tert-butyl (3-hydroxypropyl)methylcarbamate
propan-1-ol-3-amine
Conditions | Yield |
---|---|
With hydrogenchloride for 2h; | 99% |
Conditions | Yield |
---|---|
With ammonium hydroxide; hydrogen; silver nitrate In methanol at 45 - 75℃; under 1500.15 Torr; Temperature; High pressure; Inert atmosphere; Autoclave; | 98% |
With hydrogen; nickel In isopropyl alcohol at 60℃; under 3102.9 Torr; 20-24 h; | 88% |
With ammonium hydroxide; hydrogen at 80℃; under 60006 Torr; for 6h; Sealed tube; | 80% |
Conditions | Yield |
---|---|
With ammonium formate; palladium on activated charcoal In methanol for 0.166667h; Heating; | 95% |
Conditions | Yield |
---|---|
With palladium on activated charcoal; hydrogen In dichloromethane; water at 40℃; under 3375.34 Torr; for 4h; Temperature; Pressure; Solvent; Autoclave; | 93.8% |
Conditions | Yield |
---|---|
With sulfuric acid; hydrogen In water at 79.84℃; under 60006 Torr; | 90% |
With ruthenium trichloride; sulfuric acid; hydrogen In water at 95℃; for 10h; pH=4; Temperature; Reagent/catalyst; Autoclave; | 88.09% |
With tetrahydrofuran; lithium aluminium tetrahydride |
3-trimethylsiloxy-1-phenylpropyl isocyanide
propan-1-ol-3-amine
Conditions | Yield |
---|---|
With hydrogenchloride In methanol at 24℃; for 12h; | 65% |
Conditions | Yield |
---|---|
55% |
Conditions | Yield |
---|---|
With water; nickel at 140℃; under 51485.6 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether |
Conditions | Yield |
---|---|
With ammonia; nickel at 110 - 115℃; Hydrogenation.unter Druck; |
3-nitropropan-1-ol
propan-1-ol-3-amine
Conditions | Yield |
---|---|
With hydrogenchloride; tin |
3-amino-2-propanol
propan-1-ol-3-amine
Conditions | Yield |
---|---|
With methanol; ammonia at 110 - 140℃; |
Conditions | Yield |
---|---|
With nickel kieselguhr at 60 - 70℃; Hydrogenation.unter Druck; |
Conditions | Yield |
---|---|
With perchloric acid at 25℃; Rate constant; Thermodynamic data; E(a); |
propylamine
A
3-aminopropanal
B
oxalic acid
C
propionic acid
D
glycine
E
propan-1-ol-3-amine
F
3-amino propanoic acid
Conditions | Yield |
---|---|
With argon arc plasma; water at 30℃; Product distribution; cathode: tungsten rod; anode: copper nozzle; 40 A; 10 V; pH= 3.0; variation of concentration of substrate and time; |
propylamine
A
2-Amino-1-propanol
B
(RS)-isoserine
C
glycine
D
propan-1-ol-3-amine
E
3-amino propanoic acid
Conditions | Yield |
---|---|
In water at 10 - 20℃; Product distribution; pH=2.7 and pH=12.0, various reaction times, contact glow discharge electrolysis; |
propylamine
A
(RS)-isoserine
B
glycine
C
propan-1-ol-3-amine
D
3-amino propanoic acid
Conditions | Yield |
---|---|
In water at 10 - 20℃; contact glow discharge electrolysis, pH=2.7; Yield given. Further byproducts given; |
propylamine
A
3-aminopropanal
B
glycine
C
propan-1-ol-3-amine
D
3-amino propanoic acid
Conditions | Yield |
---|---|
town gas-oxigen flame In water at 40 - 50℃; for 0.25h; | A 7.1 % Chromat. B n/a C 8.9 % Chromat. D n/a |
3-chloropropan-1-amine
A
azetidine
B
3-(3-aminopropylamino)propan-1-ol
C
N-γ-aminopropyltrimethyleneimine
D
N1-(3-Azetidin-1-yl-propyl)-propane-1,3-diamine
E
1-amino-2-propene
F
propan-1-ol-3-amine
Conditions | Yield |
---|---|
With sodium hydroxide In water at 80℃; Product distribution; | A n/a B 6 % Chromat. C 50 % Chromat. D 25 % Chromat. E n/a F 15 % Chromat. |
