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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inquiryHebei yanxi chemical co., LTD is a professional research, development and production 2-phenylacetamide enterprise backbone members by local well-known entrepreneurs and professional senior engineers in the party's "low carbon environ
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
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inquiryAppearance:White to off white crystalline powder Storage:ln stock Package:25kg/Barrel Application:Chemicals Transportation:Express/Sea/Air Port:Any port of china
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inquiryTIANFUCHEM--79416-27-6--High purity 5-Aminolevulinic acid methyl ester hydrochloride factory price Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China An
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Cas:79416-27-6
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inquiry5-Aminolevulinic acid methyl ester hydrochloride CAS:79416-27-6 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing
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inquiryPacking: According to customer requirements Delivery time: In stock or depands Port of shipment: Ningbo/Shanghai/Qingdao OEM/ODM:Welcome Sample:We can offer our existing samples at once Transportation:Express/Sea/Air Port:Ningbo/Shanghai/Qingd
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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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inquiryZibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
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inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
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inquiryZhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed
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inquiryLocated in Hangzhou National Hi-Tech Industrial Development Zone, zhongqichem is a technical company mainly focus on the Custom synthesis, manufacturing, sales of chemicals to various industries. Benefiting from the outstanding customer service and h
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inquiryHigh 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:Active Pharmaceutical I
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inquiryLower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
Conditions | Yield |
---|---|
With thionyl chloride at 20℃; for 30h; | 86.3% |
With thionyl chloride at 20℃; for 48h; | 81% |
With thionyl chloride at 0 - 20℃; | |
With thionyl chloride |
Conditions | Yield |
---|---|
With thionyl chloride at 60℃; for 5h; |
methyl 5-bromo-4-oxopentanoate
methyl aminolevulinate
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 1.) K2CO3 / 1.) DMFA, 20 deg C, 20 min, 2.) 72 h, 3.) water, 20 deg C, 24 h 2: 1.) conc. HCl, 2.) conc. HCl / 1.) water, reflux, 10 h, 2.) acetone, 60-70 deg C 3: 81 percent / SOCl2 / 48 h / 20 °C View Scheme |
methyl 5-(1,3-dioxoisoindolin-2-yl)-4-oxopentanoate
methyl aminolevulinate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) conc. HCl, 2.) conc. HCl / 1.) water, reflux, 10 h, 2.) acetone, 60-70 deg C 2: 81 percent / SOCl2 / 48 h / 20 °C View Scheme |
levulinic acid
methyl aminolevulinate
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 10.7 g / Br2, urea / 48 h / 20 °C 2: 1.) K2CO3 / 1.) DMFA, 20 deg C, 20 min, 2.) 72 h, 3.) water, 20 deg C, 24 h 3: 1.) conc. HCl, 2.) conc. HCl / 1.) water, reflux, 10 h, 2.) acetone, 60-70 deg C 4: 81 percent / SOCl2 / 48 h / 20 °C View Scheme |
2,2-dimethyl-4,6-dioxo-5-(3-phthalimido-2-oxopropyl)-1,3-dioxane
methyl aminolevulinate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) conc. HCl, 2.) conc. HCl / 1.) water, reflux, 10 h, 2.) acetone, 60-70 deg C 2: 81 percent / SOCl2 / 48 h / 20 °C View Scheme |
5-aminolevulinic acid hydrochloride
methyl aminolevulinate
Conditions | Yield |
---|---|
With hydrogenchloride In methanol | |
With hydrogenchloride In methanol |
methyl aminolevulinate
(2S,4S)-1-(tert-butoxycarbonyl)-4-fluoropyrrolidine-2-carboxylic acid
5-[(1-tert-butoxycarbonyl-(4S)-fluoro-(2S)-pyrrolidinyl)carbonylamino]levulinic acid methyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; | 100% |
methyl aminolevulinate
(2S,4R)-1-(tert-butoxycarbonyl)-4-methoxypyrrolidine-2-carboxylic acid
5-[(1-tert-butoxycarbonyl-(4R)-methoxy-(2S)-pyrrolidinyl)carbonylamino]levulinic acid methyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; | 100% |
1-(tert-butoxycarbonyl)-L-proline
methyl aminolevulinate
N-(N-tert-butoxycarbonyl-L-prolyl)-5-aminolaevulinic acid methyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; | 100% |
methyl aminolevulinate
(2S,3aS,7aS)-1-(tert-butoxycarbonyl)octahydro-1H-indole-2-carboxylic acid
5-[(1-tert-butoxycarbonyl-(2S)-octahydroindolyl)carbonylamino]levulinic acid methyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1,2-dichloro-ethane; triethylamine In dichloromethane; water | 100% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; | 100% |
(1-tert-butoxycarbonyl-(4S)-isopropoxy-(2S)-pyrrolidinyl)carboxylic acid
methyl aminolevulinate
5-[(1-tert-butoxycarbonyl-(4S)-isopropoxy-(2S)-pyrrolidinyl)carbonylamino]levulinic acid methyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; | 100% |
