D-Erythrose supplier | CasNO.583-50-6

Name
D-(-)-ERYTHROSE
EINECS 209-505-2
CAS No. 583-50-6
Article Data87
CAS DataBase
Density 1.41 g/cm³
Solubility Fully miscible in water.
Melting Point <25℃
Formula C₄H₈O₄
Boiling Point 311.1 °C at 760 mmHg
Molecular Weight 120.105
Flash Point 156.2 °C
Transport Information
Appearance clear colourless very viscous liquid
Safety 24/25-36-26
Risk Codes 36/37/38
Molecular Structure
Hazard Symbols Xi
Synonyms Butanal,2,3,4-trihydroxy-, [R-(R*,R*)]-;Erythrose, D- (8CI);D-(-)-Erythrose;D-Erythrose;
PSA 77.76000
LogP -2.10060

Synthetic route

: 57-48-7
D-Fructose

: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With sodium hydroxide; iron(III) chloride In water at 20℃; Quantum yield; Irradiation; other carbohydrate-metal ion system: D-fructose-MnCl2, D-glucose-FeCl3;	74%
With perchloric acid; ammonium vanadate In water at 30℃; under 750.06 Torr; Rate constant; Mechanism; activation volume; further pressures;

: 909878-64-4
meso-erythritol

A: 533-50-6, 35007-64-8, 40031-31-0, 496-55-9
D-erythrulose

B: 473-81-4, 600-19-1, 6000-40-4, 28305-26-2
D-glyceric acid

C: 488-16-4
D-erythronic acid

D: 583-50-6
D-erythrose

Conditions

Conditions	Yield
PtTl In perchloric acid; water for 4h; Product distribution; electrocatalytic reaction; also on Pt and on Pt-Pb electrode; oxidation potential varied: 0.45, 0.6, 0.8 V;	A 74% B n/a C 22% D n/a
platinum lead wire In perchloric acid; water for 4h; electrocatalytic reaction;	A 4% B 5% C 33% D 7%

...Expand

: 3391-82-0, 4688-50-0, 6027-86-7, 6622-52-2, 14933-21-2, 18404-69-8, 45079-02-5, 69617-74-9, 71074-87-8, 90010-62-1, 121929-17-7, 299-28-5
calcium gluconate

A: 10323-20-3
D-Arabinose

B: 583-50-6
D-erythrose

Conditions

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%

: 2-[((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-4-isopropyl-2H-oxazol-5-one

A: 759-05-7
3-methyl-2-ketobutanoic acid

B: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With hydrogenchloride In tetrahydrofuran Ambient temperature;	A n/a B 59%

: 95-43-2
D-threose

A: 533-50-6, 35007-64-8, 40031-31-0, 496-55-9
D-erythrulose

B: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With zeolite H-USY In water at 120℃; for 3h;	A 26% B 1%

: 533-50-6, 35007-64-8, 40031-31-0, 496-55-9
D-erythrulose

A: 95-43-2
D-threose

B: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With zeolite H-USY In water at 120℃; for 3h;	A 5% B 4%
With pyridine Equilibrium constant; Heating;

: 50-99-7
D-glucose

: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With lead(IV) acetate; acetic acid Erwaermen der erhaltenen O2,O3(oderO2,O4)-Diformyl-D-erythrose mit verd. wss. Salzsaeure;
With lead(IV) acetate
With molybdenum(VI) oxide In isopropyl alcohol at 190℃; for 2.66667h; Reagent/catalyst; Solvent;

: 115014-57-8
5,5-bis-ethanesulfonyl-L-erythro-pent-4-ene-1,2,3-triol

: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With ammonium hydroxide

: 34360-54-8
D-arabinononitrile 2,3,4,5-tetraacetate

: 124-41-4
sodium methylate

: 583-50-6
D-erythrose

: 901783-93-5
2,4-O-ethylidene-aldehydo-D-erythrose

A: 29810-04-6
endo-2,3-O-ethylidene-β-D-erythrofuranose

B: 77489-43-1
exo-1,2-O-ethylidene-α-D-erythrofuranose

C: 77519-84-7
exo-2,3-O-ethylidene-β-D-erythrofuranose

D: 583-50-6
D-erythrose

Conditions

Conditions	Yield
sulfuric acid for 0.25h; Heating;

