Product Name: White Mustard Seed Extract Latin Name: Semen Brassicae Plant source: The Seed of Brassica alba (L.) Boiss. Ratio extract: 10:1 20:1 Part Used: Seed Active Ingredient: Sinalbin by HPLC/UV Specs: 10%-20% Quality
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inquiryDensity: 1.1478 (rough estimate) Melting point:~202 ° C Boiling point: 285.61 ° C (rough estimate) Flash point: 158.6 ° C Water solubility: insoluble Steam pressure: 3.12E-07mmHg at 25 ° C Solubility: H2O: slightly soluble Refractive
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Min.Order:5 Kilogram
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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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inquiryAbout Product Details Items Specifications Test Results Appearance White to white crystalline powde
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inquiryOur company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At prese
Cas:530-59-6
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inquiry4-Hydroxy-3,5-dimethoxycinnamic acid CAS:530-59-6 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 qualit
Cas:530-59-6
Min.Order:1 Gram
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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
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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
Chengdu Biopurify Phytochemicals 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 Medic
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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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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inquiryZibo Hangyu Biotechnology Development 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 chemi
Cas:530-59-6
Min.Order:10 Gram
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inquiryProduct name: 4-Hydroxy-3,5-Dimethoxycinnamic Acid CAS No.:530-59-6 Molecule Formula:C11H12O5 Molecule Weight:224.21 Purity: 99.0% Package: 25kg/drum Description:White powder Manufacture Standards:Enterprise Standard TESTING ITEM
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Min.Order:1 Kilogram
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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,
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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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Min.Order:10 Milligram
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inquiryHangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
Stock products, own laboratoryAppearance:Off-white to light yellow powder Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
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inquiryAppearance:Solid powder Storage:Sealed,light and oxygen resistant Package:Foil bag or drum Application:Applied in dietary supplements,pharmaceutical or cosmeticeuticals Transportation:by sea or air Port:Beijing or Guangzhou Port
The quality is guaranteed. If you find the product is wrong compared with COA, we promise 100% refund or change product. COA and HPLC will be shipped out with goods. You can also inform your analysis method and we will follow your analysis me
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inquiryhigh purity,in stock Package:25kg/drum,or as per customers'demand Application:API,Pharmaceutical intermediates Transportation:air,sea,courier
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Min.Order:0
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inquiryJinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
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inquirytrans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
With potassium tert-butylate In isopropyl alcohol at 120℃; for 24h; | 94% |
malonic acid
syringic aldehyde
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
With aniline In pyridine at 60℃; Darkness; | 85% |
Stage #1: malonic acid; syringic aldehyde With piperazine; pyridine; p-toluidine In toluene at 80℃; for 3h; Stage #2: With potassium carbonate In water; toluene at 20℃; for 0.166667h; | 83.7% |
