5-tosyloxy-3-oxapentanol
diethylamine
2-[2-(diethylamino)ethoxy] ethanol
Conditions | Yield |
---|---|
With potassium carbonate In 1,4-dioxane at 70℃; | 42% |
Conditions | Yield |
---|---|
at 100℃; | |
at 100℃; |
2-(2-chloroethoxy)ethyl ethanoate
diethylamine
2-[2-(diethylamino)ethoxy] ethanol
Conditions | Yield |
---|---|
With ethanol at 125℃; |
Methyl-N,N-diethyldiglycollamat
2-[2-(diethylamino)ethoxy] ethanol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride |
2-(Diethylamino)ethanol
2-chloro-ethanol
2-[2-(diethylamino)ethoxy] ethanol
Conditions | Yield |
---|---|
With sodium |
Conditions | Yield |
---|---|
With benzene |
Dorex
A
α-Ethyl-α-phenylbutyric acid
B
2-[2-(diethylamino)ethoxy] ethanol
Conditions | Yield |
---|---|
With sodium hydroxide at 100℃; for 3h; |
Conditions | Yield |
---|---|
With NaBH3CN In methanol; water | |
With NaBH3CN In methanol; water |
2-Heptadecafluorooctyl-oxirane
2-[2-(diethylamino)ethoxy] ethanol
N,N-diethyl hydroxy-8 F-octyl-8 dioxa-3,6 octylamine
Conditions | Yield |
---|---|
With sodium at 80 - 100℃; | 60% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 20h; | 56% |
silicon (IV) phthalocyanine dichloride
2-[2-(diethylamino)ethoxy] ethanol
Conditions | Yield |
---|---|
With sodium hydride In toluene at 20℃; Inert atmosphere; | 18.9% |
oxirane
2-[2-(diethylamino)ethoxy] ethanol
2-[2-(2-diethylamino-ethoxy)-ethoxy]-ethanol
Conditions | Yield |
---|---|
at 100℃; |
2-ethoxy-quinoline-4-carbonyl chloride
2-[2-(diethylamino)ethoxy] ethanol
Conditions | Yield |
---|---|
With benzene |
4-phenyltetrahydropyran-4-carbonyl chloride
2-[2-(diethylamino)ethoxy] ethanol
4-phenyl-tetrahydro-pyran-4-carboxylic acid-[2-(2-diethylamino-ethoxy)-ethyl ester]
Conditions | Yield |
---|---|
With toluene | |
With chloroform |
2-butoxy-4-quinolinecarbonyl chloride
2-[2-(diethylamino)ethoxy] ethanol
Conditions | Yield |
---|---|
With benzene |
2-pentyloxy-quinoline-4-carbonyl chloride
2-[2-(diethylamino)ethoxy] ethanol
Conditions | Yield |
---|---|
With benzene |
diphenylacetic acid chloride
2-[2-(diethylamino)ethoxy] ethanol
diphenyl-acetic acid-[2-(2-diethylamino-ethoxy)-ethyl ester]
1-phenylcyclohexylcarbonyl chloride
2-[2-(diethylamino)ethoxy] ethanol
UCB 597
cyclohexyl-phenyl-acetyl chloride
2-[2-(diethylamino)ethoxy] ethanol
cyclohexyl-phenyl-acetic acid-[2-(2-diethylamino-ethoxy)-ethyl ester]
1-phenylcyclopentanecarboxylic acid chloride
2-[2-(diethylamino)ethoxy] ethanol
carbetapentane
2-[2-(diethylamino)ethoxy] ethanol
acrylic acid methyl ester
1-acryloyloxy-2-(2-diethylamino-ethoxy)-ethane
Conditions | Yield |
---|---|
With 2,6-di-tert-butyl-4-methyl-phenol; benzene |
2-[2-(diethylamino)ethoxy] ethanol
methacrylic acid methyl ester
1-(2-diethylamino-ethoxy)-2-methacryloyloxy-ethane
Conditions | Yield |
---|---|
With N-Phenyl-2-naphthylamine; aluminum isopropoxide |
2-[2-(diethylamino)ethoxy] ethanol
acetylene
N,N-diethyl-2-(2-(vinyloxy)ethoxy)ethanamine
Conditions | Yield |
---|---|
With potassium hydroxide; benzene at 160℃; |
2-[2-(diethylamino)ethoxy] ethanol
2-<2-(diethylamino)ethoxy>ethyl chloride hydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride; thionyl chloride; chloroform | |
With thionyl chloride In benzene for 1.5h; Heating; |
1-azaphenothiazine-10-carbonyl chloride
2-[2-(diethylamino)ethoxy] ethanol
Conditions | Yield |
---|---|
In chlorobenzene Heating; |
biphenyl-4-yl-acetyl chloride
2-[2-(diethylamino)ethoxy] ethanol
<4>Biphenylylessigsaeure-<2-(2-diaethylamino-aethoxy)-aethylester>
Conditions | Yield |
---|---|
With pyridine In chloroform Heating; |
ethylamine
2-[2-(diethylamino)ethoxy] ethanol