...Expand

: 901783-93-5
2,4-O-ethylidene-aldehydo-D-erythrose

: 583-50-6
D-erythrose

Conditions

Conditions	Yield
In sulfuric acid at 100℃; for 0.25h; steam distillation;	11.5 g

: 57-48-7
D-Fructose

A: 453-17-8
D-Glyceraldehyde

B: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With iron(III) chloride In water at 20℃; for 2h; Product distribution; Kinetics; Mechanism; Irradiation; anaerobic and aerobic conditions; other reagent: Fe(NO3)3; various reaction times.;

: 57-48-7
D-Fructose

A: 488-81-3
Adonitol

B: 81893-52-9
(S)-3,4-dihydroxy-butyraldehyde

C: 81539-41-5
2,3-dideoxy-3-C-hydroxymethyltetrose

D: 81539-40-4, 132215-58-8
2-deoxy-2-C-hydroxymethyltetrose

E: 107-21-1
ethylene glycol

F: 583-50-6
D-erythrose

Conditions

Conditions	Yield
In water Quantum yield; Irradiation; 254-nm photolysis in deoxigenated and oxygenated solutions;

...Expand

: 14048-37-4
1,2-O-isopropylidene-D-erythrose

: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With oxonium

: 3458-28-4
D-Mannose

A: 10323-20-3
D-Arabinose

B: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With iron(III) chloride In water at 20℃; for 3h; Product distribution; Irradiation;

: 10323-20-3
D-Arabinose

: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With iron(III) chloride In water at 20℃; for 3h; Product distribution; Irradiation;

: 50-69-1
D-ribose

A: 453-17-8
D-Glyceraldehyde

B: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With iron(III) chloride In water at 20℃; for 3h; Product distribution; Irradiation;

: 50-69-1
D-ribose

: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With cerium(IV) perchlorate In perchloric acid at 25 - 50℃; Kinetics; Product distribution; variation of the concentration;

: 50-99-7
D-glucose

A: 453-17-8
D-Glyceraldehyde

B: 10323-20-3
D-Arabinose

C: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With iron(III) chloride In water at 20℃; for 3h; Product distribution; Kinetics; Mechanism; Irradiation; various reaction times.;

...Expand

: 210230-59-4
D-erythrofuranose

: 583-50-6
D-erythrose

Conditions

Conditions	Yield
In water-d2 at 60℃; Rate constant; Equilibrium constant; pH=4.0, acetate buffer;
With sodium acetate In water-d2 at 51℃; Rate constant; Kinetics;

: 77489-43-1
exo-1,2-O-ethylidene-α-D-erythrofuranose

: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With sulfuric acid at 96℃; for 4h; Product distribution; further erythrofuranoses;

: 6347-01-9
fructopyranose

A: 64-18-6
formic acid

B: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With oxygen; iron(III) chloride In water at 20℃; for 120h; Product distribution; Quantum yield; Irradiation; variation of time; pH range between 6.8-9.0;

: 527-07-1
sodium D-gluconate

A: 10323-20-3
D-Arabinose

B: 583-50-6
D-erythrose

Conditions

Conditions	Yield
In water at 25 - 40℃; for 12h; electrolysis; max. specific power consumption: 43 kWh kg-1; total current 17 A, pH 5.6; Yield given. Yields of byproduct given;

: 7512-17-6, 72-87-7, 1136-42-1, 1136-44-3, 6082-29-7, 6730-06-9, 7772-94-3, 10036-64-3, 14131-60-3, 14131-64-7, 14131-68-1, 14215-68-0, 62057-49-2, 62057-50-5, 62057-51-6, 62057-52-7, 62057-53-8, 62057-54-9, 62057-55-0, 62057-56-1, 62075-50-7, 62137-54-6, 134451-97-1, 134522-12-6, 148347-16-4
N-Acetyl-D-glucosamine

A: 473-81-4
glyceric acid

B: 488-16-4
D-erythronic acid

C: 10323-20-3
D-Arabinose

D: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With sodium hypochlorite; phosphate buffer In water at 37℃; for 6h; pH=7.4; Product distribution; Oxidation;