With piperidine; pyridine |
3-methyl-4-nitro-5-<2-(3,5-dimethoxy-4-hydroxyphenyl)ethenyl>isoxazole
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
With sodium hydroxide for 2h; Heating; | 72.9% |
ethyl-(4'-acetoxy-3',5'-dimethoxyphenyl)-prop-2-enoate
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
With potassium hydroxide In water Heating; |
alatanin 1
A
cyanidin 3-O-gentiobioside
B
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
With hydrogenchloride at 60℃; for 24h; |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
With sodium hydroxide Heating; |
A
gentibiose
B
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
With sodium hydroxide for 24h; Ambient temperature; |
A
trans-3,5-dimethoxy-4-hydroxycinnamic acid
B
5,7-dihydroxy-3-[β-D-glucopyranosyl-(1->2)-β-D-glucopyranosyl-(1->2)-β-D-glucopyranosyl]-2-(3,4-dihydroxyphenyl)-4H-1-benzopyran-4-one
Conditions | Yield |
---|---|
With sodium hydroxide In sodium hydroxide for 24h; Product distribution; Ambient temperature; other reagent; |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
With potassium hydroxide |
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water at 60℃; for 4h; |
4-acetoxy-3,5-dimethoxybenzaldehyde
sodium acetate
acetic anhydride
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
Stage #1: 4-acetoxy-3,5-dimethoxybenzaldehyde; sodium acetate; acetic anhydride at 145 - 150℃; for 12h; Perkin Reaction; Stage #2: With sodium hydroxide; water Stage #3: With hydrogenchloride In water pH=3; Product distribution / selectivity; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 37.6 percent / piperidine 2: 72.9 percent / 1 N aq. NaOH / 2 h / Heating View Scheme |
trans-p-sinapoyl β-D-glucopyranoside
B
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
1-O-sinapoyl-β-glucose:L-malate sinapoyltransferase In dimethyl sulfoxide at 30℃; pH=6.0; |
trans-p-sinapoyl β-D-glucopyranoside
B
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
1-O-sinapoyl-β-glucose:L-malate sinapoyltransferase In dimethyl sulfoxide at 30℃; pH=8.0; |
trans-p-sinapoyl β-D-glucopyranoside
A
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
1-O-sinapoyl-β-glucose:L-malate sinapoyltransferase In dimethyl sulfoxide at 30℃; pH=6.0; |
(8R,7'S,8'R)-5,5'-dimethoxylariciresinol 9'-O-β-D-(6-O-E-4-hydroxy-3,5-dimethoxycinnamoyl)glucopyranoside
A
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
With sodium hydroxide; water at 20℃; for 1h; Inert atmosphere; |
3-α-trans-sinapoyloxyjhanol 18-O-β-D-glucopyranoside
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
With methanol; potassium hydroxide for 5h; Reflux; |
A
1,3-dimethoxy-2-hydroxy-benzene
B
2,6-dimethoxy-p-quinone
C
3-methoxy-4-hydroxybenzoic acid
D
trans-3,5-dimethoxy-4-hydroxycinnamic acid
E
vanillin
F
syringic aldehyde
Conditions | Yield |
---|---|
With manganese(II) nitrate at 100℃; under 6000.6 Torr; Ionic liquid; Autoclave; |
diazomethane
4-O-[(E)-4-hydroxy-3,5-dimethoxycinnamoyl]bergenin
A
trans-3,5-dimethoxy-4-hydroxycinnamic acid
B
methyl 3,4,5-trimethoxycinnamate
Conditions | Yield |
---|---|
Stage #1: 4-O-[(E)-4-hydroxy-3,5-dimethoxycinnamoyl]bergenin With trifluoroacetic acid In water for 40h; Reflux; Stage #2: diazomethane In diethyl ether at 4℃; for 3h; |
A
D-Glucose
B
malonic acid
C
p-Coumaric Acid
D
trans-3,5-dimethoxy-4-hydroxycinnamic acid
E
peonidin chloride
Conditions | Yield |
---|---|
With hydrogenchloride; water at 100℃; for 1h; |
canolol
potassium hydrogencarbonate
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
With phenolic acid decarboxylase from Pantoea sp. In aq. phosphate buffer; acetonitrile at 30℃; for 24h; pH=8.5; Reagent/catalyst; Sealed tube; Enzymatic reaction; |
Conditions | Yield |
---|---|
With water; trifluoroacetic acid |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
Alkaline conditions; |
Conditions | Yield |
---|---|
With sulfuric acid for 24h; Reflux; | 100% |
With sulfuric acid Reflux; | 100% |
With sulfuric acid for 6h; Reflux; | 100% |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
