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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inquiryUnique advantages Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:White to off-white powder Storage:cool dry place Package:25kg/drum Application:cosmetic raw meterial Transportati
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inquiry1. Factory price and high quality must be guaranteed, base on 8 years of production and R&D experience2. Free samples will be provided,ensure specifications and quality are right for customer3. Customers will receive the most professional technical s
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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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inquiryPRODUCT DETAILS
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inquiryOur advantages: 1, High quality with competitive price: 1) Standard:BP/USP/EP/Enterprise standard 2) All Purity≥99% 3) We are manufacturer and can provide high quality products with factory price. 2, Fast and safe delivery 1) Parcel can be
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inquiry1.In No Less 10 years exporting experience. you 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 Specializ
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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
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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
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inquiryA substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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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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inquiryProduct name: 4-Hydroxy-3-Methoxycinnamic Acid Methyl Ester CAS No.: 2309-07-1 Molecule Formula:C11H12O4 Molecule Weight:208.21 Purity: 99.0% Package: 25kg/drum Description:White crystalline powder Manufacture Standards:Enterprise Standard
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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,
FERULIC ACID METHYL ESTER Basic information Product Name: FERULIC ACID METHYL ESTER Synonyms: FERULIC ACID METHYL ESTER (METHYL FERULATE);(SYNONYMS: METHYL FERULATE);Methyl Ferulate [4-Hydroxy-3-MethoxycinnaMic Acid Methyl Ester];METHYL 4-HYDR
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inquiryHubei CuiRan Biotechnology Co., Ltd is a leading company in the research, development, manufacture and marketing of High Quality Phytochemicals and Extracts(especially Active Ingredients from Traditional Chinese Medicine,Traditional Chinese Medicine)
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inquiryZhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
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inquiryProduct name: 4-Hydroxy-3-Methoxycinnamic Acid Methyl Ester Chemical name: Ferulic Acid Methylester CAS No: 2309-07-1 Molecular formula: C11H12O4 Molecular weight: 208.21 Appearance: White crysraline power Appearance:White crysraline power Stor
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inquiryLower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
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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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inquiryQ1: Are you a manufacturer Answer: Yes, we are factory founded on 2012.Q2: How to contact with us Click "contact supplier" And then send us message the product you interest in, you will get reply within 12 hours.Q3:Which kind of payment terms do you
Acmec 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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inquiryOur clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
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inquiryMethyl 4-hydroxy-3-methoxycinnamateAppearance:detailed see specifications Storage:Keep away of light, cool place Package:25kg/drum;200kg/drum Application:It is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agr
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inquiryBOC Sciences provides a wide range of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell. https://www.bocsci.com/methyl-4-hydr
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Type:Trading Company
inquiryConditions | Yield |
---|---|
With Dowex 50 W x 8200-400 Heating; | 100% |
With thionyl chloride Ambient temperature; | 100% |
With sulfuric acid at 0℃; for 12h; Darkness; Reflux; | 99% |
methyl (E)-4-methoxymethyl-3-methoxycinnamate
Methyl ferulate
Conditions | Yield |
---|---|
With hydrogenchloride In methanol for 0.5h; Heating; | 100% |
