D-Arabinose
Conditions | Yield |
---|---|
With hydrogenchloride; water at 18℃; for 18h; | 68% |
Conditions | Yield |
---|---|
With dihydrogen peroxide; FAU(2.4); copper In water at 19.85℃; for 3.5h; pH=6.5; Product distribution; Further Variations:; Catalysts; Ruff degradation; | A 63% B 9% |
5,6-dihydro-6-(S)-(1,3-dithian-2-yl)-1-β-D-arabinofuranosyluracil
A
D-Arabinose
B
5,6-dihydro-6-(S)-(1,3-dithian-2-yl)uracil
Conditions | Yield |
---|---|
With hydrogenchloride at 70℃; for 4h; | A n/a B 62% |
Conditions | Yield |
---|---|
With sulfuric acid; water at 100℃; for 0.0833333h; | A n/a B n/a C n/a D 56.2% E n/a |
D-ribose
D-Arabinose
Conditions | Yield |
---|---|
With molybdic acid In water for 0.05h; Bilik reaction; microwave irradiation; | 45% |
2-C-(hydroxymethyl)-D-glycero-D-gulo-heptose
A
D-Arabinose
B
dihydroxyacetone
C
D-glycero-D-ido-oct-2-ulose
Conditions | Yield |
---|---|
With molybdic acid In water at 85℃; for 8h; | A n/a B n/a C 40% |
mannitol
D-Arabinose
Conditions | Yield |
---|---|
With lead(IV) acetate; oxalic acid; acetic acid Erwaermen des Reaktionsprodukts mit Wasser; | |
With periodic acid |
D-arabinonic acid methyl ester
D-Arabinose
Conditions | Yield |
---|---|
With sodium amalgam; sulfuric acid; water |
2-amino-2-deoxyglucose
D-Arabinose
Conditions | Yield |
---|---|
With sodium hypochlorite; water | |
With water; chloroamine-T |
D-glucose
D-Arabinose
Conditions | Yield |
---|---|
With water; bromine; barium benzoate Erwaermen des Reaktionsprodukts mit Calciumcarbonat und Wasser und anschliessend mit wss.Wasserstoffperoxid unter Zusatz von Bariumacetat und Eisen(II)-sulfat; | |
With sodium hypochlorite; water anfangs bei pH 11,zuletzt bei pH 5; | |
With perchloric acid; ammonium vanadate In water at 50℃; under 750.06 Torr; Rate constant; Mechanism; activation volume; further pressures; | |
With cerium(IV) perchlorate In perchloric acid at 25 - 50℃; Kinetics; Product distribution; variation of the concentration; |
Conditions | Yield |
---|---|
With sulfuric acid Elektrolyse an Bleianoden; |
D-mannose diethyl dithioacetal
D-Arabinose
Conditions | Yield |
---|---|
With 1,4-dioxane; perpropionic acid Behandeln des Reaktionsprodukts mit wss.Ammoniak; |
1-Desoxy-1-nitro-D-arabino-pentitol
D-Arabinose
Conditions | Yield |
---|---|
With sodium hydroxide anschliessendes Behandeln mit wss.Schwefelsaeure; |
D-gluconamide
D-Arabinose
Conditions | Yield |
---|---|
With sodium hypochlorite |
gluconic acid
D-Arabinose
Conditions | Yield |
---|---|
Einw. von anderen Oxydationsmitteln; |
D-glucose oxime
D-Arabinose
Conditions | Yield |
---|---|
With sodium hydrogencarbonate anschliessendes Erwaermen mit 1-Fluor-2,4-dinitro-benzol in Isopropylalkohol; |
Conditions | Yield |
---|---|
anschliessend Behandeln mit Wasser; |
D-arabino-3,4,5,6-tetraacetoxy-1,1-bis-ethanesulfonyl-hex-1-ene
D-Arabinose
Conditions | Yield |
