2-acetoxypropionic acid
3-acetoxypropionic acid
A
LACTIC ACID
B
3-hydroxypropionic acid
Conditions | Yield |
---|---|
With water; Amberlite IR 120 at 80℃; for 16h; Product distribution / selectivity; | A 100% B 100% |
With water; hydrogenchloride at 100℃; for 16h; Product distribution / selectivity; | |
With water; toluene-4-sulfonic acid at 100℃; for 16h; Product distribution / selectivity; |
3-hydroxypropionic acid
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In methanol under 2888.19 Torr; for 0.666667h; | 100% |
With palladium 10% on activated carbon; hydrogen In methanol under 2888.19 Torr; for 0.666667h; Baeyer-Villiger Ketone Oxidation; | 100% |
Conditions | Yield |
---|---|
With sodium hydroxide In water; hexan-1-ol at 80℃; for 2h; Solvent; Temperature; Reagent/catalyst; | 99% |
With rhodium on carbon; water; hydrogen iodide; hydrogen at 99.84℃; under 20686.5 Torr; for 1h; Autoclave; | 69.4% |
With water; silver(l) oxide | |
With water; silver(l) oxide man behandelt das Filtrat mit Schwefelwasserstoff, filtriert ab, neutralisiert das Filtrat mit Soda, verdampft und zieht das hydracrylsaure Natrium durch Alkohol aus und krystallisiert beim Erkalten aus; |
Conditions | Yield |
---|---|
Stage #1: 3-Hydroxypropionitrile With sodium hydroxide In water for 8h; Reflux; Saturated solution; Stage #2: With hydrogenchloride In water | 92.1% |
With hydrogenchloride; water for 4h; Reagent/catalyst; | 89% |
With sodium hydroxide for 12h; Ambient temperature; | 75% |
Conditions | Yield |
---|---|
With sodium hydroxide In methanol | 77% |
With barium dihydroxide; water | |
With water In 1,4-dioxane at 25℃; Kinetics; Further Variations:; Temperatures; Solvents; |
Conditions | Yield |
---|---|
With ammonia; Ti-0720 (Engelhard) catalyst In water at 200 - 250℃; for 37h; Product distribution / selectivity; | A n/a B 75% C n/a |
titanium catalyst In water at 180℃; for 37h; Product distribution / selectivity; | A 1.5% B 65% C n/a |
titanium catalyst In water at 180℃; for 37h; Product distribution / selectivity; | A 1.5% B 65% C n/a |
Conditions | Yield |
---|---|
With oxygen; sodium hydroxide In water at 50℃; Reagent/catalyst; Sonication; | A 60.1% B 21.3% |
With water; oxygen; sodium hydroxide at 50℃; under 2250.23 Torr; for 24h; | A 51.1% B 28.4% |
With oxygen; sodium hydroxide In water at 50℃; under 2250.23 Torr; for 12h; |
levulinic acid
A
formic acid
B
succinic acid
C
trifluoroacetic acid-methyl ester
D
acetic acid
E
3-hydroxypropionic acid
Conditions | Yield |
---|---|
With dihydrogen peroxide; trifluoroacetic acid In water at -78 - 90℃; for 1.66667h; | A 45% B 60% C 45% D 43% E 9% |
levulinic acid
trifluoroacetic acid
A
formic acid
B
succinic acid
C
trifluoroacetic acid-methyl ester
D
acetic acid
E
3-hydroxypropionic acid
Conditions | Yield |
---|---|
With dihydrogen peroxide In water at 90℃; for 1h; | A 45 %Spectr. B 60% C 45 %Spectr. D 43 %Spectr. E 9 %Spectr. |
Conditions | Yield |
---|---|
With dihydrogen peroxide In water at 90℃; under 7600.51 Torr; for 12h; Reagent/catalyst; Temperature; Solvent; Pressure; Inert atmosphere; | 58% |