...Expand

: ammonium hydroxide

: 31818-58-3
1,1-bis-ethanesulfonyl-D-2,5-anhydro-1-deoxy-ribitol

A: 1070-92-4
bis(ethylsulfonyl)methane

B: 583-50-6
D-erythrose

...Expand

: 57-48-7
D-Fructose

: periodic acid

A: 50-00-0
formaldehyd

B: 79-14-1
glycolic Acid

C: 488-30-2
arabinoic acid

D: 583-50-6
D-erythrose

Conditions

Conditions	Yield
at 0℃; Produkt: Glyoxylsaeure;

...Expand

1,1-bis-acetylamino-D-1-deoxy-erythritol: 1,1-bis-acetylamino-D-1-deoxy-erythritol

: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With sulfuric acid

: 34360-54-8
D-arabinononitrile 2,3,4,5-tetraacetate

: 7664-93-9
sulfuric acid

: 583-50-6
D-erythrose

Conditions

Conditions	Yield
beim folgenden Behandeln mit Ba(OH)2 und Ag2CO3;

calcium-D arabinonate: calcium-D arabinonate

: 583-50-6
D-erythrose

Conditions

Conditions	Yield
With iron(III) sulfate; water; barium(II) acetate Erwaermen der Reaktionsloesung mit wss.Wasserstoffperoxid;

: S,S'-((4-(2-aminoethoxy)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride

: 583-50-6
D-erythrose

: S,S'-((4-(2-(bis((2S,3R)-2,3,4-trihydroxybutyl)amino)ethoxy)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride

Conditions

Conditions	Yield
Stage #1: S,S'-((4-(2-aminoethoxy)-1,2-phenylene)bis(methylene)) diethanethioate hydrochloride; D-erythrose With sodium cyanoborohydride; acetic acid In methanol at 55℃; for 6h; Stage #2: With hydrogenchloride In water pH=3;	73%

: 587880-59-9
{4-[4-(2-Aminoethoxy)phenyl]butyl}carbamic acid benzyl ester hydrochloride

: 583-50-6
D-erythrose

: 4-(4-Carboxymethylphenyl)butylamine

Conditions

Conditions	Yield
With sodium cyanoborohydride; acetic acid In methanol	72%

: 583-50-6
D-erythrose

: 100-51-6
benzyl alcohol

: 82883-31-6, 82883-32-7
benzyl α,β-D-erythroside

Conditions

Conditions	Yield
With hydrogenchloride; calcium sulfate for 24h;	66%

: 67-56-1
methanol

: 583-50-6
D-erythrose

A: 74761-31-2
D-Erythrose dimethyl acetal

B: 53109-84-5
methyl β-D-erythrofuranoside

C: 52613-15-7
methyl α-D-erythrofuranoside

Conditions

Conditions	Yield
With sulfuric acid for 30h; Ambient temperature;	A 8% B 65% C 11%
With sulfuric acid for 30h; Ambient temperature;	A 11% B 65% C 8%

...Expand

: 109-80-8
1.3-propanedithiol

: 583-50-6
D-erythrose

: 218439-29-3
D-erythrose propane-1,3-diyl dithioacetal

Conditions

Conditions	Yield
With hydrogenchloride In tetrahydrofuran Ambient temperature;	64%
With hydrogenchloride 1) 10 min., 0 deg C; 2) 30 min. at room temp.;	2.88 g

: 75-07-0
acetaldehyde

: 583-50-6
D-erythrose

: 75754-51-7, 75754-52-8, 137873-05-3, 137873-23-5
2-deoxy-D-arabino-hexono-1,4-lactone

Conditions

Conditions	Yield
With ethylenediaminetetraacetic acid In water for 48h; deoxyribose-5-phosphate aldolase (DERA), phosphate buffer, pH 7.3;	62%

: 583-50-6
D-erythrose

: 530-50-7
1,1-Diphenylhydrazine

: (2R,3S,E)-4-(2,2-diphenylhydrazono)butane-1,2,3-triol

Conditions

Conditions	Yield
In methanol at 20℃; for 0.75h;	57%
In methanol at 20℃; for 0.75h;	19%