---|---|
With methanol; water; hydrazine Erwaermen einer wss.Loesung des Reaktionsprodukts mit Benzaldehyd,wenig Benzoesaeure und Aethanol; |
chloroform
2,3,4,5,6-penta-O-benzoyl-D-glucononitrile
sodium methylate
D-Arabinose
Conditions | Yield |
---|---|
at -5℃; |
chloroform
1,2,3,4,5-penta-O-benzoyl-D-mannonic acid nitrile
sodium methylate
D-Arabinose
Conditions | Yield |
---|---|
at -5℃; |
2,2:4,5-di-O-isopropylidene-D-arabinose
D-Arabinose
Conditions | Yield |
---|---|
With sulfuric acid |
Conditions | Yield |
---|---|
With hydrogenchloride for 2h; Heating; |
Conditions | Yield |
---|---|
With iron(III) chloride In water at 20℃; for 3h; Product distribution; Irradiation; |
D-Mannose
D-Arabinose
Conditions | Yield |
---|---|
With perchloric acid; ammonium vanadate In water at 55℃; under 750.06 Torr; Rate constant; Mechanism; activation volume; further pressures; | |
With cerium(IV) perchlorate In perchloric acid at 25 - 50℃; Kinetics; Product distribution; variation of the concentration; |
Conditions | Yield |
---|---|
With iron(III) chloride In water at 20℃; for 3h; Product distribution; Kinetics; Mechanism; Irradiation; various reaction times.; |
D-arabinopyranose
D-Arabinose
Conditions | Yield |
---|---|
With potassium chloride In water at 25℃; Equilibrium constant; Thermodynamic data; free energy of cyclization ΔG0c; |
Conditions | Yield |
---|---|
With hydrogenchloride In methanol; water Product distribution; Heating; products ratio 1:1; |
Conditions | Yield |
---|---|
In methanol; water at 20℃; for 2h; | 100% |
D-Arabinose
benzylamine
N-Benzyl-D-arabinosylamin
Conditions | Yield |
---|---|
In methanol at 20 - 45℃; for 3h; | 100% |
methanol
D-Arabinose
(2S,3R,4R)-2-(hydroxymethyl)-5-methoxytetrahydrofuran-3,4-diol
Conditions | Yield |
---|---|
With hydrogenchloride; acetyl chloride at 0 - 20℃; for 3h; | 100% |
With acetyl chloride at 0 - 20℃; for 3h; | 100% |
Conditions | Yield |
---|---|
With hydrogenchloride; zinc(II) chloride | 99% |
In hydrogenchloride at 0℃; for 0.5h; | 91% |
88% |
D-Arabinose
acetylacetone
Conditions | Yield |
---|---|
With sodium carbonate In water at 10℃; for 12h; stereoselective reaction; | 97% |
D-Arabinose
4-Chloro-1,2-phenylenediamine
(1R,2S,3R)-2-(1,2,3,4-tetrahydroxybutyl)-1H-6-chlorobenzimidazole
Conditions | Yield |
---|---|
With iodine In water; acetic acid at 20℃; for 3h; | 97% |
D-Arabinose
2,3-Diaminonaphthalene
(1'R,2'S,3'R,)-2-[1',2',3',4'-tetrahydroxybutyl]-1H-naphthimidazole
Conditions | Yield |
---|---|
With air; iodine; acetic acid at 20℃; for 3h; | 96% |
Conditions | Yield |
---|---|
With sodium hydroxide; pyruvate kinase; potassium chloride; magnesium sulfate; 2-hydroxyethanethiol; hexokinase In water at 20℃; for 46h; pH=7.6; Enzymatic reaction; | 95% |
D-Arabinose
Conditions | Yield |
---|---|
With sodium acetate In water at 20℃; | 95% |
Conditions | Yield |