3-hydroxypropan-1-aminium
C14H13NO
A
1-methyl-4-(phenylacetyl)pyridinium cation
B
propan-1-ol-3-amine
Conditions | Yield |
---|---|
In water at 25℃; Equilibrium constant; Rate constant; |
N-3-phenoxypropylacetamide
A
acetic acid
B
propan-1-ol-3-amine
C
3-phenoxypropanamine
D
phenol
Conditions | Yield |
---|---|
With hydrogenchloride In 1,4-dioxane at 94.5℃; Product distribution; Mechanism; Kinetics; velocity const; different HCl conc.;var. temp.; |
N-3-phenoxypropylpropionamide
A
propionic acid
B
propan-1-ol-3-amine
C
3-phenoxypropanamine
D
phenol
Conditions | Yield |
---|---|
With hydrogenchloride In 1,4-dioxane at 94.5℃; Product distribution; Mechanism; Kinetics; velocity const; different HCl conc.; var. temp.; |
[1,3]-dioxolan-2-one
propan-1-ol-3-amine
(3-hydroxy-propyl)-carbamic acid-(2-hydroxy-ethyl ester)
Conditions | Yield |
---|---|
1) 50-55 deg C, 1 h; 2) r.t., overnight; | 100% |
Conditions | Yield |
---|---|
In toluene at 125℃; for 6.5h; Inert atmosphere; | 100% |
With triethylamine In toluene at 125℃; for 3h; Inert atmosphere; Dean-Stark; | 99% |
With triethylamine In toluene at 130℃; for 3h; | 95% |
propan-1-ol-3-amine
formic acid ethyl ester
3-(N-formylamino)propan-1-ol
Conditions | Yield |
---|---|
100% | |
Reflux; | 100% |
at 50℃; for 2.25h; Cooling with ice; | 95% |
phosphonic acid diethyl ester
propan-1-ol-3-amine
(3-hydroxy-propyl)-phosphoramidic acid diethyl ester
Conditions | Yield |
---|---|
With potassium carbonate; potassium hydrogencarbonate; tetrabutylammomium bromide In tetrachloromethane; dichloromethane at 15 - 20℃; for 2h; | 100% |
With triethylamine In tetrachloromethane; benzene | |
With sodium hypochlorite In water at 0℃; Temperature; | 8.6 g |
p-toluenesulfonyl chloride
propan-1-ol-3-amine
3-[N-(4-methylphenylsulfonyl)amino]propan-1-ol
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 1h; Inert atmosphere; | 100% |
With triethylamine In dichloromethane at 0℃; for 17h; | 99% |
With triethylamine In chloroform at 0 - 20℃; for 18h; Inert atmosphere; | 99% |
pyridine-2-carbaldehyde
propan-1-ol-3-amine
tetrahydro-2-(2-pyridinyl)-2H-1,3-oxazine
Conditions | Yield |
---|---|
In ethanol for 2h; Product distribution; Ambient temperature; other aminoalcohols, other pyridinecarbaldehydes; | 100% |
In ethanol for 2h; Ambient temperature; | 100% |
propan-1-ol-3-amine
N-acetyl-1,3-oxazol-2-one
N-(3-hydroxypropyl)acetamide
Conditions | Yield |
---|---|
In tetrahydrofuran for 1h; Ambient temperature; | 100% |
propan-1-ol-3-amine
4-bromobutanenitrile
4-(3-Hydroxy-propylamino)-butyronitrile
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile for 20h; Heating; | 100% |
With potassium carbonate; sodium iodide In acetonitrile for 20h; Alkylation; Heating; | 6.70 g |
tert-butyldimethylsilyl chloride
propan-1-ol-3-amine
3-(tertbutyldimethylsiloxyl)propylamine
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; | 100% |
With 1H-imidazole In dichloromethane at 20℃; | 99% |
With triethylamine In dichloromethane at 20℃; for 12h; | 97% |
propan-1-ol-3-amine
4-Benzenesulfonyl-N-(3-hydroxy-propyl)-butyramide
Conditions | Yield |
---|---|
In dichloromethane at 0℃; | 100% |
propan-1-ol-3-amine
5-Benzenesulfonyl-pentanoic acid (3-hydroxy-propyl)-amide
