As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
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inquiryProduct Description Product website: http://www.finerchem.com Product Name N-Methyl-N-(N,N-dimethylaminoethyl)-aminoethanol
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inquiryProduct Name: N,N,N′-triemthylaminoethyl-N′-methylaminoehylanol Molecular Formula: C7H18N2O Molecular Weight: 146 CAS RN: 2212-32-0 Properties: N,N,N′-triemthylaminoethyl-N′-methylaminoehylanol is colorless to light yel
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inquiryN-Methyl-N-(N,N-dimethylaminoethyl)-aminoethanol CAS:2212-32-0 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing i
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
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inquiryProduct Detail Minimum Order Qty. 10 Gram
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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inquiryBest quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
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inquiry1. We can provide customers with "one-stop"packaging service,from research,development,production,export and so on 2. Powerful R&D strength let our technology in a leading level,forever,in turn,to provide customers with better service .
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Cas:2212-32-0
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inquiryProduct name: 2-((2-(Dimethylamino)ethyl)Methylamino)-ethanol CAS No.: 2212-32-0 Molecule Formula:C7H18N2O Molecule Weight:146.23 Purity: 99.0% Package: 180kg/drum Description:Colorless liquid Manufacture Standards:Enterprise Standard
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inquiry★.Best quality according to requirement ★.Competitive price in China market ★.Mature Technical support ★.Professional logistic support ★.Shortest delivery time . Appearance:Refer to COA Storage:Store in dry, cool and ventilated place Package:Acc
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inquiryfactory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
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inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
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inquiryformaldehyd
2-(2-Aminoethylamino)ethanol
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
Conditions | Yield |
---|---|
Stage #1: formaldehyd; 2-(2-Aminoethylamino)ethanol at 80 - 90℃; for 0.5h; Stage #2: With formic acid at 80 - 90℃; for 2h; Stage #3: In butan-1-ol at 120℃; for 4h; Temperature; Solvent; | 95.2% |
With 5%-palladium/activated carbon; hydrogen at 100 - 110℃; under 11251.1 Torr; for 4.5h; Reagent/catalyst; Temperature; Pressure; Inert atmosphere; Autoclave; | 90.4% |
With formic acid In water for 4h; Heating; | 70% |
With formic acid |
(2-hydroxyethyl)(methyl)amine
2-(dimethylamino)ethyl chloride
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
Conditions | Yield |
---|---|
With potassium carbonate In ethanol Heating; |
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
Conditions | Yield |
---|---|
In toluene the aminoalcohol is added to a soln. of Ce(OiPr)4 in toluene at room temp, stirring for 12 h (under argon using Schlenk tubes); evapn. to dryness, the crude product is recrystd. in a mixt. of toluene and CH2Cl2, crystals are obtained at -30°C, elem. anal.; | 96% |
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
Conditions | Yield |
---|---|
In hexane byproducts: HN(Si(CH3)3)2; under dry N2; alcohol added to soln. of Zn-compd., exothermic reaction, stirred for 16h,; volatiles removed in vac., solidified on standing for 1-2d; elem. anal.; | 95% |
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
Conditions | Yield |
---|---|
In toluene the aminoalcohol is added to a soln. of Ce(OiPr)4 (ratio 2:1) in toluene at room temp, stirring for 12 h (under argon using Schlenk tubes); isolated by concentration from the reaction medium, elem. anal.; | 95% |
Conditions | Yield |
---|---|
Stage #1: 2-{[2-(dimethylamino)ethyl]methylamino}ethanol With sodium hydride In tetrahydrofuran at -20℃; for 1h; Inert atmosphere; Schlenk technique; Stage #2: carbon disulfide In tetrahydrofuran for 1h; Inert atmosphere; Schlenk technique; | 91% |