---|---|
With hydrogenchloride at 20℃; for 5h; | 94% |
With acetyl chloride at 20℃; for 18h; | 91% |
With acetyl chloride for 24h; Inert atmosphere; | 82% |
Conditions | Yield |
---|---|
In hydrogenchloride for 0.5h; | 93% |
With hydrogenchloride; zinc(II) chloride | 81% |
With hydrogenchloride | |
With hydrogenchloride; zinc(II) chloride | |
With trifluoroacetic acid |
D-Arabinose
6-hydrazino-1,3-dimethyl-1H-pyrimidine-2,4-dione
1,3-Dimethyl-6-{N'-[(2R,3S,4R)-2,3,4,5-tetrahydroxy-pent-(Z)-ylidene]-hydrazino}-1H-pyrimidine-2,4-dione
Conditions | Yield |
---|---|
In methanol for 5h; Heating; | 93% |
D-Arabinose
4-hydrazino-1,3-diphenylpyrazolo[3,4-d]pyrimidine
Conditions | Yield |
---|---|
With hydrogenchloride In ethanol; water for 6h; Reflux; | 93% |
D-Arabinose
N-Phenyl-N'-thiobenzoyl-hydrazin
Conditions | Yield |
---|---|
With hydrogenchloride In ethanol at 20℃; for 3h; | 92% |
D-Arabinose
furfural
Conditions | Yield |
---|---|
With Dowex 50Wx8-100 ion-exchange resin at 100℃; for 6h; Ionic liquid; Sealed tube; | 92% |
With silicoaluminophosphate-44 In water; toluene at 170℃; for 8h; | 63% |
With 1-butyl-3-methylimidazolium tetrachloridoferrate(III) In water; butanone at 160℃; for 3h; | 50.7% |
D-Arabinose
4,5-dimethyl-1,2-phenylenediamine
Conditions | Yield |
---|---|
With iodine In water; acetic acid at 20℃; for 3.5h; | 92% |
With iodine; acetic acid In methanol at 20℃; for 12h; |
D-Arabinose
C19H20N4O2
1-[4-(2-methoxybenzyl)-6-(4-methoxyphenyl)-2H-pyridazin-3-ylidene]-2-(pent-1-ylidene-2,3,4,5-tetraol) hydrazine
Conditions | Yield |
---|---|
In ethanol for 5h; Reflux; | 92% |
Conditions | Yield |
---|---|
With sodium hydroxide at 80℃; pH=9.5; Temperature; Flow reactor; | 92% |
Conditions | Yield |
---|---|
With sodium cyanoborohydride; acetic acid In methanol at 50℃; for 24h; | 92% |
D-Arabinose
(1RS)-<1-2H1>-D-arabinitol
Conditions | Yield |
---|---|
With sodium borodeuteride; potassium hydrogencarbonate In water for 24h; | 91% |
With sodium borodeuteride at 4℃; |
D-Arabinose
acetic anhydride
p-toluidine
acetylacetone
(6S)-3-acetyl-2-methyl-1-(4-methylphenyl)-1,5,6,7-tetrahydropyrano[3,2-b]pyrrol-6-yl acetate
Conditions | Yield |
---|---|
Stage #1: D-Arabinose; p-toluidine; acetylacetone With indium(III) chloride In water at 80℃; for 6.5h; Stage #2: acetic anhydride With dmap In dichloromethane at 20℃; for 1h; Further stages.; | 91% |
D-Arabinose
acetic anhydride
benzo[1,3]dioxolo-5-ylamine
acetylacetone
(6S)-3-acetyl-1-(1,3-benzodioxol-5-yl)-2-methyl-1,5,6,7-tetrahydropyrano[3,2-b]pyrrol-6-yl acetate
Conditions | Yield |
---|---|
Stage #1: D-Arabinose; benzo[1,3]dioxolo-5-ylamine; acetylacetone With indium(III) chloride In water at 80℃; for 6.5h; Stage #2: acetic anhydride With dmap In dichloromethane at 20℃; for 1h; Further stages.; | 91% |
D-Arabinose
D-arabinono-1,4-lactone
Conditions | Yield |
---|---|
