Henan 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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Cas:473-90-5
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
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
hight degree of purity Application:Fine chemical intermediates, used as the main raw material for he synthesis of various pesticides, medicines, surfactants, polymer monomers, Ond Ontifungal agents
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Compound sourcing ServicesAgency of testing serviceFactory audit serviceFounded in Dec. 1999, Nanjing Chemlin Chemical Industrial Co.,Ltd(CHEMLIN) has been covering the business scope from trading of chemicals to custom-synthesis & Manufacturing. Co
FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the Oxomalonic acid, CAS:473-90-5 with the most competitive price and the best quality. W
1,3-dihydroxyacetone dimer
A
acetonedicarboxylic acid
B
acetaldehyde
C
acetone
D
2-oxopropanal
Conditions | Yield |
---|---|
bei mehrjaehrigem Aufbewahren eines Handelspraeparats unter Ausschluss von Licht und Luft; Prod.5: Milchsaeure; |
Conditions | Yield |
---|---|
With Fructose 1,6-bisphosphate; oxidized form of nicotineamide adenine dinucleotide In water at 25℃; Rate constant; pH 8.5, reaction in the presence of L-lactate dehydrogenase from Bacillus stearothermophilus (BSLDH 102R); | |
With dihydrogen peroxide; iron(II) | |
Electrolysis.Elektrolyse an Platin-Anoden in saurer Loesung; | |
With alkaline copper solution | |
With tempamine; recombinant oxalate decarboxylase from Bacillus subtilis In aq. phosphate buffer at 25℃; pH=5.2; Electrochemical reaction; Enzymatic reaction; |
pyrimidine-2,4,5,6(1H,3H)-tetraone
acetonedicarboxylic acid
Conditions | Yield |
---|---|
With acetate_of lead |
Conditions | Yield |
---|---|
With water; iodine |
(R,R)-(+)-tartaric acid monoamide
acetonedicarboxylic acid
Conditions | Yield |
---|---|
With sodium hypochlorite |
Conditions | Yield |
---|---|
Electrolysis.Elektrolyse an Platin-Anoden in saurer Loesung; | |
Electrolysis.Elektrolyse an Nickel- oder Kupfer-Anoden in alkal. Loesung; |
Conditions | Yield |
---|---|
at 65℃; |
Conditions | Yield |
---|---|
With water; copper (I) acetate at 65℃; |
Conditions | Yield |
---|---|
With silver(l) oxide |
Conditions | Yield |
---|---|
With barium dihydroxide | |
With sodium hydroxide; water Erwaermen auf dem Wasserbad; | |
With alkali |
Conditions | Yield |
---|---|
With nitric acid |
Conditions | Yield |
---|---|
With water; mercury(II) oxide |
Conditions | Yield |
---|---|
With sodium hypoiodite; water |
Conditions | Yield |
---|---|
With acetic acid ester; ozone Zersetzung des Ozonids mit kaltem Wasser; |
(5-oxo-dihydro-[2]furylidene)-malonic acid diethyl ester
A
succinic acid
B
acetonedicarboxylic acid
Conditions | Yield |
---|---|
bei der Ozonspaltung; |
4,5-dihydroxy-2-oxo-5-ureido-imidazolidine-4-carboxylic acid
acetonedicarboxylic acid
Conditions | Yield |
---|---|
With sulfuric acid; sodium nitrite Bei Zimmertemperatur; |
Conditions | Yield |
---|---|
Behandeln mit Ozon in Essigester und Zersetzen des erhaltenen Ozonids; |
acetonedicarboxylic acid
2-benzylidenemalonic acid
ethyl acetate
A
acetonedicarboxylic acid
B
benzaldehyde
C
benzoic acid
Conditions | Yield |
---|---|
at -20℃; bei der Ozonisierung nachfolgend Spaltung mit Wasser; |
Conditions | Yield |
---|---|
With bismuth(III) nitrate |
Conditions | Yield |
---|---|
With mixture of gaseous nitrogen oxides at 0℃; Extraktion des erhaltenen Oels mit kaltem Wasser und Einengen der wss. Loesung im Vakuum ueber Schwefelsaeure; |
Conditions | Yield |
---|---|
With nitric acid at 72 - 75℃; |
4-Carboxy-2.3.5.6-tetrahydroxy-4-hydroxymethyl-hepta-2,5-dien-disaeure
acetonedicarboxylic acid
Conditions | Yield |
---|---|
With hydrogenchloride; iodine |
Conditions | Yield |
---|---|
With potassium bromate In perchloric acid; acetic acid at 50℃; Thermodynamic data; Kinetics; Rate constant; mechanism; Ea, ΔH(excit.), ΔS(excit.), ΔG(excit.); var. temperatures; | |
