CAS No.13200-60-7,ethyl 2-(methylamino)acetate Suppliers

Dayang Chem (Hangzhou) Co.,Ltd.

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Glycine, N-methyl-, ethyl ester

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Hebei Nengqian Chemical Import and Export Co., LTD

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ethyl 2-(methylamino)acetate

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Shanghai Upbio Tech Co.,Ltd

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Glycine, N-methyl-, ethyl ester

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Hangzhou J&H Chemical Co., Ltd.

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Zibo Hangyu Biotechnology Development Co., Ltd

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Glycine, N-methyl-, ethyl ester

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Henan Tianfu Chemical Co., Ltd.

Our company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O

13200-60-7 ethyl 2-(methylamino)acetate

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Xi`an Eastling Biotech Co., Ltd.

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ethyl 2-(methylamino)acetate

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Glycine, N-methyl-, ethyl ester

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Hangzhou Fandachem Co.,Ltd

Glycine, N-methyl-, ethyl ester cas 13200-60-7Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

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ETHYL 2-(METHYLAMINO)ACETATE

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Ethyl 2-(methylamino)acetate

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Nanjing Chemlin Chemical Co., Ltd.

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Chemical Technology Co.,LTD

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ethyl 2-(methylamino)acetate

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Debye Scientific

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ethyl 2-(methylamino)acetate

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Synthetic route

: 105-36-2
ethyl bromoacetate

: 74-89-5
methylamine

: 13200-60-7
Sarcosine ethyl ester

Conditions

Conditions	Yield
In acetonitrile at 0 - 20℃;	85%
In diethyl ether; benzene

: 107-97-1
sarcosine

: 64-17-5
ethanol

: 13200-60-7
Sarcosine ethyl ester

Conditions

Conditions	Yield
With hydrogenchloride for 2h; Heating;	80%
With thionyl chloride for 5h; Reflux;	65%
With hydrogenchloride

: 64-17-5
ethanol

: 131543-46-9
Glyoxal

: 74-89-5
methylamine

A: 44565-47-1
N1,N2-dimethylglycinamide

B: 13200-60-7
Sarcosine ethyl ester

Conditions

Conditions	Yield
im Rohr; reagiert analog mit anderen Alkyl- und Dialkylaminen;

...Expand

: 64-17-5
ethanol

: 5616-32-0
(methylamino)acetonitrile

: 13200-60-7
Sarcosine ethyl ester

Conditions

Conditions	Yield
With hydrogenchloride

: 50-00-0
formaldehyd

: 151-50-8
potassium cyanide

methylamine sulfate: methylamine sulfate

: 13200-60-7
Sarcosine ethyl ester

Conditions

Conditions	Yield
With water unter Einleiten von Kohlendioxyd und Kochen des entstandenen Nitrils mit alkoh. Salzsaeure auf dem Wasserbad;

...Expand

: 64-17-5
ethanol

: 74-89-5
methylamine

polyglyoxal: polyglyoxal

A: 44565-47-1
N1,N2-dimethylglycinamide

B: 13200-60-7
Sarcosine ethyl ester

...Expand

: 52605-49-9
sarcosine ethyl ester hydrochloride

: 121-44-8
triethylamine

A: 13200-60-7
Sarcosine ethyl ester

B: 554-68-7
triethylamine hydrochloride

Conditions

Conditions	Yield
In dichloromethane

...Expand

: 145060-76-0
tert-butoxycarbonyl-methyl-amino-acetic acid ethyl ester

: 13200-60-7
Sarcosine ethyl ester

Conditions

Conditions	Yield
With trifluoroacetic acid In dichloromethane at 0 - 20℃;

