DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:616-34-2
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inquiry1.In No Less 10 years exporting experience. you can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specializ
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Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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inquiryCangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new api
Cas:616-34-2
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
High quality,stable supply chain.Appearance:white/off-white or light yellow Storage:Store in cool and dry place, keep away from strong light and heat. Package:aluminum bottle,glass bottle,PTFE bottle,cardboard drum Application:This product can be use
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Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
Glycine, methyl esterAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:pharmaceutical intermediate Transportation:by air, by sea, by express
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
Cas:616-34-2
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United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innov
please contact us to confirm the required quantity and quote, we will provide you with COA,NMR,HPLC and other relevant informationAppearance:White or almost white crystalline powder Storage:Store in a cool place. Keep container tightly closed in a dr
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High Quality Best Price Storage:Store in dry, dark and ventilated place Application:Chemical Synthesis Intermediate
Debyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen
Produce in South China, less pressure in environment protection, more stable production.Honored as "National Hi-tech Enterprise" & "Shenzhen Hi-tech Enterprise";4000+m2 R&D center & 47,000m2 plant, 20 R&D technicians, tens of reactors from 100L to 50
Conditions | Yield |
---|---|
With chloro-trimethyl-silane at 0 - 4℃; for 24h; Inert atmosphere; | 100% |
With thionyl chloride at 0 - 65℃; for 4.25h; | 100% |
With thionyl chloride at 0 - 65℃; for 4.25h; | 100% |
N-(tert-butoxycarbonyl)glycine methyl ester
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
With trifluoroacetic acid In dichloromethane at 20℃; for 0.5h; Inert atmosphere; | 100% |
With methanol; tetradecanoyl chloride; sodium iodide In acetonitrile at 25℃; for 0.333333h; |
Conditions | Yield |
---|---|
With hydrogen for 0.583333h; | 98% |
With samarium; cobalt(II) chloride In tetrahydrofuran at 40℃; for 1h; Reduction; | 79% |
With samarium; nickel dichloride In tetrahydrofuran at 40℃; for 3h; | 76% |
Conditions | Yield |
---|---|
With ammonia In diethyl ether for 2h; | 90% |
With ammonia | 85% |
With anion exchange resin In dichloromethane for 0.0833333h; | 83% |
Conditions | Yield |
---|---|
With ammonium cerium(IV) nitrate Heating; | 80% |
Conditions | Yield |
---|---|
With samarium; iodine for 6h; Ambient temperature; | 74% |
L-tryptophan methyl ester
A
Indole-3-carboxaldehyde
B
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
With hydrogenchloride; pyrimido<5,4-g>pteridine N-oxide derivative In acetonitrile for 6h; Mechanism; Ambient temperature; Irradiation; analogeous reaction of 5 other tryptophan derivatives; | A 72% B n/a |
Conditions | Yield |
---|---|
With ammonia; water Erwaermen des Reaktionsprodukts mit methanol.HCl; das Hydrochlorid entsteht; | |
With ammonia; water Erwaermen des Reaktionsprodukts mit methanol.HCl; Gewinnung aus dem entstehenden Hydrochlorid mit Hilfe von Ag2O in wenig H2O enthaltendem Aether; |
Conditions | Yield |
---|---|
With trans- 2.) CH2Cl2, 0.2 M NBu4*BF4, electrolysis; Yield given. Multistep reaction; |
N-(2-methyl-3-oxoprop-1-enyl)glycine methyl ester
A
methylmalonaldehyde enol tautomer
B
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
With water Rate constant; Equilibrium constant; Ambient temperature; acetate buffer (pH 4.2); enaminal hydrolysis; stereochemistry and kinetics of formation of enaminals from reactions of malondialdehydes with various amino acids; |
((E)-3-Oxo-propenylamino)-acetic acid methyl ester
A
Malondialdehyde
B
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
