Conditions | Yield |
---|---|
With formic acid | |
With ethanol; water; sodium acetate Hydrieren des Reaktionsgemisches in Gegenwart von Raney-Nickel bei 65grad/70 at; | |
With formic acid |
2-chloro-1-dimethylaminopropane
2-(dimethylamino)propan-1-ol
Conditions | Yield |
---|---|
With silver(l) oxide |
ethyl 2-(N,N-dimethylamino)-propionate
2-(dimethylamino)propan-1-ol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether |
Conditions | Yield |
---|---|
(i) H2O, (ii) EtOH, HCl, (iii) LiAlH4, Et2O; Multistep reaction; |
dimethyl amine
Ethyl 2-bromopropionate
2-(dimethylamino)propan-1-ol
Conditions | Yield |
---|---|
(i) Et2O, (ii) LiAlH4; Multistep reaction; |
A
2-(dimethylamino)propan-1-ol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether at 23℃; |
2-(dimethylamino)propan-1-ol
Conditions | Yield |
---|---|
With ethanol; sodium |
2-chloro-1-dimethylaminopropane
2-(dimethylamino)propan-1-ol
sodium thiocyanide
copper(II) acetate monohydrate
2-(dimethylamino)propan-1-ol
[Cu((CH3)3NCHCH2O)(NCS)]2
Conditions | Yield |
---|---|
In methanol MeOH soln. of NaNCS was added to MeOH soln. of Cu(OAc)2*H2O and ligand, allowed to stand at 25°C for several ds; filtered, dried in vacuo; elem. anal.; | 90% |
5-(2-Chloro-phenyl)-2-methylsulfonyl-pyrimidine-4-carboxylic acid (3,5-bis-trifluoromethyl-benzyl)-methyl-amide
2-(dimethylamino)propan-1-ol
5-(2-chloro-phenyl)-2-(3-dimethylamino-propoxy)-pyrimidine-4-carboxylic acid (3,5-bis-trifluoromethyl-benzyl)-methyl-amide
Conditions | Yield |
---|---|
With caesium carbonate In acetonitrile for 16h; | 77% |
2-(dimethylamino)propan-1-ol
N,N-dimethyl acetamide
Conditions | Yield |
---|---|
With potassium hydroxide; air In diethyl ether at 20℃; for 90h; | 73% |
diphenylacetic acid chloride
2-(dimethylamino)propan-1-ol
Conditions | Yield |
---|---|
With benzene |
3,3-diphenylpropanoyl chloride
2-(dimethylamino)propan-1-ol
N,N-dicyclohexylcarbamoyl chloride
2-(dimethylamino)propan-1-ol
Conditions | Yield |
---|---|
With toluene |
2-(dimethylamino)propan-1-ol
acetic anhydride
(β-acetoxy-isopropyl)-trimethyl-ammonium; iodide
Conditions | Yield |
---|---|
Umsetzung des Reaktionsprodukts mit Methyljodid; |
2-(dimethylamino)propan-1-ol
succinoyl dichloride
succinic acid bis-(2-dimethylamino-propyl ester)
Conditions | Yield |
---|---|
With hydrogenchloride; chloroform |
2-(dimethylamino)propan-1-ol
acryloyl chloride
acrylic acid-(2-dimethylamino-propyl ester)
Conditions | Yield |
---|---|
With benzene |
2-(dimethylamino)propan-1-ol
methyl iodide
(β-hydroxy-isopropyl)-trimethyl-ammonium; hydroxide
Conditions | Yield |
---|---|
With ethanol und nachfolgendem Behandeln des entstandenen Jodids mit Silberoxyd; |
2-(dimethylamino)propan-1-ol
methyl iodide
(β-hydroxy-isopropyl)-trimethyl-ammonium; iodide
Conditions | Yield |
---|---|
With ethanol |
2-(dimethylamino)propan-1-ol
2-(dimethyl-amino)-1-methylethylchloride hydrochloride
Conditions | Yield |
