Product Name

  • Name

    beta-D-(-)-Arabinose

  • EINECS 233-708-5
  • CAS No. 10323-20-3
  • Article Data186
  • CAS DataBase
  • Density 1.757 g/cm3
  • Solubility Soluble in water.
  • Melting Point 156-160 °C
  • Formula C5H10O5
  • Boiling Point 415.462 °C at 760 mmHg
  • Molecular Weight 150.131
  • Flash Point 219.215 °C
  • Transport Information
  • Appearance White to off-white powder
  • Safety 26-36
  • Risk Codes 20/21/22-36/37/38
  • Molecular Structure Molecular Structure of 10323-20-3 (beta-D-(-)-Arabinose)
  • Hazard Symbols HarmfulXn
  • Synonyms Arabinose,D- (8CI);(-)-Arabinose;Anhydroarabinose;D-Arabinose;
  • PSA 97.99000
  • LogP -2.73970

Synthetic route

7-(tert-butyl-diphenyl-silanyloxy)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ol

7-(tert-butyl-diphenyl-silanyloxy)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ol

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
With hydrogenchloride; water at 18℃; for 18h;68%
Conditions
ConditionsYield
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
73080-26-9

5,6-dihydro-6-(S)-(1,3-dithian-2-yl)-1-β-D-arabinofuranosyluracil

A

D-Arabinose
10323-20-3

D-Arabinose

B

5,6-dihydro-6-(S)-(1,3-dithian-2-yl)uracil
73080-27-0, 76222-45-2

5,6-dihydro-6-(S)-(1,3-dithian-2-yl)uracil

Conditions
ConditionsYield
With hydrogenchloride at 70℃; for 4h;A n/a
B 62%
deacetylated Scutellaria baicalensis water-soluble polysaccharide

deacetylated Scutellaria baicalensis water-soluble polysaccharide

A

D-Arabinose
10323-20-3

D-Arabinose

B

D-glucose
50-99-7

D-glucose

C

D-Galactose
59-23-4

D-Galactose

D

partially hydrolysed deacetylated Scutellaria baicalensis water-soluble polysaccharide

partially hydrolysed deacetylated Scutellaria baicalensis water-soluble polysaccharide

E

galactobiose

galactobiose

Conditions
ConditionsYield
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
50-69-1

D-ribose

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
With molybdic acid In water for 0.05h; Bilik reaction; microwave irradiation;45%
2-C-(hydroxymethyl)-D-glycero-D-gulo-heptose
367261-89-0

2-C-(hydroxymethyl)-D-glycero-D-gulo-heptose

A

D-Arabinose
10323-20-3

D-Arabinose

B

dihydroxyacetone
96-26-4

dihydroxyacetone

C

D-glycero-D-ido-oct-2-ulose
1016606-96-4

D-glycero-D-ido-oct-2-ulose

Conditions
ConditionsYield
With molybdic acid In water at 85℃; for 8h;A n/a
B n/a
C 40%
pyridine
110-86-1

pyridine

D-ribulose
488-84-6

D-ribulose

A

D-Arabinose
10323-20-3

D-Arabinose

B

D-ribose
50-69-1

D-ribose

pyridine
110-86-1

pyridine

xylulose
551-84-8

xylulose

A

D-xylose
58-86-6

D-xylose

B

D-Arabinose
10323-20-3

D-Arabinose

C

D-ribose
50-69-1

D-ribose

mannitol
69-65-8

mannitol

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
With lead(IV) acetate; oxalic acid; acetic acid Erwaermen des Reaktionsprodukts mit Wasser;
With periodic acid
D-arabinonic acid methyl ester
15909-68-9

D-arabinonic acid methyl ester

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
With sodium amalgam; sulfuric acid; water
2-amino-2-deoxyglucose
3416-24-8

2-amino-2-deoxyglucose

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
With sodium hypochlorite; water
With water; chloroamine-T
D-glucose
50-99-7

D-glucose

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
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;
D-glucose
50-99-7

D-glucose

A

D-Arabinose
10323-20-3

D-Arabinose

B

arabinoic acid
488-30-2

arabinoic acid

Conditions
ConditionsYield
With sulfuric acid Elektrolyse an Bleianoden;
D-mannose diethyl dithioacetal
6748-69-2

D-mannose diethyl dithioacetal

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
With 1,4-dioxane; perpropionic acid Behandeln des Reaktionsprodukts mit wss.Ammoniak;
1-Desoxy-1-nitro-D-arabino-pentitol
55065-39-9