: 52605-49-9
sarcosine ethyl ester hydrochloride

: 13200-60-7
Sarcosine ethyl ester

Conditions

Conditions	Yield
With water
In water

: 593-51-1
methylamine hydrochloride

: 105-39-5
chloroacetic acid ethyl ester

: 13200-60-7
Sarcosine ethyl ester

Conditions

Conditions	Yield
Stage #1: methylamine hydrochloride With potassium carbonate In acetonitrile at 15℃; for 1.5h; Stage #2: chloroacetic acid ethyl ester In acetonitrile at 20℃; for 10h;
With potassium carbonate In acetonitrile at 20℃; for 10h;
Stage #1: methylamine hydrochloride With triethylamine In acetonitrile at 15℃; for 1.5h; Stage #2: chloroacetic acid ethyl ester In acetonitrile at 20℃; for 10h;

: 459-73-4
GlyOEt*HCl

: 333-27-7
methyl trifluoromethanesulfonate

: 13200-60-7
Sarcosine ethyl ester

Conditions

Conditions	Yield
With 1,1,1,3',3',3'-hexafluoro-propanol at 20℃; for 1h;

: 13200-60-7
Sarcosine ethyl ester

: 99-61-6
3-nitro-benzaldehyde

: 892414-09-4
C12H16N2O4

Conditions

Conditions	Yield
Stage #1: Sarcosine ethyl ester; 3-nitro-benzaldehyde With titanium(IV) isopropylate In 1,2-dichloro-ethane at 20℃; for 0.166667h; Stage #2: With sodium tris(acetoxy)borohydride In 1,2-dichloro-ethane at 20℃; for 2h;	100%

: 13200-60-7
Sarcosine ethyl ester

: 24424-99-5
di-tert-butyl dicarbonate

: 145060-76-0
tert-butoxycarbonyl-methyl-amino-acetic acid ethyl ester

Conditions

Conditions	Yield
With triethylamine In dichloromethane for 66h;	100%
With sodium hydrogencarbonate In water at 20℃;	89%

: 928150-02-1
7-chloro-3-[(5-chloromethyl)-([1,2,4]oxadiazol-3-yl)]-1-(tetrahydropyran-4-yl)methyl-1H-indole

: 13200-60-7
Sarcosine ethyl ester

: 1292847-34-7
C22H27ClN4O4

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In acetonitrile at 60℃; for 18h;	100%

: 13200-60-7
Sarcosine ethyl ester

: 931-59-9
benzenesulfenyl chloride

: 180253-99-0
(Methyl-phenylsulfanyl-amino)-acetic acid ethyl ester

Conditions

Conditions	Yield
With triethylamine In diethyl ether at 0℃; for 1h;	99%

: 13200-60-7
Sarcosine ethyl ester

: 52119-38-7
ethyl 3-oxo-3-(3-nitrophenyl)propanoate

: 1-methyl-3-(α-hydroxy-3'-nitrobenzylidene)pyrrolidine-2,4-dione

Conditions

Conditions	Yield
Stage #1: Sarcosine ethyl ester; ethyl 3-oxo-3-(3-nitrophenyl)propanoate In xylene at 125 - 130℃; for 20h; Stage #2: With sodium methylate In methanol; xylene at 20℃; for 48h;	98.2%

: 13200-60-7
Sarcosine ethyl ester

: 38002-87-8
O-methallylsalicylaldehyde

: (2RS,3aSR,9bRS)-2-ethoxycarbonyl-1,2,3,3a,4,9b-hexahydro-1,3a-dimethyl[1]benzopyrano[4,3-b]pyrrole

Conditions

Conditions	Yield
In xylene at 130℃; for 0.5h; microwave irradiation;	98%

: 13200-60-7
Sarcosine ethyl ester

: 83611-34-1
ethyl (E)-4-(2-formylphenoxy)but-2-enoate

: 1-methyl-1,2,3,3a,4,9b-hexahydro-5-oxa-1-aza-cyclopenta[a]naphthalene-2,3-dicarboxylic acid diethyl ester

Conditions

Conditions	Yield
at 130℃; for 0.0833333h; microwave irradiation;	98%

: 229342-64-7
3-chloro-N-(4-chloro-2-{[(4-chlorophenyl)amino]carbonyl}phenyl)-4-(chloromethyl)-2-thiophenecarboxamide

