxy)anilino]quinazolin-4(3H)-one
2,3-dimethyoxybenzaldehyde
C26H23F3N4O4
Conditions | Yield |
---|---|
In ethanol at 75℃; for 3h; | 97% |
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