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at 20℃; for 16h; Inert atmosphere; | 88% |
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at 20℃; for 16h; Inert atmosphere; | 85% |
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
Conditions | Yield |
---|---|
With n-butyllithium In hexane at -40 - 20℃; for 4h; Schlenk technique; Inert atmosphere; | 85% |
With n-butyllithium In hexane at -40 - 20℃; for 4h; Schlenk technique; Glovebox; Inert atmosphere; | 85% |
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
copper(II) methoxide
Conditions | Yield |
---|---|
In not given prepd. by the alcohol-exchange procedure described by Singh, J. V.; Baranwal, B. P.; Mehrotra, R. C.; T. Anorg. Allg. Chem. 1981, 477, 235; crystn. from hexane and distn. of mother liquor; | 83% |
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
phthalocyanine silicon(IV) dichloride
C46H50N12O2Si
Conditions | Yield |
---|---|
With pyridine In toluene for 4h; Reflux; | 81% |
With pyridine In toluene for 36h; Reflux; Inert atmosphere; | 81% |
Conditions | Yield |
---|---|
In hexane at -78 - 20℃; Inert atmosphere; | 79% |
Conditions | Yield |
---|---|
In hexane at -78 - 50℃; Inert atmosphere; Schlenk technique; | 77% |
Conditions | Yield |
---|---|
In toluene for 12h; Reflux; Inert atmosphere; | 76% |
4-Nitrophthalonitrile
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
Conditions | Yield |
---|---|
Stage #1: 4-Nitrophthalonitrile; 2-{[2-(dimethylamino)ethyl]methylamino}ethanol In N,N-dimethyl-formamide at 35℃; for 0.25h; Inert atmosphere; Stage #2: With potassium carbonate In N,N-dimethyl-formamide at 35℃; for 144h; Inert atmosphere; | 74% |
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at 20℃; | 72% |
Conditions | Yield |
---|---|
In hexane at -78 - 20℃; for 1h; Inert atmosphere; Schlenk technique; | 72% |
Conditions | Yield |
---|---|
With triethylamine In methanol at 20℃; for 2h; | 69% |
Conditions | Yield |
---|---|
With triethylamine In methanol at 20℃; for 2h; | 60% |
Conditions | Yield |
---|---|
With triethylamine In methanol at 20℃; for 2h; | 60% |
Conditions | Yield |
---|---|
With triethylamine In methanol at 20℃; for 2h; | 59% |
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
tetra[3-(dimethylchlorosilyl)propyl]silane
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at 20℃; | 57% |
Conditions | Yield |
---|---|
With triethylamine In methanol at 20℃; for 2h; | 57% |
Conditions | Yield |
---|---|
With triethylamine In methanol at 20℃; for 2h; | 56% |
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
propargyl bromide
N,N,N'-trimethyl-N'-(2-(prop-2-inyloxy)ethyl)ethano-1,2-diamine
Conditions | Yield |
---|---|
Stage #1: 2-{[2-(dimethylamino)ethyl]methylamino}ethanol With sodium hydride In tetrahydrofuran; hexane at -30℃; Inert atmosphere; Stage #2: propargyl bromide In tetrahydrofuran; hexane; toluene at -30 - 20℃; Inert atmosphere; | 51% |
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
Conditions | Yield |
---|---|
In acetonitrile Fe-compound reacted with organic ligand in 1:2 molar ratio in MeCN; | 45% |
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide at 0℃; for 3h; | 43% |
sodium benzoate
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
acetonitrile
Conditions | Yield |
---|---|
In acetonitrile (under aerobic conditions); soln. of Fe-complex and sodium benzoate in MeCN treated with ligand, stirred for few h; filtered, allowed to stand at room temp. for 3 d; | 40% |
sodium benzoate
2-{[2-(dimethylamino)ethyl]methylamino}ethanol
acetonitrile
Conditions | Yield |
---|---|
In acetonitrile byproducts: NaCl; (under aerobic conditions); soln. of FeCl3*6H2O and sodium benzoate in MeCN treated with ligand, stirred for 3 h; filtered, left at room temp. for 5 d; | 30% |
Conditions | Yield |
---|---|
With NEt3 In methanol; acetonitrile 2-(2-((dimethylamino)ethyl)methylamino)ethanol, sodium pivalate, NEt3, added to MeCN/MeOH soln. of Mn(NO3)2, Gd(NO3)3; stirred for 3 h; filtered; crystd. by Et2O diffusion after 2 d; filtered; washed with Et2O; vac. dried; elem. anal.; | 20% |
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