: 540-63-6
ethane-1,2-dithiol

: 583-50-6
D-erythrose

: 145458-89-5
(1R,2R)-1-[1,3]Dithiolan-2-yl-propane-1,2,3-triol

Conditions

Conditions	Yield
With hydrogenchloride	55%

: 75-52-5
nitromethane

: 583-50-6
D-erythrose

A: 55065-39-9
1-Desoxy-1-nitro-D-arabino-pentitol

B: 130930-30-2
1-Deoxy-1-nitro-D-ribitol

Conditions

Conditions	Yield
With sodium methylate In methanol for 4h;	A 47% B 28%

...Expand

: 124-09-4
1,6-Hexanediamine

: 583-50-6
D-erythrose

: 1,6-bis(1-deoxy-D-erithritol-1-ylamino)hexane

Conditions

Conditions	Yield
With hydrogen; palladium on activated charcoal In methanol; water at 40℃; under 6750.68 Torr; for 24h;	47%

: 862470-02-8
7-amino-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-one

: 583-50-6
D-erythrose

: 908256-38-2
3-(2-trifluoromethylphenyl)-7-((2S,3R)-2,3,4-trihydroxybutylamino)-2H-isoquinolin-1-one

Conditions

Conditions	Yield
With sodium cyanoborohydride; acetic acid In tetrahydrofuran; methanol at 0 - 20℃; for 4h;	42%

: 312-84-5
D-Serine

: 583-50-6
D-erythrose

: 57-48-7
D-Fructose

Conditions

Conditions	Yield
With magnesium(II) chloride hexahydrate; flavin adenine dinucleotide (FAD)-containing flavoenzyme from the yeast Rhodotorula gracilis; thiamine pyrophosphate; oxygen In water at 25℃; for 8h; pH=7; Enzymatic reaction;	40%

: 583-50-6
D-erythrose

A: 533-50-6, 35007-64-8, 40031-31-0, 496-55-9
D-erythrulose

B: 95-43-2
D-threose

Conditions

Conditions	Yield
With zeolite H-USY In water at 120℃; for 3h; Catalytic behavior; Reagent/catalyst; Solvent; Temperature; Time; Concentration;	A 39% B 2%

: 583-50-6
D-erythrose

: 64-18-6
formic acid

Conditions

Conditions	Yield
With phosphovanadomolybdic acid; oxygen In water at 180℃; under 15001.5 Torr; for 3h;	38%

: 583-50-6
D-erythrose

A: 20246-26-8
D-threonic acid

B: 488-16-4
D-erythronic acid

Conditions

Conditions	Yield
With sodium anthraquinone-2-sulfonate; calcium chloride In sodium hydroxide at 50℃; Product distribution; further solvent, without catalyst; further D-aldoses;	A 34% B 29%
With sodium anthraquinone-2-sulfonate; calcium chloride In sodium hydroxide at 50℃;	A 34% B 29%

: 96-50-4
2-thiazolylamine

: 583-50-6
D-erythrose

: C10H14N4O3S2

Conditions

Conditions	Yield
In aq. buffer for 24h; pH=7;	32%

: 214044-53-8
C60H58N14O18S5

: 583-50-6
D-erythrose

C65H66N14O21S5: 1064084-29-2
C65H66N14O21S5

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 20℃; for 24h;	20%

: 67-56-1
methanol

: 74-93-1
methylthiol

: 583-50-6
D-erythrose

: 52703-96-5
methyl 2-hydroxy-4-(methylthio)butanoate

Conditions

Conditions	Yield
With potassium carbonate at 100℃; for 4h; Temperature;	20%

...Expand

: 113-24-6
sodium pyruvate

: 583-50-6
D-erythrose

: Sodium; (4S,5S,6R)-4,5,6,7-tetrahydroxy-2-oxo-heptanoate

Conditions

Conditions	Yield
With potassium dihydrogenphosphate; sodium azide In water for 96h; 2-keto-3-deoxy-6-phosphogluconate aldolase from Escherichia coli;	18.2%

: 583-50-6
D-erythrose

A: 67-47-0
5-hydroxymethyl-2-furfuraldehyde

B: 99-50-3
3,4-Dihydroxybenzoic acid

C: 1197-09-7
1-(3,4-dihydroxyphenyl)ethan-1-one

D: 55087-82-6
1-[5-(hydroxymethyl)furan-2-yl]ethan-1-one

E: 139-85-5
3,4-dihydroxybenzaldehyde

F: 488-17-5
3-methylbenzene-1,2-diol

Conditions

Conditions	Yield
With acetate buffer for 45h; Product distribution; Heating;	A 0.04% B 0.03% C 0.01% D 0.15% E 0.01% F 0.03%