1-Desoxy-1-nitro-D-arabino-pentitol

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
With sodium hydroxide anschliessendes Behandeln mit wss.Schwefelsaeure;
D-gluconamide
3118-85-2

D-gluconamide

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
With sodium hypochlorite
gluconic acid
526-95-4

gluconic acid

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
Einw. von anderen Oxydationsmitteln;
D-glucose oxime
608-81-1

D-glucose oxime

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
With sodium hydrogencarbonate anschliessendes Erwaermen mit 1-Fluor-2,4-dinitro-benzol in Isopropylalkohol;
D-arabino-3,4,5,6-tetraacetoxy-1,1-bis-ethanesulfonyl-hex-1-ene
109454-90-2, 109785-30-0

D-arabino-3,4,5,6-tetraacetoxy-1,1-bis-ethanesulfonyl-hex-1-ene

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
With methanol; water; hydrazine Erwaermen einer wss.Loesung des Reaktionsprodukts mit Benzaldehyd,wenig Benzoesaeure und Aethanol;
chloroform
67-66-3

chloroform

2,3,4,5,6-penta-O-benzoyl-D-glucononitrile
29505-20-2

2,3,4,5,6-penta-O-benzoyl-D-glucononitrile

sodium methylate
124-41-4

sodium methylate

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
at -5℃;
chloroform
67-66-3

chloroform

1,2,3,4,5-penta-O-benzoyl-D-mannonic acid nitrile
71439-41-3

1,2,3,4,5-penta-O-benzoyl-D-mannonic acid nitrile

sodium methylate
124-41-4

sodium methylate

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
at -5℃;
2,2:4,5-di-O-isopropylidene-D-arabinose
13039-93-5

2,2:4,5-di-O-isopropylidene-D-arabinose

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
With sulfuric acid
avicularin
572-30-5

avicularin

A

D-Arabinose
10323-20-3

D-Arabinose

B

quercetol
117-39-5

quercetol

Conditions
ConditionsYield
With hydrogenchloride for 2h; Heating;
D-Mannose
3458-28-4

D-Mannose

A

D-Arabinose
10323-20-3

D-Arabinose

B

D-erythrose
583-50-6

D-erythrose

Conditions
ConditionsYield
With iron(III) chloride In water at 20℃; for 3h; Product distribution; Irradiation;
D-Mannose
3458-28-4

D-Mannose

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
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;
D-glucose
50-99-7

D-glucose

A

D-Glyceraldehyde
453-17-8

D-Glyceraldehyde

B

D-Arabinose
10323-20-3

D-Arabinose

C

D-erythrose
583-50-6

D-erythrose

Conditions
ConditionsYield
With iron(III) chloride In water at 20℃; for 3h; Product distribution; Kinetics; Mechanism; Irradiation; various reaction times.;
D-arabinopyranose
28697-53-2

D-arabinopyranose

D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
With potassium chloride In water at 25℃; Equilibrium constant; Thermodynamic data; free energy of cyclization ΔG0c;
dimorphoside A
108179-46-0

dimorphoside A

A

D-Arabinose
10323-20-3

D-Arabinose

B

D-glucose
50-99-7

D-glucose

Conditions
ConditionsYield
With hydrogenchloride In methanol; water Product distribution; Heating; products ratio 1:1;
D-Arabinose
10323-20-3

D-Arabinose

phenylboronic acid
98-80-6

phenylboronic acid

C17H16B2O5
1218927-63-9

C17H16B2O5

Conditions
ConditionsYield
In methanol; water at 20℃; for 2h;100%
Conditions
ConditionsYield
In methanol at 20 - 45℃; for 3h;100%
methanol
67-56-1

methanol

D-Arabinose
10323-20-3

D-Arabinose

(2S,3R,4R)-2-(hydroxymethyl)-5-methoxytetrahydrofuran-3,4-diol
13039-64-0

(2S,3R,4R)-2-(hydroxymethyl)-5-methoxytetrahydrofuran-3,4-diol

Conditions
ConditionsYield
With hydrogenchloride; acetyl chloride at 0 - 20℃; for 3h;100%
With acetyl chloride at 0 - 20℃; for 3h;100%
D-Arabinose
10323-20-3

