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Cas:147-73-9
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Cas:147-73-9
Min.Order:1 Gram
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Type:Lab/Research institutions
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Cas:147-73-9
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Type:Lab/Research institutions
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Cas:147-73-9
Min.Order:0 Metric Ton
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Type:Lab/Research institutions
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Cas:147-73-9
Min.Order:10 Gram
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Type:Lab/Research institutions
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Cas:147-73-9
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
inquiryfactory?direct?sale Application:healing drugs
Cas:147-73-9
Min.Order:0
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Type:Lab/Research institutions
inquiryfactory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Best quality & Attractive price & Professional service; Trial & Pilot & CommercialHenan Fine Chemicals Co., LTD. is a diversified technology - oriented integrated company, which mainly concentrates on fine chemicals. Our company is committed to becom
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FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the MESOTARTARIC ACID, CAS:147-73-9 with the most competitive price and the best quality.
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Cas:147-73-9
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inquiryConditions | Yield |
---|---|
With vanadia at 370℃; |
Conditions | Yield |
---|---|
With sodium chlorate; osmium(VIII) oxide; water at 50℃; | |
With hydrogenchloride; sodium chlorate; osmium(VIII) oxide at 50℃; |
Conditions | Yield |
---|---|
With osmium(VIII) oxide; barium chlorate; water | |
With osmium(VIII) oxide; silver(I) chlorate; water |
Conditions | Yield |
---|---|
With sodium chlorate; osmium(VIII) oxide; water at 50℃; | |
With hydrogenchloride; sodium chlorate; osmium(VIII) oxide at 50℃; |
Conditions | Yield |
---|---|
With nitric acid |
hexa-1,5-diene-3,4-diol
meso-tartaric acid
Conditions | Yield |
---|---|
With ozone; acetic acid Kochen des Diozonids und Erwaermen der mit Wasser verd.Loesung mit Brom auf 50grad,entsteht in analoger Reaktion aus Hydrocinnamoindiacetat; |
3-hydroxy-2-oxopropionic acid
potassium cyanide
A
D-tartaric acid
B
meso-tartaric acid
Conditions | Yield |
---|---|
beim Kochen des Reaktionsprodukts mit verd.Schwefelsaeure; |
DL-erythro-pentyne-(1)-triol-(3.4.5)
meso-tartaric acid
Conditions | Yield |
---|---|
With nitric acid at 50 - 55℃; |
D-digitxose
A
L-erythro-2.3-dihydroxy-glutaric acid
B
meso-tartaric acid
Conditions | Yield |
---|---|
With nitric acid at 90℃; |
Conditions | Yield |
---|---|
With nitric acid |
Conditions | Yield |
---|---|
With sodium vanadate; nitric acid | |
With sodium vanadate; nitric acid | |
With sodium vanadate; nitric acid |
(2S,3R)-3-aminoaspartic acid
meso-tartaric acid
Conditions | Yield |
---|---|
With nitric acid |
Conditions | Yield |
---|---|
With sodium hydroxide | |
With potassium hydroxide | |
With water at 165℃; |
Conditions | Yield |
---|---|
With water | |
With hydrogenchloride | |
With hydrogenchloride im geschlossenen Rohr; | |
With sodium hydroxide; water |
Conditions | Yield |
---|---|
With water at 165℃; | |
With hydrogenchloride | |
With alkaline solution ueber den Verlauf dieser Reaktion; |
(-)(2S:3S)-3-chloro-2-hydroxy-succinic acid
A
meso-tartaric acid
B
L-Tartaric acid
Conditions | Yield |
---|---|
With water |
Conditions | Yield |