trans-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxy-1,2-dihydronaphthalene-2,3-dicarboxylic acid
Conditions | Yield |
---|---|
With oxygen In water for 24h; var. pH; also with var. antioxidants; | 100% |
With air In water | |
With air; phosphate-boric acid buffer at 22℃; pH=7; Kinetics; Further Variations:; pH-values; Reagents; Oxidation; | |
Multi-step reaction with 3 steps 1: AcCl / 16 h 2: 52 percent / aq. FeCl3 / methanol / 48 h 3: 60 percent / aq. NaOH / 16 h / 20 °C View Scheme |
Conditions | Yield |
---|---|
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine In dichloromethane; N,N-dimethyl-formamide at 0 - 20℃; for 2.5h; Inert atmosphere; | 100% |
ethanol
trans-3,5-dimethoxy-4-hydroxycinnamic acid
ethyl (2E)-3-[4-hydroxy-3,5-bis(methyloxy)phenyl]-2-propenoate
Conditions | Yield |
---|---|
With acetyl chloride for 12h; | 98% |
With sulfuric acid at 100℃; for 5.5h; | 93.6% |
With hydrogenchloride In water Reflux; | 83% |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
dihydrosinapic acid
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In methanol at 25℃; under 2585.81 Torr; | 94% |
With sodium hydroxide anschliessend Behandeln mit einer Nickel-Aluminium-Legierung; | |
With ethanol; nickel at 110℃; under 110326 Torr; Hydrogenation; | |
With hydrogen; palladium on activated charcoal for 3h; | |
With hydrogen; 5%-palladium/activated carbon In ethanol at 120℃; under 76005.1 Torr; for 5h; |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
acetic anhydride
(E)-4-acetoxy-3,5-dimethoxycinnamic acid
Conditions | Yield |
---|---|
With pyridine at 20℃; for 3h; | 94% |
With pyridine at 20℃; | 70% |
With pyridine at 100℃; for 3h; |
ethyl 2-[N-methyl-N-(octyloxyacetyl)amino]-4-aminobenzoate
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran; water; N,N-dimethyl-formamide; toluene | 94% |
1-octadecanol
trans-3,5-dimethoxy-4-hydroxycinnamic acid
trans-octadecyl 3-(3,5-dimethoxy-4-hydroxyphenyl)propenoate
Conditions | Yield |
---|---|
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 20℃; Mitsunobu reaction; | 90% |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
tert-butyldimethylsilyl chloride
dimethyl (2S,2E)-2-((3-(4-hydroxy-3,5-dimethoxyphenyl)acryloyl)oxy)succinate
Conditions | Yield |
---|---|
Stage #1: trans-3,5-dimethoxy-4-hydroxycinnamic acid With 1H-imidazole In N,N-dimethyl-formamide Stage #2: tert-butyldimethylsilyl chloride In N,N-dimethyl-formamide at 0℃; for 1h; Stage #3: With potassium carbonate In tetrahydrofuran; methanol; water | 86% |
Stage #1: trans-3,5-dimethoxy-4-hydroxycinnamic acid; tert-butyldimethylsilyl chloride With 1H-imidazole In N,N-dimethyl-formamide at 0 - 20℃; for 4h; Stage #2: With potassium carbonate In methanol; water at 20℃; for 0.5h; | 72.9% |
p-hydroxyphenethyl alcohol
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Tyrosol synapate
Conditions | Yield |
---|---|
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃; for 48h; Mitsunobu Displacement; chemoselective reaction; | 85% |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
Stage #1: trans-3,5-dimethoxy-4-hydroxycinnamic acid; N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-isobutyl-4-(methylthio)benzenesulfonamide With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 0 - 25℃; for 1.16667h; Inert atmosphere; Stage #2: With dmap In N,N-dimethyl-formamide at 25℃; for 2h; Inert atmosphere; | 85% |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
Stage #1: trans-3,5-dimethoxy-4-hydroxycinnamic acid; N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-4-methoxy-N-propylbenzenesulfonamide With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 0 - 25℃; for 1.16667h; Inert atmosphere; Stage #2: With dmap In N,N-dimethyl-formamide at 25℃; for 2h; Inert atmosphere; | 84% |
Conditions | Yield |
---|---|
In methanol at 25 - 35℃; for 0.25h; | 83% |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-isobutyl-4-methoxybenzenesulfonamide
Conditions | Yield |
---|---|