D-Arabinose

ethanethiol
75-08-1

ethanethiol

D-arabinose diethyl dithioacetal
1941-50-0

D-arabinose diethyl dithioacetal

Conditions
ConditionsYield
With hydrogenchloride; zinc(II) chloride99%
In hydrogenchloride at 0℃; for 0.5h;91%
88%
D-Arabinose
10323-20-3

D-Arabinose

acetylacetone
123-54-6

acetylacetone

1-((2S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)propan-2-one

1-((2S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)propan-2-one

Conditions
ConditionsYield
With sodium carbonate In water at 10℃; for 12h; stereoselective reaction;97%
D-Arabinose
10323-20-3

D-Arabinose

4-Chloro-1,2-phenylenediamine
95-83-0

4-Chloro-1,2-phenylenediamine

(1R,2S,3R)-2-(1,2,3,4-tetrahydroxybutyl)-1H-6-chlorobenzimidazole
1609208-14-1

(1R,2S,3R)-2-(1,2,3,4-tetrahydroxybutyl)-1H-6-chlorobenzimidazole

Conditions
ConditionsYield
With iodine In water; acetic acid at 20℃; for 3h;97%
D-Arabinose
10323-20-3

D-Arabinose

2,3-Diaminonaphthalene
771-97-1

2,3-Diaminonaphthalene

(1'R,2'S,3'R,)-2-[1',2',3',4'-tetrahydroxybutyl]-1H-naphthimidazole
1027103-25-8

(1'R,2'S,3'R,)-2-[1',2',3',4'-tetrahydroxybutyl]-1H-naphthimidazole

Conditions
ConditionsYield
With air; iodine; acetic acid at 20℃; for 3h;96%
D-Arabinose
10323-20-3

D-Arabinose

phosphoenolpyruvate trianion
67533-07-7

phosphoenolpyruvate trianion

D-arabinose-5-phosphate

D-arabinose-5-phosphate

Conditions
ConditionsYield
With sodium hydroxide; pyruvate kinase; potassium chloride; magnesium sulfate; 2-hydroxyethanethiol; hexokinase In water at 20℃; for 46h; pH=7.6; Enzymatic reaction;95%
carbonic acid bis(1-isopropylhydrazide) dihydrochloride

carbonic acid bis(1-isopropylhydrazide) dihydrochloride

D-Arabinose
10323-20-3

D-Arabinose

1'R,2'S,3'R-2,4-diisopropyl-6-(1',2',3',4'-tetrahydroxybutyl)-1,2,4,5-tetrazinan-3-one

1'R,2'S,3'R-2,4-diisopropyl-6-(1',2',3',4'-tetrahydroxybutyl)-1,2,4,5-tetrazinan-3-one

Conditions
ConditionsYield
With sodium acetate In water at 20℃;95%
methanol
67-56-1

methanol

D-Arabinose
10323-20-3

D-Arabinose

methyl D-arabinofuranoside
79083-42-4

methyl D-arabinofuranoside

Conditions
ConditionsYield
With hydrogenchloride at 20℃; for 5h;94%
With acetyl chloride at 20℃; for 18h;91%
With acetyl chloride for 24h; Inert atmosphere;82%
D-Arabinose
10323-20-3

D-Arabinose

phenylmethanethiol
100-53-8

phenylmethanethiol

L-(+)-arabinose dibenzyl thioacetal
34685-26-2

L-(+)-arabinose dibenzyl thioacetal

Conditions
ConditionsYield
In hydrogenchloride for 0.5h;93%
With hydrogenchloride; zinc(II) chloride81%
With hydrogenchloride
With hydrogenchloride; zinc(II) chloride
With trifluoroacetic acid
D-Arabinose
10323-20-3

D-Arabinose

6-hydrazino-1,3-dimethyl-1H-pyrimidine-2,4-dione
123506-40-1

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
69471-90-5

1,3-Dimethyl-6-{N'-[(2R,3S,4R)-2,3,4,5-tetrahydroxy-pent-(Z)-ylidene]-hydrazino}-1H-pyrimidine-2,4-dione

Conditions
ConditionsYield
In methanol for 5h; Heating;93%
D-Arabinose
10323-20-3