: 13200-60-7
Sarcosine ethyl ester

: C24H22Cl3N3O4S

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 0 - 20℃;	98%

: 13200-60-7
Sarcosine ethyl ester

: 34893-92-0
3,4-dichlorophenyl isocyanate

: 27387-90-2
3-(3,5-dichlorophenyl)-1-methyl-2,4-imidazolidinedione

Conditions

Conditions	Yield
With sodium hydroxide In tetrahydrofuran; water Inert atmosphere;	96%
With sodium hydroxide In tetrahydrofuran; water	96%

: 108-77-0
1,3,5-trichloro-2,4,6-triazine

: 13200-60-7
Sarcosine ethyl ester

: ethyl N-(4,6-dichloro-1,3,5-triazin-2-yl)-N-methylglycinate

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In acetone at 0℃; for 2h;	94%
In tetrahydrofuran; ethyl acetate at -2℃; for 0.25h;
In tetrahydrofuran; ethyl acetate at -2℃;

: 13200-60-7
Sarcosine ethyl ester

: 1394067-24-3
1-{2-[(1S,4S)-5-(tert-butoxycarbonyl)-2,5-diazabicyclo[2.2.1]hept-2-yl]pyridin-4-yl}-3-(pyrazin-2-ylamino)-1H-indazole-6-carboxylic acid

: ethyl N-{[1-{2-[(1S,4S)-2,5-diazabicyclo[2.2.1]hept-2-yl]pyridin-4-yl}-3-(pyrazin-2-ylamino)-1H-indazol-6-yl]carbonyl}-N-methylglycinate

Conditions

Conditions	Yield
Stage #1: 1-{2-[(1S,4S)-5-(tert-butoxycarbonyl)-2,5-diazabicyclo[2.2.1]hept-2-yl]pyridin-4-yl}-3-(pyrazin-2-ylamino)-1H-indazole-6-carboxylic acid With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 3h; Stage #2: Sarcosine ethyl ester In N,N-dimethyl-formamide at 20℃;	94%

: 13200-60-7
Sarcosine ethyl ester

: 96601-09-1
5-nitro-2-(prop-2-en-1-yloxy)benzaldehyde

: ethyl (2RS,3aSR,9bRS)-1-methyl-8-nitro-1,2,3,3a,4,9b-hexahydrochromeno[4,3-b]pyrrole-2-carboxylate

Conditions

Conditions	Yield
In neat (no solvent, solid phase) for 0.166667h; Microwave irradiation; Green chemistry;	94%

: 50-00-0
formaldehyd

: 1631-28-3
N-p-tolylphenylmaleimide

: 13200-60-7
Sarcosine ethyl ester

: 106369-04-4, 106402-32-8
(3aS,6aR)-2-Methyl-4,6-dioxo-5-p-tolyl-octahydro-pyrrolo[3,4-c]pyrrole-1-carboxylic acid ethyl ester

Conditions

Conditions	Yield
In toluene for 1h; Heating; Dean-Stark trap;	93%

...Expand

: 28752-82-1
2-(allyloxy)benzaldehyde

: 13200-60-7
Sarcosine ethyl ester

: (3aR,9bR)-1-Methyl-1,2,3,3a,4,9b-hexahydro-chromeno[4,3-b]pyrrole-2-carboxylic acid ethyl ester

: ethyl (2RS,3aSR,9bRS)-1-methyl-1,2,3,3a,4,9b-hexahydrochromeno[4,3-b]pyrrole-2-carboxylate

Conditions

Conditions	Yield
at 130℃; for 0.25h; microwave irradiation;	A n/a B 93%

...Expand

: 28809-06-5
2-[(E)-(3-phenyl-2-propenyl)oxy]benzaldehyde

: 13200-60-7
Sarcosine ethyl ester

: (3aRS,9bRS)-2-ethoxycarbonyl-1,2,3,3a,4,9b-hexahydro-1-methyl-3-phenyl[1]benzopyrano[4,3-b]pyrrole