With water Rate constant; Equilibrium constant; Ambient temperature; acetate buffer (pH 4.2); enaminal hydrolysis; stereochemistry and kinetics of formation of enaminals from reactions of malondiladehydes with various amino acids; |
Conditions | Yield |
---|---|
With ethanol das Hydrochlorid entsteht; |
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
With diethyl ether; ammonia at 0℃; Isolierung; | |
With sodium hydroxide; potassium carbonate at 0℃; Isolierung; |
hydrogenchloride
N-2-(2-hydroxyethylamino)-2-oxoethylbenzamide
A
Hippsaeure-(2-amino-ethyl)-ester
B
ethanolamine
C
methoxycarbonylmethylamine
1-methyl-4-nitrosobenzene
glycine ethyl ester hydrochloride
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
at 0℃; |
diethyl ether
glycine ethyl ester hydrochloride
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
at 0℃; |
Conditions | Yield |
---|---|
In tetrahydrofuran for 0.5h; |
Conditions | Yield |
---|---|
In methanol for 2h; Heating; |
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
With sodium hydroxide; glutaryl-7-aminocephalosporanic acid acylase In water at 25℃; pH=8.0; Enzyme kinetics; Enzymatic reaction; |
(dibenzylamino)acetic acid methyl ester
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen; 1-butyl-3-methylimidazolium Tetrafluoroborate In methanol at 20℃; under 760.051 Torr; for 12h; |
isocyanoacetic acid methyl ester
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
Stage #1: isocyanoacetic acid methyl ester In methanol; dichloromethane at 20℃; Stage #2: With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 2h; |
methyl (benzothiazole-2-sulfonyl)glycinate
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
With hydroxylamine; sodium hydroxide In water at 20℃; for 6h; pH=9 - 10; |
Conditions | Yield |
---|---|
With trifluoroacetic acid In dichloromethane |
Conditions | Yield |
---|---|
With trifluoroacetic acid In dichloromethane |
Conditions | Yield |
---|---|
With trifluoroacetic acid at 25℃; for 1h; |
Conditions | Yield |
---|---|
With trifluoroacetic acid |
Conditions | Yield |
---|---|
With triethylamine at 20℃; for 0.166667h; |
dimethyl (1,1-dimethyl-3-oxobutyl)phosphonate
potassium glycinate
B
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
In methanol Reflux; |
N-methylmaleimide
benzaldehyde
methoxycarbonylmethylamine
(1RS,3SR,3aRS,6aSR)-methyl 5-methyl-4,6-dioxo-3-phenyloctahydropyrrolo[3,4-c]pyrrole-1-carboxylate
Conditions | Yield |
---|---|
In toluene for 24h; Heating; | 100% |
N-methylmaleimide
phenylglyoxal hydrate
methoxycarbonylmethylamine
methyl (1S*,3R*,3aS*,6aR*)-3-benzoyl-5-methyl-4,6-dioxooctahydropyrrolo[3,4-c]pyrrole-1-carboxylate
Conditions | Yield |
---|---|
In chloroform for 16h; Heating; | 100% |
In chloroform for 16h; Heating; Yield given; |
2-allyl-2-hydroxycyclohexanone
methoxycarbonylmethylamine
[2-Allyl-2-hydroxy-cyclohex-(E)-ylideneamino]-acetic acid methyl ester
Conditions | Yield |
---|---|
In toluene Heating; | 100% |
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
With 4 A molecular sieve In dichloromethane at 20℃; for 2h; | 100% |
With molecular sieve Condensation; |
methoxycarbonylmethylamine
3-methoxy-1-(4-methoxy-phenyl)-4-oxo-azetidine-2-carbaldehyde
Conditions | Yield |
---|---|
With 4 A molecular sieve In dichloromethane at 20℃; for 2h; | 100% |
With molecular sieve Condensation; |
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
With 4 A molecular sieve | 100% |
With 4 A molecular sieve In dichloromethane at 20℃; for 2h; |
methoxycarbonylmethylamine
[pyrazol-1-yl-(toluene-4-sulfonylimino)-methyl]-carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 0.0833333h; | 100% |
2,4-Dimethoxybenzaldehyde
methoxycarbonylmethylamine
(2,4-dimethoxybenzylamino)acetic acid methyl ester
Conditions | Yield |
---|---|
With sodium tris(acetoxy)borohydride; triethylamine In 1,2-dichloro-ethane at 20℃; for 24h; | 100% |
Boc-Tyr(t-Bu)-OH
methoxycarbonylmethylamine
N-t-butoxycarbonyl-O-t-butyl-L-tyrosylglycine methyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; diisopropyl-carbodiimide In dichloromethane at 20℃; for 16h; | 100% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane | 95% |
adamantane-1,3-dicarboxylic acid
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide for 24h; | 100% |