D-Arabinose

4-hydrazino-1,3-diphenylpyrazolo[3,4-d]pyrimidine
1082607-20-2

4-hydrazino-1,3-diphenylpyrazolo[3,4-d]pyrimidine

D-arabinose N-(1,3-diphenylpyrazolo[3,4-d]pyrimidin-4-y)hydrazone

D-arabinose N-(1,3-diphenylpyrazolo[3,4-d]pyrimidin-4-y)hydrazone

Conditions
ConditionsYield
With hydrogenchloride In ethanol; water for 6h; Reflux;93%
D-Arabinose
10323-20-3

D-Arabinose

N-Phenyl-N'-thiobenzoyl-hydrazin
13437-75-7

N-Phenyl-N'-thiobenzoyl-hydrazin

(1S,2R,3R)-1-<(2S)-(3,5-diphenyl-2,3-dihydro-<1,3,4>thiadiazol-2-yl)>-butane-1,2,3,4-tetraol

(1S,2R,3R)-1-<(2S)-(3,5-diphenyl-2,3-dihydro-<1,3,4>thiadiazol-2-yl)>-butane-1,2,3,4-tetraol

Conditions
ConditionsYield
With hydrogenchloride In ethanol at 20℃; for 3h;92%
D-Arabinose
10323-20-3

D-Arabinose

furfural
98-01-1

furfural

Conditions
ConditionsYield
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
10323-20-3

D-Arabinose

4,5-dimethyl-1,2-phenylenediamine
3171-45-7

4,5-dimethyl-1,2-phenylenediamine

(1'R,2'S,3'R)-5,6-dimethyl-2-[1',2',3',4'-tetrahydroxybutyl]-1H-benzimidazole

(1'R,2'S,3'R)-5,6-dimethyl-2-[1',2',3',4'-tetrahydroxybutyl]-1H-benzimidazole

Conditions
ConditionsYield
With iodine In water; acetic acid at 20℃; for 3.5h;92%
With iodine; acetic acid In methanol at 20℃; for 12h;
D-Arabinose
10323-20-3

D-Arabinose

C19H20N4O2
876594-46-6

C19H20N4O2

1-[4-(2-methoxybenzyl)-6-(4-methoxyphenyl)-2H-pyridazin-3-ylidene]-2-(pent-1-ylidene-2,3,4,5-tetraol) hydrazine
1155315-21-1

1-[4-(2-methoxybenzyl)-6-(4-methoxyphenyl)-2H-pyridazin-3-ylidene]-2-(pent-1-ylidene-2,3,4,5-tetraol) hydrazine

Conditions
ConditionsYield
In ethanol for 5h; Reflux;92%
L-Cysteine
52-90-4

L-Cysteine

D-Arabinose
10323-20-3

D-Arabinose

C8H14NO6S(1-)*Na(1+)

C8H14NO6S(1-)*Na(1+)

Conditions
ConditionsYield
With sodium hydroxide at 80℃; pH=9.5; Temperature; Flow reactor;92%
4-Butylaniline
104-13-2

4-Butylaniline

D-Arabinose
10323-20-3

D-Arabinose

4-butyl-N,N-bis(d-arabinityl)aniline

4-butyl-N,N-bis(d-arabinityl)aniline

Conditions
ConditionsYield
With sodium cyanoborohydride; acetic acid In methanol at 50℃; for 24h;92%
D-Arabinose
10323-20-3

D-Arabinose

Conditions
ConditionsYield
With sodium borodeuteride; potassium hydrogencarbonate In water for 24h;91%
With sodium borodeuteride at 4℃;
D-Arabinose
10323-20-3

D-Arabinose

acetic anhydride
108-24-7

acetic anhydride

p-toluidine
106-49-0

p-toluidine

acetylacetone
123-54-6

acetylacetone

(6S)-3-acetyl-2-methyl-1-(4-methylphenyl)-1,5,6,7-tetrahydropyrano[3,2-b]pyrrol-6-yl acetate
1020540-90-2

(6S)-3-acetyl-2-methyl-1-(4-methylphenyl)-1,5,6,7-tetrahydropyrano[3,2-b]pyrrol-6-yl acetate

Conditions
ConditionsYield
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
10323-20-3

D-Arabinose

acetic anhydride
108-24-7

acetic anhydride

benzo[1,3]dioxolo-5-ylamine
14268-66-7

benzo[1,3]dioxolo-5-ylamine

acetylacetone
123-54-6

acetylacetone

(6S)-3-acetyl-1-(1,3-benzodioxol-5-yl)-2-methyl-1,5,6,7-tetrahydropyrano[3,2-b]pyrrol-6-yl acetate
1020540-92-4