...Expand

: 75-52-5
nitromethane

: 124-41-4
sodium methylate

: 583-50-6
D-erythrose

: 50-69-1
D-ribose

Conditions

Conditions	Yield
With methanol Eintragen einer wss.Loesung des Reaktionsprodukts in wss.Schwefelsaeure bei -20grad;

...Expand

: 75-52-5
nitromethane

: 583-50-6
D-erythrose

: 29810-07-9, 68107-77-7
1-nitro-D-erythro-pentene-(1)-triol-(3.4.5)-triacetate

Conditions

Conditions	Yield
With sodium methylate Behandlung mit Eisessig und mit Acetanhydrid + H2SO4 und folgendes Kochen mit NaHCO3 in Benzol;

: 583-50-6
D-erythrose

: 488-16-4
D-erythronic acid

Conditions

Conditions	Yield
With perchloric acid; sodium perchlorate; chromium (VI) Kinetics; Mechanism; ΔH=40 +/-3 kJ/mol, ΔS= -119 +/-10 J/deg.mol k2=14.9 1/mol.sec;
With water; bromine
With sodium hydroxide; osmium(VIII) oxide In water at 14.85℃; Rate constant; Thermodynamic data; ΔH, ΔS at 303 K;
With gold(III) chloride In water at 24.85℃; pH=3.72; Activation energy; Kinetics; Further Variations:; Reagents; pH-values;

: 583-50-6
D-erythrose

: 2319-57-5, 2418-52-2, 6968-16-7, 7493-90-5, 7541-59-5
1,2,3,4-butanetetrol

Conditions

Conditions	Yield
With sodium amalgam

D-Erythrose Specification

The CAS register number of D-Erythrose is 583-50-6. It also can be called as Butanal,2,3,4-trihydroxy-, (2R,3R)- and the IUPAC name about this chemical is (2S,3S)-2,3,4-trihydroxybutanal. The molecular formula about this chemical is C₄H₈O₄ and the molecular weight is 120.1. It belongs to the following product categories which include Carbohydrate Synthesis; Carbohydrates; Carbohydrates A to; Carbohydrates D-FBiochemicals and Reagents; Monosaccharides; MonosaccharideSpecialty Synthesis and so on.

Physical properties about D-Erythrose are: (1)ACD/LogP: -1.69; (2)ACD/LogD (pH 5.5): -1.69; (3)ACD/LogD (pH 7.4): -1.69; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 2.87; (7)ACD/KOC (pH 7.4): 2.87; (8)#H bond acceptors: 4; (9)#H bond donors: 3; (10)#Freely Rotating Bonds: 6; (11)Polar Surface Area: 44.76Å²; (12)Index of Refraction: 1.505; (13)Molar Refractivity: 25.28 cm³; (14)Molar Volume: 85.1 cm³; (15)Polarizability: 10.02x10^-24cm³; (16)Surface Tension: 68.6 dyne/cm; (17)Enthalpy of Vaporization: 64.01 kJ/mol; (18)Boiling Point: 311.1 °C at 760 mmHg; (19)Vapour Pressure: 5.12E-05 mmHg at 25°C.

When you are using this chemical, please be cautious about it as the following:
This chemical is irritating to eyes, respiratory system and skin. When you are using it, please avoid contact with skin and eyes and wear suitable protective clothing. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
(1)SMILES: O=C[C@H](O)[C@H](O)CO
(2)InChI: InChI=1/C4H8O4/c5-1-3(7)4(8)2-6/h1,3-4,6-8H,2H2/t3-,4+/m0/s1
(3)InChIKey: YTBSYETUWUMLBZ-IUYQGCFVBI
(4)Std. InChI: InChI=1S/C4H8O4/c5-1-3(7)4(8)2-6/h1,3-4,6-8H,2H2/t3-,4+/m0/s1
(5)Std. InChIKey: YTBSYETUWUMLBZ-IUYQGCFVSA-N

Product Name

D-(-)-ERYTHROSE

Synthetic route

D-Erythrose Specification

Related Products

Hot Products