: (2RS,3RS,3aSR,9bRS)-2-ethoxycarbonyl-1,2,3,3a,4,9b-hexahydro-1-methyl-3-phenyl[1]benzopyrano[4,3-b]pyrrole

Conditions

Conditions	Yield
In toluene for 4h; Heating;	A n/a B 93%

...Expand

: 13200-60-7
Sarcosine ethyl ester

: 462094-45-7
2-[(2-oxo-2H-chromen-4-yl)oxy]acetic acid

: ethyl 2-(N-methyl-2-(2-oxo-2H-chromen-4-yloxy)acetamido)acetate

Conditions

Conditions	Yield
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 0 - 25℃; for 8h;	92.7%

: (2S)-2-[(tert-Butoxycarbonyl)amino]-3-{[(2-nitrophenyl)sulfonyl]amino}propionic Acid

: 13200-60-7
Sarcosine ethyl ester

: 25952-53-8
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride

: {[(S)-2-tert-Butoxycarbonylamino-3-(2-nitro-benzenesulfonylamino)-propionyl]-methyl-amino}-acetic acid ethyl ester

Conditions

Conditions	Yield
With benzotriazol-1-ol In chloroform; water; ethyl acetate; N,N-dimethyl-formamide	91%

...Expand

: (2S)-2-[(tert-Butoxycarbonyl)amino]-3-{[(2-nitrophenyl)sulfonyl]amino}propionic Acid

: 13200-60-7
Sarcosine ethyl ester

: 1276121-84-6
{[(S)-2-tert-butoxycarbonylamino-3-(2-nitrobenzenesulfonylamino)propionyl]methylamino}acetic acid ethyl ester

Conditions

Conditions	Yield
Stage #1: (2S)-2-[(tert-Butoxycarbonyl)amino]-3-{[(2-nitrophenyl)sulfonyl]amino}propionic Acid With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at -10℃; for 0.5h; Stage #2: Sarcosine ethyl ester In chloroform; N,N-dimethyl-formamide at -10 - 20℃;	91%
Stage #1: (2S)-2-[(tert-Butoxycarbonyl)amino]-3-{[(2-nitrophenyl)sulfonyl]amino}propionic Acid With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at -10℃; for 0.5h; Stage #2: Sarcosine ethyl ester In chloroform; N,N-dimethyl-formamide at -10 - 20℃; for 1h;	91%
Stage #1: (2S)-2-[(tert-Butoxycarbonyl)amino]-3-{[(2-nitrophenyl)sulfonyl]amino}propionic Acid With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at -10℃; for 0.5h; Stage #2: Sarcosine ethyl ester In chloroform; N,N-dimethyl-formamide at 20℃; for 1h;	91%

: 13200-60-7
Sarcosine ethyl ester

: C10H19BrO2

: C15H29NO4

Conditions

Conditions	Yield
With potassium carbonate In acetone at 140℃; for 14h; Microwave irradiation;	91%

: 13200-60-7
Sarcosine ethyl ester

: 180253-97-8
2-Benzyloxycarbonylamino-2-methyl-propionic acid 2-thioxo-2H-pyridin-1-yl ester

: 180254-00-6
[N-[N'-(2-benzyloxycarbonyl)amino-2-methylpropionyl]-N-methylamino]acetic acid ethyl ester

Conditions

Conditions	Yield
With triethylamine In dichloromethane for 12h; Ambient temperature;	90%

: 13200-60-7
Sarcosine ethyl ester

: 152842-93-8
5-chloro-2-prop-2-enyloxybenzaldehyde

: 8-chloro-1-methyl-1,2,3,3a,4,9b-hexahydro-5-oxa-1-aza-cyclopenta[a]naphthalene-2-carboxylic acid ethyl ester

: 8-chloro-1-methyl-1,2,3,3a,4,9b-hexahydro-5-oxa-1-aza-cyclopenta[a]naphthalene-2-carboxylic acid ethyl ester