---|---|
With thionyl chloride; chloroform | |
With thionyl chloride; benzene zuletzt bei Siedepemperatur; | |
With thionyl chloride In chloroform at -60 - 60℃; |
2-(dimethylamino)propan-1-ol
2-chloro-1-dimethylaminopropane
Conditions | Yield |
---|---|
With thionyl chloride; benzene |
styrene oxide
2-(dimethylamino)propan-1-ol
2-(2-Dimethylamino-propyloxy)-1-phenyl-ethanol-(1)
Conditions | Yield |
---|---|
(i) Na, (ii) /BRN= 108582/; Multistep reaction; |
methyl benzilate
2-(dimethylamino)propan-1-ol
benzilic acid-(2-dimethylamino-propyl ester)
Conditions | Yield |
---|---|
With sodium In benzene |
ethyl 2-cyclohexyl-2-hydroxy-2-phenylacetate
2-(dimethylamino)propan-1-ol
Cyclohexyl-phenyl-glykolsaeure-<2-dimethylamino-propylester>
Conditions | Yield |
---|---|
With sodium In benzene |
Conditions | Yield |
---|---|
(i) HCl, CHCl3, (ii) /BRN= 505934/, EtOH; Multistep reaction; |
Conditions | Yield |
---|---|
(i) HCl, CHCl3, (ii) /BRN= 505934/, EtOH; Multistep reaction; |
2-(dimethylamino)propan-1-ol
allyl bromide
2-Dimethylamino-1-allyloxy-propan
Conditions | Yield |
---|---|
(i) NaH, toluene, (ii) /BRN= 605308/; Multistep reaction; |
2-(dimethylamino)propan-1-ol
ethyl vinyl ether
Dimethyl-(1-methyl-2-vinyloxy-ethyl)-amine
Conditions | Yield |
---|---|
With mercury(II) diacetate Heating; |
2-(dimethylamino)propan-1-ol
4-chlorobenzoyl chloride
Conditions | Yield |
---|---|
With pyridine at 23℃; |
2-(dimethylamino)propan-1-ol
N,N-Dimethylcarbamoyl chloride
Conditions | Yield |
---|---|
With sodium hydride In toluene for 24h; Ambient temperature; Yield given; |
The 1-Propanol,2-(dimethylamino)-, with the CAS registry number 15521-18-3, is also known as N,N-Dimethyl-2-aminopropan-1-ol. Its EINECS number is 239-558-7. This chemical's molecular formula is C5H13NO and molecular weight is 103.16. What's more, its IUPAC name is 2-(dimethylamino)propan-1-ol.
Physical properties of 1-Propanol,2-(dimethylamino)- are: (1)ACD/LogP: 0.02; (2)# of Rule of 5 Violations: 0; (3)#H bond acceptors: 2; (4)#H bond donors: 1; (5)#Freely Rotating Bonds: 3; (6)Polar Surface Area: 23.47 Å2; (7)Index of Refraction: 1.436; (8)Molar Refractivity: 30.42 cm3; (9)Molar Volume: 116.2 cm3; (10)Polarizability: 12.06×10-24cm3; (11)Surface Tension: 29.5 dyne/cm; (12)Density: 0.887 g/cm3; (13)Flash Point: 32.1 °C; (14)Enthalpy of Vaporization: 43.26 kJ/mol; (15)Boiling Point: 133.8 °C at 760 mmHg; (16)Vapour Pressure: 3.62 mmHg at 25°C.
Uses of 1-Propanol,2-(dimethylamino)-: it can be used to produce N,N-dimethyl-acetamide at the temperature of 20 °C. It will need reagents KOH, air and solvent diethyl ether with the reaction time of 90 hours. The yield is about 73%.
You can still convert the following datas into molecular structure:
(1)Canonical SMILES: CC(CO)N(C)C
(2)InChI: InChI=1S/C5H13NO/c1-5(4-7)6(2)3/h5,7H,4H2,1-3H3
(3)InChIKey: PBKGYWLWIJLDGZ-UHFFFAOYSA-N
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