Conditions | Yield |
---|---|
In dichloromethane at 0℃; | 100% |
propan-1-ol-3-amine
6-Benzenesulfonyl-hexanoic acid (3-hydroxy-propyl)-amide
Conditions | Yield |
---|---|
In dichloromethane at 0℃; | 100% |
propan-1-ol-3-amine
7-Benzenesulfonyl-heptanoic acid (3-hydroxy-propyl)-amide
Conditions | Yield |
---|---|
In dichloromethane at 0℃; | 100% |
1,8-Naphthalic anhydride
propan-1-ol-3-amine
N-(3-hydroxypropyl)-1,8-naphthalimide
Conditions | Yield |
---|---|
100% | |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In N,N-dimethyl-formamide at 85℃; for 4h; Inert atmosphere; | 98% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In N,N-dimethyl-formamide at 85℃; for 4h; | 95% |
formaldehyd
propan-1-ol-3-amine
3-[3,5-bis(3-hydroxypropyl)[1,3,5]triazinan-1-yl]propan-1-ol
Conditions | Yield |
---|---|
In methanol at 20℃; for 16h; | 100% |
In acetonitrile at 20℃; | 92% |
In ethanol Cyclization; |
4'-nitrobenzo-15-crown-5
propan-1-ol-3-amine
Conditions | Yield |
---|---|
In ethanol at 100℃; for 100h; Ring cleavage; | 100% |
C23H28N4O2
propan-1-ol-3-amine
Conditions | Yield |
---|---|
at 20℃; for 1h; Substitution; | 100% |
3,6-dimethylthio-1,2,4,5-tetrazine
propan-1-ol-3-amine
3-((6-methylthio-1,2,4,5-tetrazin-3-yl)amino)propan-1-ol
Conditions | Yield |
---|---|
With 3 Angstroem MS In methanol at 25℃; for 18h; | 100% |
3,4,5-trimethoxy-benzaldehyde
propan-1-ol-3-amine
2-(3,4,5-trimethoxy)phenyltetrahydro-(2H)-1,3-oxazine
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene Heating; | 100% |
3,4-dimethoxy-benzaldehyde
propan-1-ol-3-amine
2-(3,4-dimethoxy)phenyltetrahydro-(2H)-1,3-oxazine
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene Heating; | 100% |
N-tert-butyloxycarbonylpiperidin-4-one
propan-1-ol-3-amine
tert-butyl 4-[(3-hydroxypropyl)amino]piperidine-1-carboxylate
Conditions | Yield |
---|---|
With hydrogen; palladium 10% on activated carbon In ethanol under 3361.55 Torr; for 1.5h; | 100% |
With hydrogen; palladium on activated charcoal In methanol at 20℃; under 760.051 Torr; for 24h; | 99% |
With sodium tris(acetoxy)borohydride In 1,2-dichloro-ethane for 2h; | |
Stage #1: N-tert-butyloxycarbonylpiperidin-4-one; propan-1-ol-3-amine With acetic acid In dichloromethane at 20 - 27℃; for 3h; Stage #2: With sodium tris(acetoxy)borohydride In dichloromethane at 20 - 27℃; Inert atmosphere; |
MF: C3H9NO
MW: 75.11
EINECS: 205-864-4
mp: 10-12 °C(lit.)
bp: 184-187 °C(lit.)
density: 0.987 g/mL at 20 °C(lit.)
vapor density: 2.59 (vs air)
vapor pressure: 2.1 mm Hg ( 20 °C)
refractive index: n20/D 1.4598(lit.)
Fp: 175 °F
Water Solubility: miscible
Sensitive: Hygroscopic
BRN: 741855
CAS DataBase Reference: 156-87-6(CAS DataBase Reference)
NIST Chemistry Reference: 156-87-6(NIST)
The structure of 3-PROPANOLAMINE is:
1. | skn-rbt 10 mg/24H open SEV | AIHAAP American Industrial Hygiene Association Journal. 23 (1962),95. | ||
2. | eye-rbt 250 µg/24H SEV | 85JCAE Prehled Prumyslove Toxikologie; Organicke Latky Marhold, J.,Prague, Czechoslovakia.: Avicenum,1986,683. | ||
3. | orl-rat LDLo:2830 mg/kg | AIHAAP American Industrial Hygiene Association Journal. 23 (1962),95. | ||
4. | skn-rbt LD50:1250 mg/kg | AIHAAP American Industrial Hygiene Association Journal. 23 (1962),95. |
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View