Conditions | Yield |
---|---|
In water at 90℃; for 0.5h; Horner-Wadsworth-Emmons Olefination; Green chemistry; | 99% |
In toluene at 150℃; for 0.166667h; Wittig Olefination; Inert atmosphere; Microwave irradiation; Sealed tube; stereoselective reaction; | 98% |
In toluene at 150℃; for 0.166667h; Sealed tube; Microwave irradiation; | 98% |
methanol
[(E)-3-(4-Hydroxy-3-methoxy-phenyl)-acryloyloxymethylene]-dimethyl-ammonium; chloride
Methyl ferulate
Conditions | Yield |
---|---|
98% |
Conditions | Yield |
---|---|
With sulfuric acid for 4h; Reflux; | 96% |
With sulfuric acid Fischer-Speier Esterification; Sealed tube; Heating; Microwave irradiation; |
acrylic acid methyl ester
Methyl ferulate
Conditions | Yield |
---|---|
With palladium diacetate In methanol at 20℃; Heck Reaction; | 96% |
Methyl ferulate
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran at 20℃; for 1h; Inert atmosphere; Schlenk technique; Glovebox; | 94% |
methyl (E)-3-(3-methoxy-4-((3-methylbut-2-en-1-yl)oxy)phenyl)acrylate
Methyl ferulate
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In dichloromethane at 20℃; for 2h; | 90% |
Conditions | Yield |
---|---|
With Hoveyda-Grubbs catalyst first generation In 1,2-dichloro-ethane at 70℃; Cross Metathesis; Schlenk technique; Inert atmosphere; Glovebox; | 90% |
Conditions | Yield |
---|---|
With sulfuric acid In methanol at 20℃; for 4h; | 84% |
Multi-step reaction with 2 steps 2: 98 percent View Scheme | |
With sulfuric acid In methanol; ice-water; diethyl ether; dichloromethane | |
Multi-step reaction with 3 steps 1.1: potassium carbonate / acetonitrile / 18 h / 70 °C / Inert atmosphere 1.2: 24 h / 660 °C / Inert atmosphere 2.1: methanol / 18 h / 20 °C / Inert atmosphere 3.1: bis-triphenylphosphine-palladium(II) chloride; ammonium formate / acetonitrile / 24 h / 80 °C / Inert atmosphere View Scheme |
(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid
dimethyl sulfate
Methyl ferulate
Conditions | Yield |
---|---|
With potassium hydrogencarbonate In acetone at 20℃; for 1.5h; | 84% |
Methyl ferulate
Conditions | Yield |
---|---|
With bis-triphenylphosphine-palladium(II) chloride; ammonium formate In acetonitrile at 80℃; for 24h; Inert atmosphere; | 71% |
methanol
A
3,5-di-O-β-D-glucopyranoside of cyanidin
B
cyanidin-3-glucoside
C
Methyl ferulate
Conditions | Yield |
---|---|
With hydrogenchloride at 65℃; for 4h; | A n/a B n/a C 70% |
diazomethane
(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid
Methyl ferulate
Conditions | Yield |
---|---|
In diethyl ether at 0℃; for 2h; | 69% |
With methanol | |
In diethyl ether Esterification; | |
In methanol at 20℃; for 4h; Methylation; |
(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid
choline chloride
Methyl ferulate
Conditions | Yield |
---|---|
With urea at 140℃; for 2h; Green chemistry; | 55% |
Conditions | Yield |
---|---|
With pyridine |
methanol
regaloside G
A
Methyl ferulate
B
2-O-β-D-glucosyl-glycerol
Conditions | Yield |
---|---|
With sodium methylate for 1h; Ambient temperature; |
methanol
cistanoside D
A
homovanillyl alcohol
B
Methyl ferulate
Conditions | Yield |
---|---|
With acetyl chloride for 0.5h; Heating; |
methanol
(E)-3-(4-Hydroxy-3-methoxy-phenyl)-acrylic acid 2-hydroxy-3-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-propyl ester
A
1-O-β-D-glucopyranosyl-sn-glycerol
B
Methyl ferulate
C
3-O-β-D-glucopyranosyl-sn-glycerol
Conditions | Yield |
---|---|
With sodium methylate |
sodium methylate
6'-O-trans-feruloylnodakenin
A
Methyl ferulate
B
1'-O-β-D-glucopyranosyl-(2R)-marmesin
Conditions | Yield |
---|---|
In methanol for 8h; Ambient temperature; |
sodium methylate
(+)-catechin 5-O-β-D-(2''-O-feruloyl-6''-O-p-coumaroyl)-glucopyranoside
A
methyl 4-hydroxycinnamate
B
Methyl ferulate
Conditions | Yield |
---|---|
In methanol for 0.166667h; Product distribution; Heating; |
regaloside G
A
Methyl ferulate
B
2-O-β-D-glucosyl-glycerol
Conditions | Yield |
---|---|
With sodium methylate In methanol for 1h; Ambient temperature; |
Conditions | Yield |
---|---|
With potassium methanolate In methanol for 48h; |
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water at 0℃; |
Rhynchophine
A
Methyl ferulate
B
3β(R)-vincosamide
Conditions | Yield |
---|---|
With sodium methylate In methanol | A 4 mg B 3 mg |
4-O-β-D-glucopyranosyl-(E)-ferulic acid methyl ester
Methyl ferulate
Conditions | Yield |
---|---|
With sulfuric acid In ethanol for 2h; |
(E)-3-(4-Hydroxy-3-methoxy-phenyl)-acrylic acid 2-hydroxy-3-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-propyl ester
A
1-O-β-D-glucopyranosyl-sn-glycerol
B
Methyl ferulate
C
3-O-β-D-glucopyranosyl-sn-glycerol