Stage #1: trans-3,5-dimethoxy-4-hydroxycinnamic acid; N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-isobutyl-4-methoxybenzenesulfonamide With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 0 - 25℃; for 1.16667h; Inert atmosphere; Stage #2: With dmap In N,N-dimethyl-formamide at 25℃; for 2h; Inert atmosphere; | 83% |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
Stage #1: trans-3,5-dimethoxy-4-hydroxycinnamic acid; N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-isobutyl-6-methoxypyridine-3-sulfonamide With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 0 - 25℃; for 1.16667h; Inert atmosphere; Stage #2: With dmap In N,N-dimethyl-formamide at 25℃; for 2h; Inert atmosphere; | 82% |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
4-(2-aminoethyl)-1-(phenylmethyl)piperidine
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 0 - 20℃; for 12h; | 80% |
Conditions | Yield |
---|---|
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃; for 48h; Mitsunobu Displacement; chemoselective reaction; | 80% |
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 24h; | 79% |
tert-butylisonitrile
2-bromobenzylamine
2-benzoyloxyacetaldehyde
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
Stage #1: 2-bromobenzylamine; 2-benzoyloxyacetaldehyde With hydrogenchloride; triethylamine In methanol at 20℃; for 1h; Ugi Condensation; Inert atmosphere; Stage #2: tert-butylisonitrile; trans-3,5-dimethoxy-4-hydroxycinnamic acid In methanol at 20℃; for 48h; Ugi Condensation; Inert atmosphere; | 79% |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
Stage #1: trans-3,5-dimethoxy-4-hydroxycinnamic acid; N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-isopropyl-4-methoxybenzenesulfonamide With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 0 - 25℃; for 1.16667h; Inert atmosphere; Stage #2: With dmap In N,N-dimethyl-formamide at 25℃; for 2h; Inert atmosphere; | 79% |
tert-butylisonitrile
2-benzoyloxyacetaldehyde
trans-3,5-dimethoxy-4-hydroxycinnamic acid
(2-bromo-4,5-dimethoxyphenyl)methanamine
Conditions | Yield |
---|---|
Stage #1: 2-benzoyloxyacetaldehyde; (2-bromo-4,5-dimethoxyphenyl)methanamine With hydrogenchloride; triethylamine In methanol at 20℃; for 1h; Ugi Condensation; Inert atmosphere; Stage #2: tert-butylisonitrile; trans-3,5-dimethoxy-4-hydroxycinnamic acid In methanol at 20℃; for 48h; Ugi Condensation; Inert atmosphere; | 78% |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
Stage #1: trans-3,5-dimethoxy-4-hydroxycinnamic acid; N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-cyclopropyl-4-methoxybenzenesulfonamide With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 0 - 25℃; for 1.16667h; Inert atmosphere; Stage #2: With dmap In N,N-dimethyl-formamide at 25℃; for 2h; Inert atmosphere; | 78% |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
thiophenol
-3 thiopropene-2 oate de S-phenyle
Conditions | Yield |
---|---|
With fluoro-2 methyl-1 pyridinium; triethylamine In dichloromethane at -20℃; for 2h; | 77% |
Conditions | Yield |
---|---|
With sodium hydroxide; sodium chloride; potassium carbonate In N-methyl-acetamide; ethanol; water | 77% |
With sodium hydroxide; sodium chloride; potassium carbonate In N-methyl-acetamide; ethanol; water | 77% |
Cyclohexyl isocyanide
2-bromobenzylamine
2-benzoyloxyacetaldehyde
trans-3,5-dimethoxy-4-hydroxycinnamic acid
Conditions | Yield |
---|---|
Stage #1: 2-bromobenzylamine; 2-benzoyloxyacetaldehyde With hydrogenchloride; triethylamine In methanol at 20℃; for 1h; Ugi Condensation; Inert atmosphere; Stage #2: Cyclohexyl isocyanide; trans-3,5-dimethoxy-4-hydroxycinnamic acid In methanol at 20℃; for 48h; Ugi Condensation; Inert atmosphere; | 76% |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
3-(3,4-dimethylphenyl)propylamine
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In acetonitrile at 0 - 20℃; | 75% |
Conditions | Yield |
---|---|
With Ankistrodesmus braunii C202.7a Microbiological reaction; | A 5% B 75% |
trans-3,5-dimethoxy-4-hydroxycinnamic acid
2,6-bis(4'-hydroxy-3',5'-dimethoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane-4,8-dione
Conditions | Yield |
---|---|
With iron(III) chloride In ethanol at 20℃; for 1h; | 75% |
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