Conditions | Yield |
---|---|
With water at 230℃; for 2h; sealed tube; | 56% |
With water at 200℃; reaction order of hydration, kinetic curves; other temperatures; | |
With sulfuric acid at 101.5℃; Kinetics; var. ratio of reactants, var. temperature; | |
With 4-methoxy-phenol In water at 80℃; Temperature; Flow reactor; |
Conditions | Yield |
---|---|
With dihydrogen peroxide; potassium hydroxide In water at 0 - 115℃; for 1h; Baeyer-Villiger Ketone Oxidation; | 45% |
allyl alcohol
A
glyceric acid
B
acrylic acid
C
3-hydroxypropionic acid
Conditions | Yield |
---|---|
With oxygen; sodium hydroxide In water at 50℃; Reagent/catalyst; Sonication; | A 6.9% B 30.1% C 7.2% |
Conditions | Yield |
---|---|
With cerium(IV) oxide Reagent/catalyst; | A 19% B 23.2% |
With nano gold salt supported on cerium oxide | A 10.7% B 9.4% |
propargyl alcohol
A
ethene
B
hydroxy-2-propanone
C
acrylic acid
D
3-hydroxypropionic acid
Conditions | Yield |
---|---|
With water; ruthenium tetrasulphthalocyanine at 80℃; for 24h; Product distribution; Further Variations:; Catalysts; anti-Markovnikov hydration; | A n/a B 10% C 22% D 10% |
Conditions | Yield |
---|---|
With nano gold salt | 21.1% |
With iron(III) oxide | 14.4% |
Conditions | Yield |
---|---|
at 50 - 60℃; Behandeln des erhaltenen Nitrils mit rauchender Salzsaeure; |
Conditions | Yield |
---|---|
With water quantitativer Verlauf der Bildung; | |
With sodium hydroxide quantitativer Verlauf der Bildung; |
Conditions | Yield |
---|---|
With Fehling's solution at 240℃; | |
at 240℃; bei loegeren Erhitzen mit Fehlingscher Loesung; | |
at 240℃; bei 200-stuendigem Erhitzen mit Fehlingscher Loesung; |
Conditions | Yield |
---|---|
With water | |
With calcium hydroxide |
1-hydroxy-5-methyl-hept-4-en-3-one
chloroform
A
butanone
B
3-hydroxypropionic acid
Conditions | Yield |
---|---|
bei der Ozonspaltung; 7-hydroxy-3-methyl-hepten-(3)-one-(5); |
peracetic acid
diethyl 1,3-acetonedicarboxylate
A
oxalic acid
B
3-hydroxypropionic acid
potassium cyanide
2-chloro-ethanol
A
LACTIC ACID
B
3-hydroxypropionic acid
Conditions | Yield |
---|---|
Verseifung des gebildeten Nitrils mit Natronlauge; | |
Verseifung des gebildeten Nitrils mit rauchender Salzsaeure; |
Conditions | Yield |
---|---|
With sulfuric acid In water at 25℃; Rate constant; | |
With sulfuric acid at 25 - 85℃; Kinetics; Mechanism; Thermodynamic data; ΔH(excit.), -ΔS(excit.); |
3,12-bis(3'-bromo-1'-oxopropyl)-3,12-diaza-6,9-diazoniadispiro<5.2.5.2>hexadecane dichloride
A
3-Bromopropionic acid
B
chloropropionic acid
C
3,12-bis(3'-chloro-1'-oxopropyl)-3,12-diaza-6,9-diazoniadispiro<5.2.5.2>hexadecane dibromide
D
3,12-Bisacrylyl-3,12-diaza-6,9-diazoniadispiro<5,2,5,2>hexadecane dichloride
E
3,12-bis(3'-hydroxy-1'-oxopropyl)-3,12-diaza-6,9-diazoniadispiro<5.2.5.2>hexadecane dichloride
F
3-hydroxypropionic acid
Conditions | Yield |
---|---|
In water at 70℃; for 5h; Product distribution; Kinetics; Rate constant; various time; other temperature; |
propionic acid
A
formic acid
B
glycolic Acid
C
LACTIC ACID
D
