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Cas:99-14-9
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
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Min.Order:0 Metric Ton
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Cas:99-14-9
Min.Order:1 Gram
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Type:Manufacturers
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Min.Order:5 Kiloliter
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Min.Order:1 Kilogram
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Min.Order:1 Kilogram
FOB Price: $139.0 / 210.0
Type:Trading Company
inquiryAppearance:White crystalline powder Storage:ln stock Package:25kg/Barrel Application:Chemicals Transportation:Express/Sea/Air Port:Any port of china
Cas:99-14-9
Min.Order:1 Kilogram
FOB Price: $100.0 / 169.0
Type:Lab/Research institutions
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Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryTRICARBALLYLIC ACID CAS:99-14-9 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 organic interme
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Min.Order:1 Gram
Negotiable
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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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Min.Order:1 Kilogram
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Appearance:white powder Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Peptide bond condensing agent Transportation:Common products:Sea/Air/Courier Dangerous Che
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Min.Order:100 Metric Ton
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Cas:99-14-9
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiryProduct name: Tricarballylic Acid CAS No.:99-14-9 Molecule Formula:C6H8O6 Molecule Weight:176.12 Purity: 99.0% Package: 25kg/drum Description:White powder Manufacture Standards:Enterprise Standard TESTING ITEMS SP
Cas:99-14-9
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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Min.Order:1 Kilogram
FOB Price: $50.0 / 100.0
Type:Trading Company
inquiryProduct Name: TRICARBALLYLIC ACID CAS: 99-14-9 MF: C6H8O6 MW: 176.12 EINECS: 202-733-3 Product Categories: Mol File: 99-14-9.mol TRICARBALLYLIC ACID Structure TRICARBALLYLIC ACID Chemical Properties Melting point 156-161 &d
factory?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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Min.Order:1 Kilogram
FOB Price: $18.0 / 20.0
Type:Trading Company
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
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stock,low price,high quality,high purity,good sevice Appearance:99-14-9 Storage:Preserve In Well-Closed, Light-Resistant and Tight Containers. Store In Cool & Dry Place Package:1g,5g,50g,100g,1kg...more Application:R&D Transportation:by land,by ai
1.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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Cas:99-14-9
Min.Order:0
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Type:Lab/Research institutions
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Lower 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
Cas:99-14-9
Min.Order:0
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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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Min.Order:1 bottle
Negotiable
Type:Lab/Research institutions
inquiryhigh quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Conditions | Yield |
---|---|
With HeMaRaphos; water; toluene-4-sulfonic acid; palladium dichloride In tetrahydrofuran at 125℃; under 30003 Torr; for 24h; Autoclave; Green chemistry; regioselective reaction; | 86% |
Dimethyl 2-dimethoxycarbonylmethyl-3-nitro-1,1-cyclopropanedicarboxylate
tricarallylic acid
Conditions | Yield |
---|---|
With hydrogenchloride for 10h; Heating; | 70% |
With hydrogenchloride for 10h; Product distribution; Mechanism; Heating; | 70% |
(-)-3-dehydroshikimic acid
A
3,4-Dihydroxybenzoic acid
B
tricarallylic acid
C
3,4,5-trihydroxybenzoic acid
D
dihydrogallic acid
E
2-hydroxyresorcinol
Conditions | Yield |
---|---|