Conditions

Conditions	Yield
In toluene for 4h; Heating;	A n/a B 90%

...Expand

polymer, [poly(ethylene glycol)-O-CO]2LysOSu, M = 20 kDa: polymer, [poly(ethylene glycol)-O-CO]2LysOSu, M = 20 kDa

: 13200-60-7
Sarcosine ethyl ester

polymer, [poly(ethylene glycol)-O-CO]2Lys-Sar-OEt, M = 20 kDa: polymer, [poly(ethylene glycol)-O-CO]2Lys-Sar-OEt, M = 20 kDa

Conditions

Conditions	Yield
With triethylamine In chloroform at 20℃; for 12h; pH=8;	90%

: 13200-60-7
Sarcosine ethyl ester

: 1559069-47-4
C5H5Br2N3*BrH

: C10H15BrN4O2

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl-formamide at 120℃; for 0.333333h;	90%

: 13200-60-7
Sarcosine ethyl ester

: 92345-90-9
3,4-dimethoxy-2-allylbenzaldehyde

: 92345-91-0
(2R,3aS,8bR)-5,6-Dimethoxy-1-methyl-1,2,3,3a,4,8b-hexahydro-indeno[1,2-b]pyrrole-2-carboxylic acid ethyl ester

Conditions

Conditions	Yield
In toluene Heating;	89%

: 13200-60-7
Sarcosine ethyl ester

: 582-61-6
benzoyl azide

: 2221-12-7
1-methyl-3-phenyl-2,4-imidazolidinedione

Conditions

Conditions	Yield
With potassium carbonate at 100℃; for 8h;	89%

: 13200-60-7
Sarcosine ethyl ester

: 63005-36-7
methyl 2-(bromomethyl)-4,5-dimethoxybenzoate

: 112434-97-6
N-(2-carboethoxy-4,5-dimethoxybenzyl)sarcosine methyl ester

Conditions

Conditions	Yield
With sodium carbonate In toluene at 85℃; for 3.5h;	87%

: 13200-60-7
Sarcosine ethyl ester

: 100-52-7
benzaldehyde

: 624-49-7
dimethylfumarate

A: 1-Methyl-5-phenyl-pyrrolidine-2,3,4-tricarboxylic acid 2-ethyl ester 3,4-dimethyl ester

: (2R,3R,4R,5R)-1-Methyl-5-phenyl-pyrrolidine-2,3,4-tricarboxylic acid 2-ethyl ester 3,4-dimethyl ester

Conditions

Conditions	Yield
In toluene for 1h; Heating; Yield given;	A n/a B 87%
In toluene for 1h; Heating; Yields of byproduct given;	A n/a B 87%

...Expand

: 13200-60-7
Sarcosine ethyl ester

: 107819-90-9
1,3-bis(tert-butoxycarbonyl)-2-methyl-2-thiopseudourea

: N1,N2-bis(tert-butoxycarbonyl)-N3-methylguanidino-N3-acetic acid ethyl ester

Conditions

Conditions	Yield
With triethylamine; mercury dichloride In N,N-dimethyl-formamide at 20℃; for 4h;	87%

: 13200-60-7
Sarcosine ethyl ester

: 33166-79-9
ethyl m-toluoylacetate

: 1-methyl-3-(α-hydroxy-3'-methylbenzylidene)pyrrolidine-2,4-dione

Conditions

Conditions	Yield
Stage #1: Sarcosine ethyl ester; ethyl m-toluoylacetate In xylene at 125 - 130℃; for 20h; Stage #2: With sodium methylate In methanol; xylene at 20℃; for 48h;	86.5%

: 5-((9H-carbazol-4yl)oxy)pentanoic acid

: 13200-60-7
Sarcosine ethyl ester

: ethyl2-(5-((9H-carbazol-4yl)oxy)-N-methylpentanamido)acetate

Conditions

Conditions	Yield
With benzotriazol-1-ol; 1,2-dichloro-ethane; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 0 - 25℃; for 12h;	86.2%

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Synthetic route

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