(2-ethylamino-ethyl)-(2-diethylamino-ethyl)-ether
Conditions | Yield |
---|---|
(i) SOBr2, benzene, (ii) /BRN= 505933/, EtOH; Multistep reaction; |
2-[2-(diethylamino)ethoxy] ethanol
Propylpropargylacetat-2-(2'-diethylaminoethoxi)ethylester
Conditions | Yield |
---|---|
With potassium carbonate In toluene at 100℃; |
2-biphenyl-4-yl-butyryl chloride
2-[2-(diethylamino)ethoxy] ethanol
α-Aethyl-<4>biphenylylessigsaeure-<2-(2-diaethylamino-aethoxy)-aethylester>
Conditions | Yield |
---|---|
With pyridine In chloroform Heating; |
1-[2-(2-chloroethoxy)ethoxy]-2-methoxybenzene
2-[2-(diethylamino)ethoxy] ethanol
1-Diaethylamino-11-(2-methoxy-phenoxy)-3,6,9-trioxa-undecan
Conditions | Yield |
---|---|
(i) Na, xylene, (ii) /BRN= 2110861/; Multistep reaction; |
5-methyl-2-isopropylphenoxyethoxyethyl chloride
2-[2-(diethylamino)ethoxy] ethanol
1-Diethylamino-11-<6-isopropyl-3-methyl-phenoxy>-3,6,9-trioxa-undecan
Conditions | Yield |
---|---|
(i) Na, xylene, (ii) /BRN= 2267168/; Multistep reaction; |
α-(2,6-dimethylphenyl)-2,6-dimethylbenzenemethanol
2-[2-(diethylamino)ethoxy] ethanol
(2-{2-[Bis-(2,6-dimethyl-phenyl)-methoxy]-ethoxy}-ethyl)-diethyl-amine
Conditions | Yield |
---|---|
(i) HCl, benzene, (ii) /BRN= 506197/; Multistep reaction; |
Chemical Name: 6-Ethyl-3-oxa-6-azaoctanol
IUPAC NAME: 2-(2-diethylaminoethyloxy)ethanol
CAS No.: 140-82-9
EINECS: 205-436-7
Molecular Formula: C8H19NO2
Molecular Weight: 161.24 g/mol
Density: 0.939 g/cm3
Melting Point: 101°C
Flash Point: 95.8 °C
Boiling Point: 234.7 °C at 760 mmHg
Following is the structure of 2-(2-(DIETHYLAMINO)ETHOXY)ETHANOL(140-82-9):
The chemical synonymous of 2-(2-(DIETHYLAMINO)ETHOXY)ETHANOL(140-82-9) are 2-(2-(diethylamino)ethoxy)-ethano;2-(beta-(diethylamino)ethoxy)ethanol;2-[2-(diethylamino)ethoxy]-ethano;2-beta-Diethylaminoethoxyethanol;beta-(Diethylamino ethoxy)ethanol;Diethylaminoethoxyethanol;diethylaminoethoxyethanol,[combustibleliquidlabel];diethylaminoethoxyethanol,[flammableliquidlabel].
2-(2-(DIETHYLAMINO)ETHOXY)ETHANOL(140-82-9) is mainly used for the production of antitussives carbetapentane.
Product Categories about 2-(2-(DIETHYLAMINO)ETHOXY)ETHANOL(140-82-9) are Alkohols;Ethylene Glycols & Monofunctional Ethylene Glycols;Monofunctional Ethylene Glycols.
1. | skn-rbt 10 µL MLD open | NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0535166 . | ||
2. | eye-rbt 5 µL/24H SEV | NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0535166 . | ||
| ||||
|
rabbit | LD50 | skin | 2020uL/kg (2.02mL/kg) | GASTROINTESTINAL: OTHER CHANGES LIVER: OTHER CHANGES SKIN AND APPENDAGES (SKIN): "DERMATITIS, OTHER: AFTER SYSTEMIC EXPOSURE" | National Technical Information Service. Vol. OTS0535166, |
rat | LD50 | oral | 2590uL/kg (2.59mL/kg) | SENSE ORGANS AND SPECIAL SENSES: OTHER: EYE BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) GASTROINTESTINAL: OTHER CHANGES | National Technical Information Service. Vol. OTS0535166, |
A poison by ingestion and skin contact. A severe eye and mild skin irritant. When heated to decomposition it emits toxic vapors of NOx.
Safety Statements about 2-(2-(DIETHYLAMINO)ETHOXY)ETHANOL(140-82-9):
S23 Do not breathe vapour.
S24/25: Avoid contact with skin and eyes.
Health Hazard: Inhalation or contact with material may irritate or burn skin and eyes. Fire may produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control may cause pollution.
Fire Hazard: HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.
Reactivity Profile: 6-Ethyl-3-oxa-6-azaoctanol is an amine and alcohol. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.
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