With air; Na1.5H1.5PO4 at 40℃; for 50h; Rate constant; Mechanism; other oxidant, var. time; | A 12 % Spectr. B 14 % Spectr. C 13% D n/a E 3 % Spectr. |
methanol
citraconic acid dimethyl ester
potassium cyanide
A
dimethyl 2-(methoxymethyl)succinate
B
tricarallylic acid
Conditions | Yield |
---|---|
at 25℃; und Behandeln des Reaktionsprodukts mit HCl oder NaOH bei 25grad; |
methanol
citraconic acid dimethyl ester
potassium cyanide
tricarallylic acid
Conditions | Yield |
---|---|
at 25℃; beim Kochen des Reaktionsprodukts mit HCl oder NaOH; |
2,3-Dichloroprop-1-ene
ethanol
potassium cyanide
tricarallylic acid
Conditions | Yield |
---|---|
zerlegt das Prokukt mit alkoholischem Kali; |
Conditions | Yield |
---|---|
With ethanol Zerlegen des Reaktionsproduktes mit alkohol.Kalilauge; |
Conditions | Yield |
---|---|
With nitric acid |
Conditions | Yield |
---|---|
With ethanol Zerlegen des Reaktionsproduktes mit Kaliumhydroxyd; |
Conditions | Yield |
---|---|
With bacterium succinicum n.sp; phosphate-buffer |
Conditions | Yield |
---|---|
durch Natriumamalgam; | |
Durch elektolitische Reduktion von halb mit Natron neutralisierter Aconitsaeure in der Kaelte unter Verwendung einer Quecksilberkathode; | |
With sodium amalgam bei der Reduktion der Aconitsaeure mit Natriumamalgam entstehende Loesung des Natriumsalzes nach starker Verduennung mit Bleizucker und zerlegt den Niederschlag durch Schwefelwasserstoff; |
Conditions | Yield |
---|---|
With water; platinum Hydrogenation; |
Conditions | Yield |
---|---|
Hydrogenation; | |
With water; platinum Hydrogenation; |
Conditions | Yield |
---|---|
bei nachfolgenden Verseifung; |
propane-1,2,2,3-tetracarboxylic acid
A
tricarallylic acid
B
methylammonium carbonate
Conditions | Yield |
---|---|
at 151℃; |
Conditions | Yield |
---|---|
With potassium hydroxide; ethanol |
Conditions | Yield |
---|---|
With hydrogenchloride; potassium chlorate at 90℃; extrahiert mit Aether,trennt aus dem Aetherabdampfungsrueckstand die auskrystallisierende Trichlorbrenztraubensaeure ab und kocht die verduennte Mutterlauge mit Zinn und Salzsaeure; |
Conditions | Yield |
---|---|
beim Ozonisieren und folgenden Behandeln mit Kaliumpermanganat-Loesung bei 0grad.; |
3,4-dioxo-cyclopentanecarboxylic acid
tricarallylic acid
Conditions | Yield |
---|---|
With potassium hydroxide; dihydrogen peroxide |
4-carboxy-2,6-dihydroxypyridine
tricarallylic acid
Conditions | Yield |
---|---|
With hydrogenchloride; tin |
sodium diethylmalonate
diethyl Fumarate
tricarallylic acid
Conditions | Yield |
---|---|
dann Kochen den erhaltenen Propan-α.α.β.γ-tetracarbonsaeure-tetraaethylester mit maessig verduennter Salzsaeure; | |
dann Kochen den erhaltenen Propan-α.α.β.γ-tetracarbonsaeure-tetraaethylester mit konz.Kalilauge; |
potassium cyanide
E-Ethyl β-chlorocrotonate
A
2-methylenesuccinic acid
B
tricarallylic acid
Conditions | Yield |
---|---|
und nachfolgender Verseifung mit Kali; |
Conditions | Yield |
---|---|
With ethanol Zerlegen des Reaktionsproduktes mit Kaliumhydroxyd; |
2-<2,2,2-Trinitro-ethyl>-bernsteinsaeure
tricarallylic acid
Conditions | Yield |
---|---|
(hydrolysis); |
tricarallylic acid
Conditions | Yield |
---|---|
With hydrogenchloride at 110 - 120℃; Heating; |
Conditions | Yield |
---|---|
With sodium hydroxide; potassium permanganate |
(3-cyano-5-imino-2-oxo-pyrrolidin-3-yl)-acetonitrile
sulfuric acid
tricarallylic acid
Conditions | Yield |
---|---|
at 80℃; for 72h; High pressure; Sealed tube; | 91% |
Conditions | Yield |
---|---|
Stage #1: tricarallylic acid With caesium carbonate In N,N-dimethyl-formamide for 0.5h; Schlenk technique; Inert atmosphere; Stage #2: (bromomethyl)pentafluorobenzene In N,N-dimethyl-formamide at 20℃; for 16h; Schlenk technique; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
With acetic anhydride 1.) 45 deg C, 1h 2.) glacial CH3COOH, 65 deg C, 1h; | 87% |
With acetic anhydride at 20℃; | 77.8% |
beim Destillieren unter vermindertem Druck; |
tricarallylic acid
2-fluorobenzoic anhydride
Conditions | Yield |
---|---|
With pyridine In m-xylene at 140℃; | 85% |
tricarallylic acid
Conditions | Yield |
---|---|
With pyridine; triphenyl phosphite In 1-methyl-pyrrolidin-2-one at 100℃; for 4h; | 80% |
Conditions | Yield |
---|---|
In H2O Eu-compd. and carboxy-compd. in H2O refluxed for 8 h; concentrated, EtOH added, washed with EtOH, dried in vac. at 80°Cfor 2 h, elem. anal.; | 80% |