---|---|
With zinc |
Conditions | Yield |
---|---|
With potassium hydroxide; water Darstellung; ueber mehrere Stufen; |
Conditions | Yield |
---|---|
With hydrogenchloride | |
With water | |
With alkaline solution |
Conditions | Yield |
---|---|
With osmium(VIII) oxide; potassium chlorate; water at 50℃; | |
With potassium permanganate | |
With sodium chlorate; osmium(VIII) oxide; water at 50℃; |
Conditions | Yield |
---|---|
With osmium(VIII) oxide; dihydrogen peroxide; tert-butyl alcohol |
Conditions | Yield |
---|---|
With nitric acid |
(2R,3R)-oxirane-2,3-dicarboxylic acid
A
meso-tartaric acid
B
L-Tartaric acid
Conditions | Yield |
---|---|
With water | |
With potassium hydroxide |
Conditions | Yield |
---|---|
With permanganate(VII) ion at 0℃; |
octyl alpha-D-glucopyranoside
A
tartronic acid
B
meso-tartaric acid
C
L-Tartaric acid
D
gluconic acid
E
D-glucaric acid
F
oxalic acid
Conditions | Yield |
---|---|
With oxygen; platinum on activated charcoal In water at 49.9℃; under 300.02 Torr; Product distribution; Mechanism; initial rate of consumption, pH effect; |
methyl-alpha-D-glucopyranoside
A
tartronic acid
B
D-glyceric acid
C
meso-tartaric acid
D
L-Tartaric acid
E
oxalic acid
Conditions | Yield |
---|---|
With oxygen; platinum on activated charcoal In water at 49.9℃; under 300.02 Torr; Product distribution; Mechanism; initial rate of consumption, pH effect; |
A
meso-tartaric acid
B
D-arabinuronic acid
C
(2S,4S)-xylaric acid
D
D-glucaric acid
Conditions | Yield |
---|---|
With phosphate buffer; dihydrogen peroxide; iron(II) sulfate In water at 37℃; for 6h; pH=7.4; Product distribution; Further Variations:; Reagents; Oxidation; |
water
dihydrogen peroxide
tert-butyl alcohol
benzene
A
meso-tartaric acid
B
oxalic acid
C
phenol
meso-tartaric acid
Conditions | Yield |
---|---|
With calcium hydroxide |
meso-tartaric acid
acetic anhydride
(3R,4S)-2,5-dioxotetrahydrofuran-3,4-diyl diacetate
Conditions | Yield |
---|---|
at 80℃; for 4h; | 98.73% |
With hydrogenchloride Acetylation; dehydration; | 51% |
With sulfuric acid at 120℃; for 1h; Inert atmosphere; | 37% |
With sulfuric acid for 4h; |
meso-tartaric acid
Conditions | Yield |
---|---|
In water at 20℃; for 2h; Darkness; | 97% |
meso-tartaric acid
Conditions | Yield |
---|---|
In isopropyl alcohol at 30℃; for 22h; | 95.63% |
meso-tartaric acid
5,5-difluoro-10-mesityl-1,3,7,9-tetramethyl-5H-4λ4,5λ4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinine
Conditions | Yield |
---|---|
With chloro-trimethyl-silane In acetonitrile at 120℃; for 4h; Microwave irradiation; | 95% |
meso-tartaric acid
8-mesityl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
Conditions | Yield |
---|---|
With chloro-trimethyl-silane In acetonitrile at 120℃; for 8h; Microwave irradiation; | 95% |
vortioxetine
meso-tartaric acid
Conditions | Yield |
---|---|
In acetone at 20℃; for 0.5h; | 93% |
In acetone at 20℃; for 0.5h; | 93% |
methanol
meso-tartaric acid
2,2-dimethoxy-propane
dimethyl meso-2,2-dimethyl-1,3-dioxolane-4,5-dicarboxylate
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In cyclohexane for 48h; Heating; | 92% |
toluene-4-sulfonic acid |
meso-tartaric acid
1-n-butyl-3-methylimidazolim bromide
Conditions | Yield |
---|---|
Stage #1: meso-tartaric acid With silver (II) carbonate In water-d2 at 20℃; for 2h; Darkness; Stage #2: 1-n-butyl-3-methylimidazolim bromide In water-d2 at 20℃; Darkness; | 92% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene at 55℃; for 4h; Reagent/catalyst; Solvent; Temperature; | 91.2% |
Conditions | Yield |
---|---|
In hexane; isopropyl alcohol at 45 - 50℃; | 90.2% |
Conditions | Yield |
---|---|
In ethanol at 45℃; for 0.666667h; | 89.6% |
