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Cas:1118-68-9
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inquiryUnique advantages Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:White to slightly yellow crystalline powder Storage:cool dry place Package:1kg/foil bag;25kg/drum Application:phar
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inquiryProduct Name: N,N-Dimethylglycine Synonyms: DIMETHYLGLYCINE;DIMETHYLGLYCINE(N,N-);(DIMETHYLAMINO)ACETIC ACID;DMG;AKOS BB-5614;RARECHEM AL BO 0104;N,N-DIMETHYLAMINOACETIC ACID;N,N-DIMETHYLGLYCINE CAS: 1118-68-9 MF: C4H9NO2 MW: 103.12 EINECS: 21
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Cas:1118-68-9
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inquiryProduct Name: N,N-Dimthylglycine CAS NO.: 1118-68-9 Assay: >98% Water: ≤0.5% Ignition residue: ≤0.2%
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Cas:1118-68-9
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N,N-Dimethylglycine Basic information Description References
Cas:1118-68-9
Min.Order:1000 Kilogram
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Cas:1118-68-9
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Cas:1118-68-9
Min.Order:10 Gram
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inquirySuperior quality Appearance:white to slightly yellow crystalline powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Used as Pharmaceutical Int
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Cas:1118-68-9
Min.Order:1 Gram
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inquiryGMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol; water under 2068.6 Torr; for 10h; Ambient temperature; | 98% |
With sodium dihydrogenphosphate; zinc at 30℃; for 1h; | 94% |
With sodium tetrahydroborate In 2,2,2-trifluoroethanol for 24h; Reflux; | 91% |
N,N-dimethylglycine ethyl ester
dimethylaminoacetic acid
Conditions | Yield |
---|---|
With sodium hydroxide In water Heating; | 30% |
Conditions | Yield |
---|---|
With chromium(VI) oxide; sulfuric acid; acetone |
L-homocysteine
betaine
A
dimethylaminoacetic acid
B
L-methionine
Conditions | Yield |
---|---|
in Gegenwart von Leber-Praeparaten; |
Conditions | Yield |
---|---|
With potassium hydroxide at 100℃; |
2-dimethylaminomalonic acid diethyl ester
dimethylaminoacetic acid
Conditions | Yield |
---|---|
With hydrogenchloride |
Conditions | Yield |
---|---|
anschliessend Behandeln mit Barytwasser; |
Conditions | Yield |
---|---|
With hydrogenchloride; tin |
1-methyl-4-(phenylacetyl)pyridinium cation
dimethylaminoacetate
A
dimethylaminoacetic acid
B
C14H13NO
Conditions | Yield |
---|---|
In water at 25℃; Equilibrium constant; Rate constant; Thermodynamic data; ΔH0, ΔS0, ΔG0; kinetics, other temperatures; activation parameters: ΔH(excit.), ΔS(excit.), ΔG(excit.); |
3,5-dimethylphenyl (N,N-dimethylamino)acetate
A
dimethylaminoacetic acid
B
3,5-Dimethylphenol
Conditions | Yield |
---|---|
With sodium hydroxide; water In ethanol at 30℃; Rate constant; |
hydrogenchloride
formaldehyd
glycine
A
sarcosine
B
dimethylaminoacetic acid
formaldehyd
formic acid
glycine
A
dimethylaminoacetic acid
B
carbon dioxide
C
trimethylamine
formaldehyd
acetic acid
glycine
A
dimethylaminoacetic acid
B
carbon dioxide
C
trimethylamine
hydrogenchloride
formaldehyd
glycine
A
dimethylaminoacetic acid
B
rac-Ala-OH
Conditions | Yield |
---|---|
With hydrogenchloride at 150℃; under 661957 Torr; |
Conditions | Yield |
---|---|
Herstellung von -essigsaeure (Hydrochlorid. Krystalle (aus Eg.). F:187grad); |
Conditions | Yield |
---|---|