Conditions | Yield |
---|---|
With sodium methylate In methanol |
Conditions | Yield |
---|---|
With sodium methylate In methanol at 22℃; for 1h; |
methanol
(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid
A
Methyl ferulate
B
methyl (Z)-3-(4-hydroxy-3-methoxyphenyl)acrylate
Methyl <5-hydroxy-t-3-(4-hydroxy-3-methoxyphenyl)-6-methoxy-c-2-(methoxycarbonyl)-r-1-indanyl>acetate
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid for 6h; Heating; Further byproducts given; | A 1.5 g B 100 mg C 7.09 g D 280 mg |
Methyl ferulate
acetic anhydride
(E)-methyl 3-(4-acetoxy-3-methoxyphenyl)acrylate
Conditions | Yield |
---|---|
With pyridine | 100% |
With pyridine In ethyl acetate at 20℃; | 91% |
With triethylamine In dichloromethane at 20℃; for 4h; | 85% |
Methyl ferulate
methyl 3-(4-hydroxy-3-methoxyphenyl)propanoate
Conditions | Yield |
---|---|
With 5%-palladium/activated carbon; hydrogen In methanol | 100% |
With palladium 10% on activated carbon; hydrogen In methanol at 20℃; for 12h; | 98% |
With hydrogen; palladium 10% on activated carbon In methanol at 10 - 35℃; for 4h; | 97% |
Methyl ferulate
tert-butyldimethylsilyl chloride
methyl (2E)-3-[4-[[tert-butyldimethylsilyl]oxy]-3-methoxyphenyl]-prop-2-enoate
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 2h; | 99% |
Methyl ferulate
coniferal alcohol
Conditions | Yield |
---|---|
With diisobutylaluminium hydride In toluene | 98% |
With diisobutylaluminium hydride In dichloromethane at -78 - 20℃; for 1h; Inert atmosphere; stereoselective reaction; | 92% |
With lithium aluminium tetrahydride In diethyl ether at 20℃; for 12h; | 87% |
Methyl ferulate
benzyl bromide
(E)-3-(3-methoxy-4-(benzyloxy)phenyl)methyl acrylate
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 2h; | 98% |
With 18-crown-6 ether; potassium carbonate In toluene Heating; | 92% |
With potassium carbonate In acetone for 10h; Reflux; Inert atmosphere; | 92.5% |
Methyl ferulate
benzyl chloride
(E)-3-(3-methoxy-4-(benzyloxy)phenyl)methyl acrylate
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 70℃; for 6h; | 96.1% |
With potassium carbonate In N,N-dimethyl-formamide at 160℃; for 3h; Alkylation; |
Methyl ferulate
bromoacetic acid methyl ester
methyl 3-[2-methoxy-4-(methoxycarbonylmethoxy)phenyl]acrylate
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide Alkylation; | 94% |
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 0℃; for 24h; Inert atmosphere; | 91% |
Conditions | Yield |
---|---|
Stage #1: Methyl ferulate With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.25h; Stage #2: propargyl bromide In N,N-dimethyl-formamide at 0 - 20℃; for 23h; Inert atmosphere; | 91% |
Methyl ferulate
methyl (E)-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-5-(3-methoxy-3-oxoprop-1-enyl)-2,3-dihydrobenzofuran-3-carboxylate
Conditions | Yield |
---|---|
With dihydrogen peroxide; calcium chloride In methanol at 20℃; for 0.5h; pH=4; aq. buffer; Enzymatic reaction; regiospecific reaction; | 90% |
Conditions | Yield |
---|---|
With lithium hydroxide monohydrate In tetrahydrofuran; methanol; water at 20℃; for 18h; Inert atmosphere; Schlenk technique; Glovebox; | 89% |
With Sporotrichum thermophile type C feruloyl esterase; water Enzyme kinetics; |
Conditions | Yield |
---|---|
Stage #1: Methyl ferulate With sodium hydride In tetrahydrofuran; mineral oil at 0℃; for 0.166667h; Inert atmosphere; Stage #2: ethyl chloromethyl ether In tetrahydrofuran; mineral oil at 0 - 20℃; for 2h; Inert atmosphere; | 89% |
1-methyl-3-pyrrolidinol
Methyl ferulate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; triphenylphosphine In tetrahydrofuran at 0℃; for 0.5h; | 89% |
Methyl ferulate
Conditions | Yield |
---|---|
With [bis(acetoxy)iodo]benzene In methanol; dichloromethane at 25℃; for 14h; Diels-Alder reaction; Inert atmosphere; | 87% |
Conditions | Yield |
---|---|
With [bis(acetoxy)iodo]benzene In dichloromethane at 25℃; for 14h; | 87% |
Methyl ferulate
(2E)-3-(3-methoxy-4-hydroxyphenyl)-N-hydroxy-2-propenamide
Conditions | Yield |
---|---|
With hydroxylamine hydrochloride; sodium hydroxide In 1,4-dioxane; water at 20℃; for 24h; | 87% |
Methyl ferulate
N-(2-chloroacetyl)-3-chloro-4-fluoroaniline
Conditions | Yield |
---|---|
Stage #1: Methyl ferulate With potassium carbonate In acetone at 20℃; for 0.5h; Inert atmosphere; Stage #2: N-(2-chloroacetyl)-3-chloro-4-fluoroaniline In acetone for 10h; Reflux; Inert atmosphere; | 85.65% |
(+/-)-2-[1-(2-chloroacetoxy)pentyl]benzoic acid
Methyl ferulate
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 6h; | 85% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 24h; | 84% |
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