malonic acid
E
acetic acid
F
3-hydroxypropionic acid
Conditions | Yield |
---|---|
With dihydrogen peroxide In water at 20℃; Product distribution; Mechanism; Irradiation; effect of H2O2/proponic acid ratio, iraadiation time; |
propionic acid
A
LACTIC ACID
B
malonic acid
C
acetic acid
D
3-hydroxypropionic acid
Conditions | Yield |
---|---|
With dihydrogen peroxide In water at 20℃; Irradiation; Further byproducts given; |
A
3-benzenesulfonylamino-propionic acid
B
benzenesulfonic acid
C
3-hydroxypropionic acid
Conditions | Yield |
---|---|
With sulfuric acid In water at 25℃; Rate constant; |
acrylic acid
A
LACTIC ACID
B
glyceric acid
C
propionic acid
D
3-hydroxypropionic acid
Conditions | Yield |
---|---|
With dihydrogen peroxide In water at 30℃; Product distribution; Irradiation; 40/90 mA, 750 V, photooxidation by glow discharge electrolysis in various cells, with various reaction times and currents, at various temperatures with or without irradiation; | |
With dihydrogen peroxide In water Product distribution; Quantum yield; Irradiation; var. amount of absorbed energy; |
Conditions | Yield |
---|---|
titanium catalyst 16-30 mesh at 180 - 190℃; for 45h; Product distribution / selectivity; | 100% |
With 4-methoxy-phenol; silica gel at 250℃; Gas phase; | 97% |
sulfuric acid at 160℃; Product distribution / selectivity; | 96.2% |
N-methyl-N-tert-butyldimethylsilyl-1,1,1-trifluoroacetamide
3-hydroxypropionic acid
C15H34O3Si2
Conditions | Yield |
---|---|
With tert-butyldimethylsilyl chloride In acetonitrile for 0.0833333h; Ambient temperature; other silylating agent; | 100% |
Conditions | Yield |
---|---|
With 4-methoxy-phenol; EM-1500 zeolite at 150℃; Product distribution / selectivity; Gas phase; | 97.4% |
With sulfuric acid; copper at 155 - 165℃; | |
With phosphoric acid; copper at 135 - 145℃; |
Conditions | Yield |
---|---|
With sodium hydroxide In water | 97% |
With sodium hydroxide elektrochemische Oxydation, am besten an einer Nickelanode; |
benzylamine
3-hydroxypropionic acid
3-hydroxy-N-(phenylmethyl)propanamide
Conditions | Yield |
---|---|
With 4-(2-(1,3-dioxa-3a1,8,10-triaza-2,3a,14b-triboradibenzo[fg,op]tetracen-2-yl)phenyl)benzo[c]pyrimido[4,5-e][1,2]azaborinin-6(5H)-ol In fluorobenzene at 85℃; for 8h; Molecular sieve; | 94% |
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 14h; | 93% |
tert-butyldimethylsilyl chloride
3-hydroxypropionic acid
3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]propanoic acid
Conditions | Yield |
---|---|
With 1H-imidazole In dichloromethane | 92% |
Conditions | Yield |
---|---|
In methanol at 60℃; for 20h; | 92% |
Conditions | Yield |
---|---|
With hydrogen In water at 100℃; under 37503.8 Torr; for 30h; Pressure; Reagent/catalyst; Autoclave; | A 10% B 85% |
N-δ-Boc-3-hydroxy-DL-ornithine tert-butyl ester
3-hydroxypropionic acid
5-tert-Butoxycarbonylamino-3-hydroxy-2-(3-hydroxy-propionylamino)-pentanoic acid tert-butyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 16h; | 82% |
H-Orn(Z)-OBzl
3-hydroxypropionic acid