With Carbonate buffer Product distribution; controlled potential electrolysis: glassy-carbon plate electrode, pH 10; |
Conditions | Yield |
---|---|
With dihydroxyborane In dichloromethane at 20℃; for 48h; Petasis boronic acid-Mannich reaction; |
Conditions | Yield |
---|---|
With dihydroxyborane In dichloromethane at 20℃; for 48h; |
N,N-dimethylglycine sodium salt
dimethylaminoacetic acid
Conditions | Yield |
---|---|
With sulfuric acid In water at 50 - 80℃; pH=5 - 7; |
N,N-dimethylglycine methyl ester
N-methylhydroxyamine hydrochloride
A
dimethylaminoacetic acid
B
N-methyl-2-dimethylamino-acetohydroxamic acid
Conditions | Yield |
---|---|
With sodium hydroxide In tetrahydrofuran; water | |
With sodium hydroxide In water |
dimethylaminoacetic acid
Conditions | Yield |
---|---|
With Leisingera caerulea TmpB oxygenase; oxygen; sodium L-ascorbate In aq. buffer at 0.3℃; for 4h; pH=7.5; Enzymatic reaction; |
Conditions | Yield |
---|---|
With Ru on activatedcarbon cloth; activatedcarbon cloth In aq. phosphate buffer at 60℃; for 10h; pH=7.5; Electrochemical reaction; |
dimethylaminoacetic acid
(piperidin-4-yl)carbamic acid tert-butyl ester
tert-butyl [1-(2-dimethylaminoacetyl)piperidin-4-yl]carbamate
Conditions | Yield |
---|---|
Stage #1: dimethylaminoacetic acid; (piperidin-4-yl)carbamic acid tert-butyl ester With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 46h; Stage #2: With sodium hydroxide In water; ethyl acetate; N,N-dimethyl-formamide; sodium chloride at 20℃; for 0.5h; | 100% |
With sodium hydroxide; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 46h; | 100% |
tert-butyl 5-amino-2,3-dihydro-1H-indole-1-carboxylate
dimethylaminoacetic acid
tert-butyl 5-[(N,N-dimethylglycyl)amino]-1-indolinecarboxylate
Conditions | Yield |
---|---|
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; triethylamine In DMF (N,N-dimethyl-formamide) for 0.166667h; | 100% |
dimethylaminoacetic acid
4-aminomethyl-4-[3-(1-methyl-1H-pyrazol-4-yl)-phenyl]-piperidine-1-carboxylic acid tert-butyl ester
tert-butyl 4-((2-(dimethylamino)acetamido)methyl)-4-(3-(1-methyl-1H-pyrazol-4-yl)phenyl)piperidine-1-carboxylate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 20℃; for 4h; | 100% |
dimethylaminoacetic 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 tetrahydrofuran Inert atmosphere; | 100% |
dimethylaminoacetic acid
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; | 100% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; | 100% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; | 100% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; | 100% |
dimethylaminoacetic acid
Conditions | Yield |
---|---|
Stage #1: dimethylaminoacetic acid 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 tetrahydrofuran at 0℃; for 0.166667h; Stage #2: 4-(6-fluoro-1-(phenylsulfonyl)-1H-indol-3-yl)benzene-1,2-diamine In tetrahydrofuran at 20℃; for 1h; | 100% |
dimethylaminoacetic acid
Conditions | Yield |
---|---|
Stage #1: dimethylaminoacetic acid With N-ethyl-N,N-diisopropylamine; HATU In dichloromethane at 20℃; for 0.00333333h; Inert atmosphere; Stage #2: 8-methyl-7-[4-(4-piperidyloxy)phenyl]quinoline In dichloromethane at 20℃; | 99% |
dimethylaminoacetic acid
Conditions | Yield |
---|---|
With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; | 99% |
Conditions | Yield |
---|---|
98% |
dimethylaminoacetic acid
3-azidopropylamine
N-(3-azidopropyl)-2-(dimethylamino)-acetamide
Conditions | Yield |
---|---|
With 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In N,N-dimethyl-formamide at 0 - 20℃; for 7.58333h; | 98% |