meso-tartaric acid
Conditions | Yield |
---|---|
In water stirring (+)-(.LAMDA.)-(Co(en)2(NO2)2)Br, Ag2tart, and H2tart in H2O at room temp. for 20 min; AgBr ppt. filtered, filtrate reduced to half vol., scratching surface of beaker, first crop of cryst. deposited, 2nd crop on further reducing the vol., recrystn. from hot (333°K) water, anal. by x-ray diffraction; | 89% |
methanol
meso-tartaric acid
dimethyl meso-tartrate
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene for 20h; Reflux; | 88% |
With hydrogenchloride ice bath; | 67.5% |
With thionyl chloride at 0℃; for 4h; Reflux; Inert atmosphere; | 32% |
With Amberlyst-15 |
meso-tartaric acid
Conditions | Yield |
---|---|
Stage #1: 3,3’-di-n-octyl-1,1’-(1,4-phenylenedimethylene)diimidazolium dibromide With Amberlite resin IRA-400 (hydroxide form) In methanol; water Stage #2: meso-tartaric acid In methanol; water | 86% |
meso-tartaric acid
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid at 38℃; for 24h; | 83% |
meso-tartaric acid
diazodiphenylmethane
bis(diphenylmethyl) meso-tartrate
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 82% |
In methanol; chloroform Ambient temperature; |
meso-tartaric acid
Conditions | Yield |
---|---|
In ethyl acetate at 20 - 25℃; for 16h; | 80% |
Conditions | Yield |
---|---|
Stage #1: caffeic acid With thionyl chloride In toluene for 4h; Reflux; Stage #2: meso-tartaric acid In toluene for 5h; Reflux; | 79.7% |
(R)-5-(2-oxiranyl)-8-benzyloxy-2(1H)-quinolinone
5,6-diethyl-2,3-dihydro-1H-inden-2-amine
meso-tartaric acid
Conditions | Yield |
---|---|
Stage #1: (R)-5-(2-oxiranyl)-8-benzyloxy-2(1H)-quinolinone; 5,6-diethyl-2,3-dihydro-1H-inden-2-amine In cyclohexanone at 80℃; for 6h; Stage #2: meso-tartaric acid In ethanol; cyclohexanone at 60℃; for 0.0833333h; | 78.3% |
meso-tartaric acid
(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
trimethyl orthoformate
Conditions | Yield |
---|---|
With sulfuric acid In methanol for 120h; Ambient temperature; | 76% |
meso-tartaric acid
Sr(meso-Tar)
Conditions | Yield |
---|---|
With strontium(II) acetate In water at 125℃; for 48h; Autoclave; | 76% |
meso-tartaric acid
benzylamine
(3R,4S)-1-benzyl-3,4-dihydroxypyrrolidine-2,5-dione
Conditions | Yield |
---|---|
In 5,5-dimethyl-1,3-cyclohexadiene at 190℃; for 6h; Dean-Stark; | 76% |
In para-xylene Reflux; |
meso-tartaric acid
Conditions | Yield |
---|---|
With lithium acetate dihydrate In ethanol; water at 123℃; for 144h; Temperature; Autoclave; | 76% |
Conditions | Yield |
---|---|
With per-rhenic acid In water at 170℃; for 3h; Inert atmosphere; | 75% |
Conditions | Yield |
---|---|
With rhenium oxide and palladium co-loaded on activated carbon at 109.84℃; for 24h; | 71% |
Conditions | Yield |
---|---|
With trifluoroacetic anhydride In dichloromethane at 20℃; for 12h; | 68% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene Reflux; Inert atmosphere; | 64% |
With toluene-4-sulfonic acid In benzene |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid at 100℃; for 2h; | 64% |
meso-tartaric acid
Conditions | Yield |
---|---|
In water stirring (-)-(.DELTA:)-(Co(en)2(NO2)2)Br, Ag2tart, and H2tart in H2O at room temp. for 20 min; reducing the vol. of filtrate by half twice yielded 2 crops, recrystn. from hot water; | 62% |
meso-tartaric acid
3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium bromide
Conditions | Yield |
---|---|
Stage #1: meso-tartaric acid With triethylamine In methanol under 760.051 Torr; pH=Ca. 8; Cooling with ice; Sealed tube; Stage #2: 3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium bromide In methanol under 760.051 Torr; Heating; Sealed tube; | 62% |
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