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide for 24h; | 100% |
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 N,N-dimethyl-formamide at 20℃; for 8h; Inert atmosphere; | 100% |
methoxycarbonylmethylamine
methyl 2-(2-benzamido-2-(7-oxocyclohepta-1,3,5-trien-1-yl)propanamido)acetate
Conditions | Yield |
---|---|
In tetrahydrofuran at -20℃; | 100% |
With potassium carbonate In tetrahydrofuran at -20℃; | 100% |
Boc-D-Val-OH
methoxycarbonylmethylamine
((R)-2-tert-butoxycarbonylamino-3-methylbutyrylamino)-acetic acid methyl ester
Conditions | Yield |
---|---|
With 4-methyl-morpholine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate In dichloromethane at 5 - 20℃; | 100% |
formamide
methoxycarbonylmethylamine
methyl N-formylglycinate
Conditions | Yield |
---|---|
With Iron(III) nitrate nonahydrate In toluene for 24h; Reflux; | 100% |
Stage #1: formamide With bis(2-chlorophenyl)borinic acid; acetic acid at 45℃; for 0.25h; Sealed tube; Stage #2: methoxycarbonylmethylamine at 45℃; for 24h; Temperature; Sealed tube; | 99% |
methyl (2S)-2-amino-3-phenylpropanoate
methoxycarbonylmethylamine
(S)-PheGly
Conditions | Yield |
---|---|
Stage #1: methyl (2S)-2-amino-3-phenylpropanoate at 50℃; Ionic liquid; Inert atmosphere; Stage #2: With trifluoroacetic acid Stage #3: methoxycarbonylmethylamine Temperature; Further stages; | 99.9% |
Conditions | Yield |
---|---|
With thionyl chloride In methanol at -10℃; for 0.166667h; | 99.5% |
L-N-Boc-Ala
methoxycarbonylmethylamine
methyl 2-((2S)-2-((tert-butoxycarbonyl)amino)propanamido)acetate
Conditions | Yield |
---|---|
Stage #1: L-N-Boc-Ala With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 0.333333h; Inert atmosphere; Stage #2: methoxycarbonylmethylamine With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 9h; Inert atmosphere; | 99% |
With 4-methyl-morpholine; isobutyl chloroformate In tetrahydrofuran at -20 - 20℃; | 83% |
Stage #1: L-N-Boc-Ala With 4-methyl-morpholine In tetrahydrofuran; N,N-dimethyl-formamide at -15℃; Cooling with ethanol-dry ice; Stage #2: methoxycarbonylmethylamine With triethylamine; isobutyl chloroformate In tetrahydrofuran; N,N-dimethyl-formamide at 20℃; for 3h; Inert atmosphere; | 80% |
Conditions | Yield |
---|---|
In toluene Heating; | 99% |
With pyridine In dichloromethane; toluene at 0℃; for 2h; | |
With triethylamine In toluene |
m-methyl red
methoxycarbonylmethylamine
N-{3-[(N,N-dimethylaminophenyl)-4'-diazenyl]benzoyl}glycine methyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide | 99% |
Conditions | Yield |
---|---|
With triethylamine In ethyl acetate at 21℃; for 1h; Inert atmosphere; | 99% |
4-(2-methylquinolin-4-ylmethoxy)benzenesulfonyl chloride hydrochloride salt
methoxycarbonylmethylamine
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 0.5h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
Stage #1: 4-chlorobenzaldehyde; methoxycarbonylmethylamine With diisopropyl-carbodiimide In toluene for 3h; Inert atmosphere; Stage #2: Diethyl maleate With 2-(diphenylphosphino)-N-((S)-2-(((1S,2S)-2-(isobutylamino)-1,2-diphenylethyl)amino)-2-oxo-1-phenylethyl)benzamide; silver carbonate In toluene at 20℃; for 3h; Inert atmosphere; | 99% |
4-fluorobenzaldehyde
methoxycarbonylmethylamine
(4-fluorobenzylideneamino)acetic acid methyl ester
Conditions | Yield |
---|---|
In methanol at 60℃; for 0.5h; Microwave irradiation; | 99% |
Z-Leu-OH
methoxycarbonylmethylamine
methyl N-benzyloxycarbonyl-L-leucylglicynate
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃; Inert atmosphere; | 98% |
Boc-Lys(Z)-OH
methoxycarbonylmethylamine
Nα tert-Butyloxycarbonyl-Nε-carbobenzyloxy-L-lysyl-glycine methyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide | 98% |
(E)-2-Phenyl-3-pyrrolidin-1-yl-N-[1-pyrrolidin-1-yl-meth-(E)-ylidene]-thioacrylamide
methoxycarbonylmethylamine
(1,4-dihydro-5-phenyl-4-thioxopyrimidin-1-yl)essigsaeure-methylester
Conditions | Yield |
---|---|
In acetic acid for 0.0833333h; Heating; | 98% |
methoxycarbonylmethylamine
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-2-propen-1-yl-glycine
Conditions | Yield |
---|---|
With 4-methyl-morpholine; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate In N,N-dimethyl-formamide for 4h; Ambient temperature; | 98% |
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