Conditions | Yield |
---|---|
In ethyl acetate at 20℃; for 2h; Inert atmosphere; Schlenk technique; | 98% |
Conditions | Yield |
---|---|
Stage #1: dimethylaminoacetic acid With triethylamine In dichloromethane at 0℃; for 0.166667h; Stage #2: 2,3,5,6-tetraflourophenol With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 20℃; for 5h; | 98% |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 20h; | 97% |
dimethylaminoacetic acid
(S,S)-N,N'-dimethyl-1,2-diphenylethane-1,2-diamine
N,N'-[(1S,2S)-1,2-diphenylethane-1,2-diyl] bis[2-(dimethylamino)-N-methylacetamide]
Conditions | Yield |
---|---|
Stage #1: dimethylaminoacetic acid With chloroformic acid ethyl ester; triethylamine In dichloromethane at 0℃; for 0.5h; Inert atmosphere; Stage #2: (S,S)-N,N'-dimethyl-1,2-diphenylethane-1,2-diamine In dichloromethane at 0℃; for 12h; Inert atmosphere; | 97% |
Conditions | Yield |
---|---|
Stage #1: dimethylaminoacetic acid With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 1h; Stage #2: C10H13N3O3 In N,N-dimethyl-formamide at 20 - 80℃; for 6h; | 96.37% |
tert-butyl 5-(2-(3-aminophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate
dimethylaminoacetic acid
tert-butyl 5-(2-(3-(2-(dimethylamino)acetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate
Conditions | Yield |
---|---|
Stage #1: dimethylaminoacetic acid With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 0.166667 - 0.25h; Stage #2: tert-butyl 5-(2-(3-aminophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate In dichloromethane at 20℃; for 17.5h; | 96% |
Stage #1: dimethylaminoacetic acid With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 0.25h; Stage #2: tert-butyl 5-(2-(3-aminophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate In dichloromethane at 20℃; for 17.5h; | 96% |
Stage #1: dimethylaminoacetic acid With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 0.166667 - 0.25h; Stage #2: tert-butyl 5-(2-(3-aminophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate In dichloromethane at 20℃; for 1.5h; Stage #3: dimethylaminoacetic acid With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 16h; | 96% |
dimethylaminoacetic acid
(3aR,7S,7aS)-7-(4-amino-3-fluorobenzyl)-3-(3-(tert-butyl)benzyl)hexahydro-2H-thiopyrano[3,4-d]oxazol-2-one 5,5-dioxide
N-(4-(((3aR,7S,7aS)-3-(3-(tert-butyl)benzyl)-5,5-dioxido-2-oxohexahydro-2H-thiopyrano[3,4-d]oxazol-7-yl)methyl)-2-fluorophenyl)-2-(dimethylamino) acetamide
Conditions | Yield |
---|---|
With 4-methyl-morpholine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide In N,N-dimethyl-formamide at 25℃; for 19h; Inert atmosphere; | 96% |
dimethylaminoacetic acid
Conditions | Yield |
---|---|
With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 1h; Inert atmosphere; | 96% |
With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 1h; Time; Inert atmosphere; | 96% |
methyl 4'-{[(3-aminopyridin-2-yl)amino]methyl}-biphenyl-2-carboxylate
dimethylaminoacetic acid
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride | 95% |
dimethylaminoacetic acid
(+)-B-methoxydiisocamphenylborane
Conditions | Yield |
---|---|
In tetrahydrofuran; ethanol; water dropwise addn. of 1 M soln. of (+)(C10H17)2BOCH3 in THF to N,N-dimethylglycine in ethanol/H2O (1:1), stirring at 80-100°C; control of completion of the reaction by (11)B-NMR, removing of solvent under vacuum (1-2.0 mm), treating with methanol, obtaining viscous liquid; | 95% |