(S)-5-Benzyloxycarbonylamino-2-(3-hydroxy-propionylamino)-pentanoic acid benzyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 16h; | 81% |
Conditions | Yield |
---|---|
With ruthenium-carbon composite; hydrogen In water at 119.84℃; under 7500.75 - 60006 Torr; for 2h; Catalytic behavior; Autoclave; Sealed tube; | A 18% B 79% |
Conditions | Yield |
---|---|
With pyridinium p-toluenesulfonate In N,N-dimethyl-formamide at 70℃; for 5h; | 75% |
3-hydroxypropionic acid
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In water; N,N-dimethyl-formamide at 20℃; for 15h; | 74.3% |
Conditions | Yield |
---|---|
With sodium at 50℃; | 72.1% |
With copper(II) sulfate | |
sulfuric acid at 20℃; for 1.5 - 22h; Product distribution / selectivity; | 75 - 95 %Chromat. |
3-hydroxypropionic acid
Conditions | Yield |
---|---|
With triethylamine; N-ethyl-N,N-diisopropylamine; HATU In tetrahydrofuran at 20℃; for 2h; Inert atmosphere; | 68% |
Conditions | Yield |
---|---|
With sulfuric acid at 78 - 80℃; under 760.051 Torr; for 10h; Time; | 67.24% |
With copper(II) sulfate | |
amberlyst-15 at 20℃; for 19h; Product distribution / selectivity; | 17 - 68 %Chromat. |
Nafion NR-50 at 20℃; for 21h; Product distribution / selectivity; | 71 %Chromat. |
Conditions | Yield |
---|---|
In tetrahydrofuran; N,N-dimethyl-formamide for 1h; | 61% |
4-amino-6,7-dimethoxy-2-piperazin-1-ylquinazoline
3-hydroxypropionic acid
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; ethyl cyanoglyoxylate-2-oxime In N,N-dimethyl-formamide at 20℃; | 61% |
Conditions | Yield |
---|---|
With hydrogen; molybdenum(IV) oxide In water at 150℃; under 78334.3 Torr; for 3h; Product distribution / selectivity; | 60% |
With hydrogen; molybdenum In ISOPAR K; water at 150℃; under 78334.3 Torr; for 3h; Product distribution / selectivity; | 57% |
With hydrogen In water at 100℃; under 78334.3 Torr; for 16h; Product distribution / selectivity; | 47% |
Molecular structure of Propanoic acid,3-hydroxy- (CAS NO.503-66-2) is:
Product Name: Propanoic acid,3-hydroxy-
CAS Registry Number: 503-66-2
IUPAC Name: 3-Hydroxypropanoic acid
Molecular Weight: 90.07794 [g/mol]
Molecular Formula: C3H6O3
XLogP3-AA: -1
H-Bond Donor: 2
H-Bond Acceptor: 3
EINECS: 207-974-8
Surface Tension: 53.7 dyne/cm
Density: 1.283 g/cm3
Flash Point: 137.2 °C
Enthalpy of Vaporization: 60.18 kJ/mol
Boiling Point: 279.7 °C at 760 mmHg
Vapour Pressure: 0.000476 mmHg at 25°C
Product Categories: Aliphatics;Carboxylic Acids;omega-Functional Alkanols, Carboxylic Acids, Amines & Halides;omega-Hydroxycarboxylic Acids;Carboxylic Acids
Safty information about Propanoic acid,3-hydroxy- (CAS NO.503-66-2) is:
Hazard Codes: Xi
Risk Statements: 36/37/38
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 26-36/37/39
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection.
Propanoic acid,3-hydroxy- , its cas register number is 503-66-2. It also can be called 3-Hydroxypropanoic acid ; Ethylene lactic acid ; Glyceric acid, 2-deoxy- ; Hydracrylic acid ; beta-Hydroxypropionic acid ; beta-Lactic acid .
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