N-boc Asp(OH)Ome

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N-boc Asp(OH)Ome manufacturers

  • Boc-L-Asp-Ome
  • Boc-L-Asp-Ome pictures
  • 2026-09-15
  • CAS:98045-03-5
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1T+
  • N-boc Asp(OH)Ome
  • N-boc Asp(OH)Ome pictures
  • $1.00
  • 2020-01-05
  • CAS:98045-03-5
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 100KG
N-boc Asp(OH)Ome Basic information
Product Name:N-boc Asp(OH)Ome
Synonyms:N-Boc-L-aspartic acid 1-Methyl ester, 98%;N-boc Asp(OH)Ome;N-[(1,1-Dimethylethoxy)carbonyl]-L-aspartic acid alpha-methyl ester;N-tert-Butoxycarbonyl-L-aspartic acid 1-methyl ester;1-Methyl N-(tert-Butoxycarbonyl)-L-aspartate;(Tert-Butoxy)Carbonyl Asp-OMe;N-tert-Butoxycarbonyla spartic acid a-methylester;α-methyl N-(tert-butoxycarbonyl)aspartate
CAS:98045-03-5
MF:C10H17NO6
MW:247.25
EINECS:
Product Categories:
Mol File:98045-03-5.mol
N-boc Asp(OH)Ome Structure
N-boc Asp(OH)Ome Chemical Properties
Melting point 79-81℃
Boiling point 407.1±40.0 °C(Predicted)
density 1.209
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka4.09±0.19(Predicted)
form Solid
color White to Almost white
Safety Information
HS Code 2924.19.8000
MSDS Information
N-boc Asp(OH)Ome Usage And Synthesis
UsesN-Boc-L-aspartic acid 1-methyl ester is used as an intermediate in the preparation of modified alfa-amino acids and 5-cis-alkylprolines.
Synthesis
L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-methyl4-(phenylmethyl) ester

80963-12-8

N-boc Asp(OH)Ome

98045-03-5

Boc-L-aspartyl (OBn)(OMe)14 (5.88 g, 17.43 mmol) was dissolved in methanol (20 mL) in a 50 mL round-bottomed flask and 10% palladium carbon catalyst was added under nitrogen protection. The reaction system was replaced three times with nitrogen and then three times with hydrogen. Subsequently, the reaction mixture was stirred under hydrogen atmosphere and atmospheric pressure for 6 hours. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated to afford the target product (S)-3-((tert-butoxycarbonyl)amino)-4-methoxy-4-oxobutanoic acid (Compound 15) in the form of a colorless gel (4.1 g, 95% yield). The specific optical rotation [α]21D of the product was 34 (c 0.1, CHCl3).1H NMR (CDCl3, 400 MHz) δ: 1.43 (s, 9H), 2.83-2.86 (d, 1H, J = 16.92 Hz), 3.01-3.05 (d, 1H, J = 16.68 Hz), 3.74 (s, 3H), 4.57 (s , 1H), 5.55-5.57 (d, 1H, J = 8.12 Hz), 10.45 (s, 1H).13C NMR (CDCl3, 100 MHz) δ: 28.3, 36.6, 49.7, 52.8, 80.5, 155.5, 171.5, 176.0. IR (KBr) ν: 3366, 2980, 1719 , 1506, 1440, 1395, 1368, 1222, 1165, 1060, 1008, 864, 764, 587 cm-1.

References[1] Organic and Biomolecular Chemistry, 2007, vol. 5, # 9, p. 1459 - 1465
[2] Tetrahedron Letters, 2014, vol. 55, # 14, p. 2274 - 2276
[3] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 1, p. 15 - 20
[4] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 2, p. 586 - 590
[5] Carbohydrate Research, 2013, vol. 382, p. 36 - 42
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