With (15-amino-3-methyl-4,7,10,13-tetra-azapentadec-3-en-2-one oximato)nickel(III) perchlorate In water at 40℃; Rate constant; Mechanism; pH 3.0-5.75; |
Conditions | Yield |
---|---|
With oxygen In water at 25℃; Thermodynamic data; E(excit.), effects of pH, effects of O2; |
Conditions | Yield |
---|---|
With oxygen; dinitrogen monoxide In water Product distribution; Rate constant; Mechanism; Irradiation; pulse radiolysis (60Co-γ); var. pH.: 3-10; via peroxyradical intermediate; |
malonic acid
A
tartronic acid
B
acetonedicarboxylic acid
C
1,1,2,2-Ethane-tetracarboxylic acid
D
dicarboxymethyl
Conditions | Yield |
---|---|
With 4H3N*CeH4O16S4; sulfuric acid at 25℃; Rate constant; Mechanism; deuterated analog; |
1-(5-methoxy-3-methylhydantoin-5-carbonyl)-3-methylurea
acetonedicarboxylic acid
Conditions | Yield |
---|---|
With iron sulfide; ammonium carbonate In water at 100℃; for 144h; | 86% |
1,2,3,4-tetrahydroisoquinoline
acetonedicarboxylic acid
3,4-Dihydro-1H-isoquinoline-2-carbothioaldehyde
Conditions | Yield |
---|---|
With sulfur In benzene at 80℃; for 0.25h; | 80% |
acetonedicarboxylic acid
pulegone
3-Hydroxy-4,4,7-trimethyl-2-oxo-3,4,5,6,7,8-hexahydro-2H-chromene-3-carboxylic acid ethyl ester
Conditions | Yield |
---|---|
With titanium tetrachloride; magnesium In tetrahydrofuran for 8h; Ambient temperature; | 60% |
acetonedicarboxylic acid
benzaldehyde
cis-2,6-diphenyltetrahydro-4H-pyran-4-one
Conditions | Yield |
---|---|
With acid at -10℃; | 35% |
Conditions | Yield |
---|---|
Stage #1: copper (II) carbonate hydroxide; acetonedicarboxylic acid; water at 40℃; for 0.333333h; Stage #2: zinc acetate hydrate; tetraphenylphosphonium bromide In methanol at 21℃; for 168h; | 30% |
Mn(CH3COO)2·H2O
acetonedicarboxylic acid
water
tetraphenylphosphonium bromide
Conditions | Yield |
---|---|
Stage #1: copper (II) carbonate hydroxide; acetonedicarboxylic acid; water at 40℃; for 0.333333h; Stage #2: Mn(CH3COO)2·H2O; tetraphenylphosphonium bromide In methanol at 21℃; for 168h; | 30% |
Conditions | Yield |
---|---|
Stage #1: copper (II) carbonate hydroxide; acetonedicarboxylic acid; water at 40℃; for 0.333333h; Stage #2: cobalt(II) acetate monohydrate; tetraphenylphosphonium bromide In methanol at 21℃; for 168h; | 30% |
acetonedicarboxylic acid
benzaldehyde
trans-2,6-diphenyltetrahydro-4H-pyran-4-one
Conditions | Yield |
---|---|
Ambient temperature; | 21% |
trans-{CoCl2(3,7-diaza-1,9-diaminononane)}ClO4
acetonedicarboxylic acid
Conditions | Yield |
---|---|
With triethylamine In methanol refluxed for 4 h; evapn. to dryness, dissolved in water, exchange column chromy. (Sephadex, aq. NaClO4), collected, concd.; elem. anal.; | 9% |
With (C2H5)3N In methanol reflux for 4 h; mixture is evapd. to dryness, H2O is added and evapd., the mixture is dissolved in H2O and adsorbed onto SP-Sephadex C-25 column, the column is washed with H2O and eluted with NaClO4, elem. anal.; | 9% |
acetonedicarboxylic acid
para-xylene
(2,5-dimethyl-phenyl)-hydroxy-malonic acid diethyl ester
Conditions | Yield |
---|---|
With tin(IV) chloride |
acetonedicarboxylic acid
phenylhydrazine hydrochloride
2-(phenylhydrazono)malonic acid
Conditions | Yield |
---|---|
With water | |
With acid |
acetonedicarboxylic acid
o-phenylenediamine hydrochloride
3,4-Dihydro-3-oxo-2-quinoxalinecarboxylic acid
Conditions | Yield |
---|---|
With water |
acetonedicarboxylic acid
4-Methyl-benzene-1,2-diamine; hydrochloride
7-methyl-3-oxo-3,4-dihydro-quinoxaline-2-carboxylic acid
Conditions | Yield |
---|---|
With water |
Conditions | Yield |
---|---|
With sodium amalgam | |
With fructose 1,6-bisphosphate trisodium; nicotinamide adenine dinucleotide red. form; R171W mutant In water at 25℃; Rate constant; other mutant enzyme; |
Conditions | Yield |
---|---|
With alkaline permanganate |
Conditions | Yield |
---|---|
With water at 100℃; | |
With tempamine; recombinant oxalate decarboxylase from Bacillus subtilis In aq. phosphate buffer at 25℃; pH=5.2; Electrochemical reaction; Enzymatic reaction; |
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