N-Boc-L-homoserine Methyl Ester

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Products Intro: Product Name:methyl (2S)-4-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoate
CAS:120042-11-7
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
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Products Intro: Product Name:N-Boc-L-Homoserine Methyl Ester
CAS:120042-11-7
Purity:>95% Package:0.1g;0.25g;1g;5g;10g;25g
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Products Intro: Product Name:(S)-Methyl 2-((tert-butoxycarbonyl)amino)-4-hydroxybutanoate
CAS:120042-11-7
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-64251
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Products Intro: Product Name:N-Boc-L-Homoserine Methyl Ester
CAS:120042-11-7
Purity:0.99 Package:1kg,5kg,25kgs,200kgs;bulk
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Products Intro: Product Name:(S)-Methyl 2-((tert-butoxycarbonyl)amino)-4-hydroxybutanoate
CAS:120042-11-7
Purity:0.98 Package:5KG;1KG,grace@coreychem.com
N-Boc-L-homoserine Methyl Ester Basic information
Product Name:N-Boc-L-homoserine Methyl Ester
Synonyms:methyl (2S)-4-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoate;N-[(1,1-Dimethylethoxy)carbonyl]-L-homoserine Methyl Ester;N-Boc-L-homoserine Methyl Ester;(S)-2-(tert-Butoxycarbonylamino)-4-hydroxybutyric Acid Methyl Este;methyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-4-hydroxybutanoate;L-Homoserine, N-[(1,1-dimethylethoxy)carbonyl]-, methyl ester;tert-butyl (S)-1-(methoxycarbonyl)-3-hydroxypropylcarbamate;Boc-L-Homoserine methyl ester
CAS:120042-11-7
MF:C10H19NO5
MW:233.26
EINECS:
Product Categories:
Mol File:120042-11-7.mol
N-Boc-L-homoserine Methyl Ester Structure
N-Boc-L-homoserine Methyl Ester Chemical Properties
Boiling point 364.6±37.0 °C(Predicted)
density 1.125±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Store in freezer, under -20°C
pka10.91±0.46(Predicted)
AppearanceColorless to light yellow Viscous Liquid
Safety Information
MSDS Information
N-Boc-L-homoserine Methyl Ester Usage And Synthesis
Synthesis
N-Boc-L-Homoserine

41088-86-2

Iodomethane

74-88-4

N-Boc-L-homoserine Methyl Ester

120042-11-7

To a solution of (S)-2-(tert-butoxycarbonylamino)-4-hydroxybutyric acid 206 (8.5 g, 38 mmol) in DMF (50 mL) was added K2CO3 (5.24 g, 38 mmol) and iodomethane (5.4 g, 38 mmol). The reaction mixture was stirred at room temperature overnight. After the reaction was completed, the reaction mixture was diluted with water (500 mL) and extracted with dichloromethane (500 mL). The organic layers were combined, dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure to remove the solvent to afford the crude product (S)-2-((tert-butoxycarbonyl)amino)-4-hydroxybutyric acid methyl ester 207 (8.5 g, 90% yield).

References[1] Patent: WO2017/189866, 2017, A1. Location in patent: Paragraph 0243
[2] Patent: WO2017/156074, 2017, A1. Location in patent: Paragraph 00494
[3] Biochemistry, 2017, vol. 56, # 8, p. 1062 - 1074
[4] Patent: WO2016/112088, 2016, A1. Location in patent: Paragraph 0481
N-Boc-L-homoserine Methyl Ester Preparation Products And Raw materials
Raw materialsN-Boc-L-Homoserine-->Di-tert-butyl dicarbonate-->L-Homoserine-->L-homoserine methyl ester-->Iodomethane-->N,N-Dimethylformamide-->Potassium carbonate
Tag:N-Boc-L-homoserine Methyl Ester(120042-11-7) Related Product Information
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