(6S)-3-acetyl-1-(1,3-benzodioxol-5-yl)-2-methyl-1,5,6,7-tetrahydropyrano[3,2-b]pyrrol-6-yl acetate

Conditions
ConditionsYield
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
10323-20-3

D-Arabinose

D-arabinono-1,4-lactone
2782-09-4

D-arabinono-1,4-lactone

Conditions
ConditionsYield
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
10323-20-3

D-Arabinose

hydrazinecarbodithioic acid methyl ester
5397-03-5

hydrazinecarbodithioic acid methyl ester

N'-[(2R,3S,4R)-2,3,4,5-Tetrahydroxy-pent-(E)-ylidene]-hydrazinecarbodithioic acid methyl ester

N'-[(2R,3S,4R)-2,3,4,5-Tetrahydroxy-pent-(E)-ylidene]-hydrazinecarbodithioic acid methyl ester

Conditions
ConditionsYield
In methanol; water for 0.166667h; Heating;90%
D-Arabinose
10323-20-3

D-Arabinose

2-hydrazineyl-6-phenylpyrimidin-4(3H)-one
86799-26-0

2-hydrazineyl-6-phenylpyrimidin-4(3H)-one

6-Phenyl-2-{N'-[(2R,3S,4R)-2,3,4,5-tetrahydroxy-pent-(E)-ylidene]-hydrazino}-3H-pyrimidin-4-one

6-Phenyl-2-{N'-[(2R,3S,4R)-2,3,4,5-tetrahydroxy-pent-(E)-ylidene]-hydrazino}-3H-pyrimidin-4-one

Conditions
ConditionsYield
In ethanol; water for 0.25h; Condensation; Heating;90%
6-Amino-2-thiouracil
1004-40-6

6-Amino-2-thiouracil

D-Arabinose
10323-20-3

D-Arabinose

chloroacetic acid
79-11-8

chloroacetic acid

7-amino-2-arabinosyl-2,3-dihydro-5H-thiazolo[3,2-a]pyrimidine-3,5-dione

7-amino-2-arabinosyl-2,3-dihydro-5H-thiazolo[3,2-a]pyrimidine-3,5-dione

Conditions
ConditionsYield
With piperidine; pyridine for 8h; Reflux;90%
2-hydrazinyl-4-methylquinoline
21703-52-6

2-hydrazinyl-4-methylquinoline

D-Arabinose
10323-20-3

D-Arabinose

(2R,3S,4R)-5-[(4-Methyl-quinolin-2-yl)-hydrazono]-pentane-1,2,3,4-tetraol

(2R,3S,4R)-5-[(4-Methyl-quinolin-2-yl)-hydrazono]-pentane-1,2,3,4-tetraol

Conditions
ConditionsYield
With acetic acid In ethanol for 0.5h; Heating;89%
D-Arabinose
10323-20-3

D-Arabinose

benzoyl chloride
98-88-4

benzoyl chloride

1,2,3,4-tetra-O-benzoyl-D-arabinopyranose
377075-27-9

1,2,3,4-tetra-O-benzoyl-D-arabinopyranose

Conditions
ConditionsYield
With pyridine; dmap at 0 - 20℃; for 24h;89%
D-Arabinose
10323-20-3

D-Arabinose

benzyl alcohol
100-51-6

benzyl alcohol

(-)-benzyl β-D-arabinopyranoside
5329-50-0

(-)-benzyl β-D-arabinopyranoside

Conditions
ConditionsYield
With acetyl chloride In tert-butyl methyl ether at 35 - 50℃;88.6%
With hydrogenchloride
D-Arabinose
10323-20-3

D-Arabinose

5-ethyl-3-hydrazino-5H-1,2,4-triazino<5,6-b>indole
49830-45-7

5-ethyl-3-hydrazino-5H-1,2,4-triazino<5,6-b>indole

D-arabinose 5-ethyl-1,2,4-triazino[5,6-b]indol-3-ylhydrazone

D-arabinose 5-ethyl-1,2,4-triazino[5,6-b]indol-3-ylhydrazone

Conditions
ConditionsYield
In ethanol; water for 0.25h; Condensation; Heating;88%

D-(-)-Arabinose Chemical Properties

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

D-(-)-Arabinose Safety Profile

Safety Information of D-(-)-Arabinose  (CAS NO.10323-20-3):
Hazard Codes: HarmfulXn
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 Specification

 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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