(1-tert-butoxycarbonyl-(4S)-cyclobutoxy-(2S)-pyrrolidinyl)carboxylic acid
methyl aminolevulinate
5-[(1-tert-butoxycarbonyl-(4S)-isopropoxy-(2S)-pyrrolidinyl)carbonylamino]levulinic acid methyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; | 100% |
methyl aminolevulinate
(2S,4R)-4-acetoxy-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid
5-[(4R)-acetoxy-1-tert-butoxycarbonyl-(2S)-pyrrolidinylcarbonylamino]levulinic acid methyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; | 100% |
methyl aminolevulinate
5-[(1-tert-butoxycarbonyl-(5S)-methoxymethyl-(2S)-pyrrolidinyl)carbonylamino]levulinic acid methyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; | 100% |
methyl aminolevulinate
(2S,4S)-1-[(tert-butoxy)carbonyl]-4-methoxypyrrolidine-2-carboxylic acid
5-[(1-tert-butoxycarbonyl-(4S)-methoxy-(2S)-pyrrolidinyl)carbonylamino]levulinic acid methyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; | 99% |
t-butyloxycarbonyl-O-benzyl-L-tyrosine hydroxysuccinimide ester
methyl aminolevulinate
N-(N(α)-tert-butoxycarbonyl-O-(benzyl)-L-tyrosyl)-5-aminolaevulinic acid methyl ester
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 98% |
O1-(2,5-dioxopyrrolidin-1-yl)-O4-tert-butyl-(2S)-2-(tert-butoxycarbonylamino)-butanedioate
methyl aminolevulinate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 98% |
2,5-dioxopyrrolidin-1-yl N-(tert-butoxycarbonyl)-L-tryptophanate
methyl aminolevulinate
N-(N-tert-butoxycarbonyl-L-tryptophyl)-5-aminolaevulinic acid methyl ester
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 97% |
Conditions | Yield |
---|---|
Stage #1: pyropheophorbide a With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane for 2h; Stage #2: methyl aminolevulinate With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 6h; Inert atmosphere; | 96.1% |
succinimido (tert-butyloxycarbony) serinate
methyl aminolevulinate
N-(N-tert-butoxycarbonyl-L-seryl)-5-aminolaevulinic acid methyl ester
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 96% |
benzyl [(2S)-1-amino-1-oxo-3-phenylpropan-2-yl]carbamate
methyl aminolevulinate
Conditions | Yield |
---|---|
Stage #1: benzyl [(2S)-1-amino-1-oxo-3-phenylpropan-2-yl]carbamate; methyl aminolevulinate With benzotriazol-1-ol; 1-n-butyl-3-methylimidazolim bromide; dicyclohexyl-carbodiimide In tetrahydrofuran at 20℃; for 2h; Inert atmosphere; Stage #2: With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 96% |
tertbutoxycarbonyl-L-methionine N-hydroxysuccinimide ester
methyl aminolevulinate
N-(N-tert-butoxycarbonyl-L-methionyl)-5-aminolaevulinic acid methyl ester
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 95% |
methyl aminolevulinate
Nα-Boc-D-tryptophan-N-hydroxysuccinimide ester
N-(N-tert-butoxycarbonyl-D-tryptophyl)-5-aminolaevulinic acid methyl ester
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 95% |
methyl aminolevulinate
Boc-Phe-ONSu
methyl 5-((2'-tert-butyloxycarbonylamino)-L-phenylpropionyl)amino-4-oxopentanoate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 95% |
methyl aminolevulinate
Conditions | Yield |
---|---|
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 6h; | 94.9% |
(S)-5-tert-butyl 1-(2,5-dioxopyrrolidin-1-yl) 2-((tert-butoxycarbonyl)amino)pentanedioate
methyl aminolevulinate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 94% |
tert-butoxycarbonyl-L-proline N-hydroxysuccinimide ester
methyl aminolevulinate
N-(N-tert-butoxycarbonyl-L-prolyl)-5-aminolaevulinic acid methyl ester
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 94% |
benzoyl chloride
methyl aminolevulinate
methyl 5-(N-benzoyl)amino-4-oxopentanoate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 3h; Inert atmosphere; | 94% |
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere; | 91% |
2-furancarbonyl chloride
methyl aminolevulinate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere; | 94% |
2-Thiophenecarbonyl chloride
methyl aminolevulinate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere; | 94% |
methyl aminolevulinate
5-[(1-tert-butoxycarbonyl-(5S)-ethoxymethyl-(2S)-pyrrolidinyl)carbonylamino]levulinic acid methyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; | 93% |
methyl aminolevulinate
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1,2-dichloro-ethane In water | 93% |
methyl aminolevulinate
δ-aminolevulinic acid methyl ester phosphate
Conditions | Yield |
---|---|
With phosphoric acid; triethylamine In water at 0 - 20℃; for 0.166667h; | 93% |
N-tertiarybutoxycarbonyl-D-alanine N-hydroxysuccinimide ester
methyl aminolevulinate
N-(N-tert-butoxycarbonyl-D-alanyl)-5-aminolaevulinic acid methyl ester
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 93% |
Boc-Lys(Z)-OSu
methyl aminolevulinate
N-(N(α)-tert-butoxycarbonyl-N(ε)-(benzyloxycarbonyl)-L-lysyl)-5-aminolaevulinic acid methyl ester
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 93% |
2,5-dioxopyrrolidin-1-yl N2-(((9H-fluoren-9-yl)methoxy)carbonyl)-N6-(tert-butoxycarbonyl)-L-lysinate
methyl aminolevulinate
N-(N(α)-(9-fluorenylmethoxycarbonyl)-N(ε)-(tert-butoxycarbonyl)-L-lysyl)-5-aminolaevulinic acid methyl ester
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 93% |
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