With bromine; barium carbonate In water at 0 - 20℃; for 4.3h; Oxidation; | 90% |
With pseudomonas-saccharophila-cultures | |
With quinoprotein D-glucose dehydrogenase Enzymatic reaction; |
D-Arabinose
hydrazinecarbodithioic acid methyl ester
Conditions | Yield |
---|---|
In methanol; water for 0.166667h; Heating; | 90% |
D-Arabinose
2-hydrazineyl-6-phenylpyrimidin-4(3H)-one
Conditions | Yield |
---|---|
In ethanol; water for 0.25h; Condensation; Heating; | 90% |
Conditions | Yield |
---|---|
With piperidine; pyridine for 8h; Reflux; | 90% |
2-hydrazinyl-4-methylquinoline
D-Arabinose
Conditions | Yield |
---|---|
With acetic acid In ethanol for 0.5h; Heating; | 89% |
D-Arabinose
benzoyl chloride
1,2,3,4-tetra-O-benzoyl-D-arabinopyranose
Conditions | Yield |
---|---|
With pyridine; dmap at 0 - 20℃; for 24h; | 89% |
Conditions | Yield |
---|---|
With acetyl chloride In tert-butyl methyl ether at 35 - 50℃; | 88.6% |
With hydrogenchloride |
D-Arabinose
5-ethyl-3-hydrazino-5H-1,2,4-triazino<5,6-b>indole
Conditions | Yield |
---|---|
In ethanol; water for 0.25h; Condensation; Heating; | 88% |
Molecular Structure of D-(-)-Arabinose (CAS NO.10323-20-3):
IUPAC Name: (2S,3R,4R)-2,3,4,5-Tetrahydroxypentanal
Canonical SMILES: C(C(C(C(C=O)O)O)O)O
Isomeric SMILES: C([C@H]([C@H]([C@@H](C=O)O)O)O)O
InChI: InChI=1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4-,5+/m1/s1
InChIKey: PYMYPHUHKUWMLA-WDCZJNDASA-N
Molecular Weight: 150.1299 [g/mol]
Molecular Formula: C5H10O5
XLogP3: -2.3
H-Bond Donor: 4
H-Bond Acceptor: 5
EINECS: 233-708-5
Index of Refraction: 1.543
Molar Refractivity: 31.41 cm3
Molar Volume: 99.5 cm3
Surface Tension: 81.4 dyne/cm
Density: 1.508 g/cm3
Flash Point: 219.2 °C
Enthalpy of Vaporization: 77.23 kJ/mol
Boiling Point: 415.5 °C at 760 mmHg
Vapour Pressure: 1.22E-08 mmHg at 25 °C
Melting Point: 156-160 °C
Product Categories: CARBOHYDRATE; FINE Chemical & INTERMEDIATES; Carbohydrates; Basic Sugars (Mono & Oligosaccharides); Arabinose; Biochemistry; Sugars; Dextrins、Sugar & Carbohydrates; Base Ingredients; Carbohydrate Sources (Sugars/Extracts); Sugars for Media; Carbohydrates A to; Carbohydrates A-CBiochemicals and Reagents; Monosaccharide; CarbohydrateSpecialty Synthesis; Carbohydrate Synthesis; Metabolic Pathways; Metabolites and Cofactors on the Metabolic Pathways Chart; Monosaccharides; Biochemicals; Molecular Biology; Molecular Biology Reagents
Safety Information of D-(-)-Arabinose (CAS NO.10323-20-3):
Hazard Codes: Xn
Risk Statements: 20/21/22-36/37/38
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 26-36
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36:Wear suitable protective clothing.
WGK Germany: 3
F: 3-10
D-(-)-Arabinose (CAS NO.10323-20-3), its Synonyms are Arabinose,d ; D-Arabinose ; beta-D-(-)-Arabinose ; Pentopyranose ; D-Arabinose (9CI) .
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