tricarallylic acid
benzoic acid anhydride
6a-phenyldihydrofuro[2,3-b]furan-2,5(3H,6aH)-dione
Conditions | Yield |
---|---|
With pyridine In m-xylene at 140℃; | 78% |
at 150 - 160℃; |
Conditions | Yield |
---|---|
In water at 80℃; for 72h; High pressure; Sealed tube; | 78% |
Conditions | Yield |
---|---|
In H2O Ni-compd. and carboxy-compd. in H2O refluxed for 8 h; concentrated, EtOH added, washed with EtOH, dried in vac. at 80°Cfor 2 h, elem. anal.; | 75% |
Conditions | Yield |
---|---|
With 4-methyl-morpholine; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide In dichloromethane at 20℃; | 75% |
With 4-methyl-morpholine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; | 75% |
1,3-diazido 2-propanol
tricarallylic acid
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; Green chemistry; | 73% |
Conditions | Yield |
---|---|
Stage #1: tricarallylic acid With thionyl chloride In N,N-dimethyl-formamide at 90℃; for 2h; Stage #2: dibutylamine With triethylamine In dichloromethane; N,N-dimethyl-formamide for 120h; | 72% |
Stage #1: tricarallylic acid With thionyl chloride; N,N-dimethyl-formamide at 90℃; for 2h; Stage #2: dibutylamine With triethylamine In dichloromethane for 120h; | 72% |
tricarallylic acid
2-chlorobenzoic anhydride
Conditions | Yield |
---|---|
With pyridine In m-xylene at 140℃; | 70% |
Conditions | Yield |
---|---|
With sulfuric acid In toluene at 190℃; for 24h; | 68% |
Conditions | Yield |
---|---|
In ethanol; water wet Zn(OH)2 was suspn. in water, 0.5 M soln. of tricarballylic acid was added, a soln. of pyridine-compound in abs. ethanol was added dropwise, left overnight; elem. anal.; | 68% |
tricarallylic acid
3-fluorobenzoic acid anhydride
Conditions | Yield |
---|---|
With pyridine In m-xylene at 140℃; | 68% |
Conditions | Yield |
---|---|
tricresole borate In xylene for 3h; Product distribution / selectivity; Heating / reflux; | 67.2% |
Conditions | Yield |
---|---|
In ethanol; water wet Zn(OH)2 was suspn. in water, 0.5 M soln. of tricarballylic acid was added, a soln. of bipyridine in abs. ethanol was added dropwise, left overnight; elem. anal.; | 67% |
Conditions | Yield |
---|---|
In H2O Cr-compd. dissolved in H2O, 1 M NaOH added, centrifuged, washed with H2O, dispersed in H2O with carboxy-compd. under continuosly stirring, refluxed for 8 h; cooled, filtered, concentrated, EtOH added, dried at 80°C for 2 h, dried in vac., elem. anal.; | 65% |
Conditions | Yield |
---|---|
tricresole borate In xylene for 3h; Product distribution / selectivity; Heating / reflux; | 63% |
Stage #1: tricarallylic acid With pyridine; diisopropyl-carbodiimide at 50℃; for 3h; Stage #2: 2-METHYLCYCLOHEXYLAMINE for 8h; | 61% |
Stage #1: tricarallylic acid With pyridine; diisopropyl-carbodiimide at 50℃; for 3h; Stage #2: 2-METHYLCYCLOHEXYLAMINE for 8h; | 61% |
Conditions | Yield |
---|---|
In ethanol; water wet Zn(OH)2 was suspn. in water, 0.5 M soln. of tricarballylic acid was added, a soln. of phenanthroline in abs. ethanol was added dropwise, left overnight; elem. anal.; | 61% |
Conditions | Yield |
---|---|
With pyridine In m-xylene at 140℃; | 61% |
tricarallylic acid
Conditions | Yield |
---|---|
In water byproducts: H(1+); reaction of Gd(tricarballylateH)(1+) with tricarballylic acid at pH 3.00; nuclear magnetic relaxation; | 60% |
Conditions | Yield |
---|---|
With NaOH In water High Pressure; by a react. of Mn-contg. compd. (0.5 mmol), tricarballylic acid (0.25 mmol), NaOH (1 mmol) in aq. soln. in Teflon-lined autoclave; heating at 160°C for 120 h; cooling over a period of 12 h at a rate of 10°C/h; crystals were collected by filtration, washed with water, and dried at ambient temp.; elem. anal.; | 59% |
tricarallylic acid
4-(trifluoromethyl)benzoic anhydride
Conditions | Yield |
---|---|
With pyridine In m-xylene at 140℃; | 59% |
Conditions | Yield |
---|---|
With calcium chloride at 150℃; for 8h; | 57% |
tricarallylic acid
Chloroacetic anhydride
1-chloromethyl-2,8-dioxabicyclo[3.3.0]octane-3,7-dione
Conditions | Yield |
---|---|
With dmap at 180℃; under 200 Torr; for 3h; | 56% |
tricarallylic acid
3-methylbenzoic acid anhydride
Conditions | Yield |
---|---|
With pyridine In m-xylene at 140℃; | 56% |
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