In tetrahydrofuran; dimethyl sulfoxide dropwise addn. of 1 M soln. of (+)(C10H17)2BOCH3 in THF to N,N-dimethylglycine in DMSO, stirring at 80-100°C; control of completion of the reaction by (11)B-NMR, removing of solvent under vacuum (1-2.0 mm), treating with methanol, obtaining viscous liquid; | 95% |
dimethylaminoacetic acid
B-methoxydicyclohexylborane
(C6H11)2BOCOCH2N(CH3)2
Conditions | Yield |
---|---|
In tetrahydrofuran; dimethyl sulfoxide dropwise addn. of 1 M soln. of (C6H11)2BOCH3 in THF to N,N-dimethylglycine in DMSO, stirring at 80-100°C; control of completion of the reaction by (11)B-NMR, removing of solvent under vacuum (1-2.0 mm), treating with methanol, obtaining viscous liquid; | 95% |
In tetrahydrofuran; ethanol; water dropwise addn. of 1 M soln. of (C6H11)2BOCH3 in THF to N,N-dimethylglycine in ethanol/H2O (1:1), stirring at 80-100°C; control of completion of the reaction by (11)B-NMR, removing of solvent under vacuum (1-2.0 mm), treating with methanol, obtaining viscous liquid; | 95% |
4-(4-iodophenoxy)piperidine
dimethylaminoacetic acid
2-(dimethylamino)-1-(4-(4-iodophenoxy)piperidin-1-yl)ethanone
Conditions | Yield |
---|---|
With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; | 95% |
dimethylaminoacetic acid
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 4h; | 95% |
tert-butyl [2-amino-2-(hydroxyimino)ethyl]carbamate
dimethylaminoacetic acid
Conditions | Yield |
---|---|
Stage #1: dimethylaminoacetic acid With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 1h; Stage #2: tert-butyl [2-amino-2-(hydroxyimino)ethyl]carbamate In N,N-dimethyl-formamide at 20 - 80℃; for 6h; | 94.99% |
dimethylaminoacetic acid
(-)-B-methoxydiisopinocampheylborane
Conditions | Yield |
---|---|
In tetrahydrofuran; ethanol; water dropwise addn. of 1 M soln. of (-)(C10H17)2BOCH3 in THF to N,N-dimethylglycine in ethanol/H2O (1:1), stirring at 80-100°C; control of completion of the reaction by (11)B-NMR, removing of solvent under vacuum (1-2.0 mm), treating with methanol, obtaining viscous liquid; | 94% |
In tetrahydrofuran; dimethyl sulfoxide dropwise addn. of 1 M soln. of (-)(C10H17)2BOCH3 in THF to N,N-dimethylglycine in DMSO, stirring at 80-100°C; control of completion of the reaction by (11)B-NMR, removing of solvent under vacuum (1-2.0 mm), treating with methanol, obtaining viscous liquid; | 94% |
dimethylaminoacetic acid
2,3,4,5,6-pentafluorophenol
dimethylamino-acetic acid pentafluorophenyl ester
Conditions | Yield |
---|---|
Stage #1: dimethylaminoacetic acid With triethylamine In dichloromethane at 0℃; for 0.166667h; Stage #2: 2,3,4,5,6-pentafluorophenol With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 20℃; for 5h; | 94% |
With dicyclohexyl-carbodiimide In ethyl acetate at 20℃; for 12h; | |
With diisopropyl-carbodiimide In ethyl acetate at 20℃; for 12h; | |
With dicyclohexyl-carbodiimide In ethyl acetate |
dimethylaminoacetic acid
N-(8-hydroxyoctyl)carbamic acid tert-butyl ester
8-(t-butoxycarbonylamino)octyl 2-(dimethylamino)acetate
Conditions | Yield |
---|---|
With 4-methyl-morpholine; dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane | 94% |
dimethylaminoacetic acid
(10-hydroxydecyl)carbamic acid tert-butyl ester
10-(t-butoxycarbonylamino)decyl 2-(dimethylamino)acetate
Conditions | Yield |
---|---|
With 4-methyl-morpholine; dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane | 94% |
Conditions | Yield |
---|---|
Stage #1: dimethylaminoacetic acid With bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine In dichloromethane at 0 - 20℃; for 0.5h; Stage #2: 2-demethylcolchicine In dichloromethane for 18h; | 93% |
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