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Boc-D-Asparagine

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Boc-D-Asparagine Basic information

Product Name:
Boc-D-Asparagine
Synonyms:
  • NALPHA-BOC-D-ASPARAGINE
  • N-BOC-D-ASPARAGINE
  • NALPHA-(TERT-BUTOXYCARBONYL)-D-ASPARAGIN
  • NALPHA-(TERT-BUTOXYCARBONYL)-D-ASPARAGINE
  • N-ALPHA-TERT-BUTYLOXYCARBONYL-D-ASPARAGINE
  • N-ALPHA-T-BUTYLOXYCARBONYL-D-ASPARAGINE
  • N-ALPHA-T-BUTOXYCARBONYL-D-ASPARAGINE
  • N-ALPHA-T-BOC-D-ASPARAGINE
CAS:
75647-01-7
MF:
C9H16N2O5
MW:
232.23
EINECS:
231-405-2
Product Categories:
  • Asparagine [Asn, N]
  • Amino Acids (N-Protected)
  • Biochemistry
  • Boc-Amino Acids
  • Amino Acids
  • Amino Acid Derivatives
Mol File:
75647-01-7.mol
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Boc-D-Asparagine Chemical Properties

Melting point:
165-169 °C
alpha 
9 º (c=1, DMF)
Boiling point:
374.39°C (rough estimate)
Density 
1.2896 (rough estimate)
refractive index 
7.7 ° (C=1, DMF)
storage temp. 
Sealed in dry,2-8°C
solubility 
soluble in Dimethylformamide
pka
3.79±0.10(Predicted)
form 
Powder
color 
White
BRN 
4843040
CAS DataBase Reference
75647-01-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
T
Risk Statements 
25
Safety Statements 
24/25-45
WGK Germany 
3
HS Code 
29241990

MSDS

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Boc-D-Asparagine Usage And Synthesis

Chemical Properties

white fine crystalline powder

Uses

Nα-Boc-D-asparagine is an N-Boc-protected form of D-Asparagine (A788990). D-Asparagine is an isomer of L-Asparagine (A790005) and is used by bacteria (such as Saccharomyces cerevisiae) as a sole nitrogen source for replication. L-Asparagine is also a competitive inhibitor of staphylococcal L-asparaginase and is used as a reagent to synthesize peptide antibiotics.

Definition

ChEBI: Boc-D-asparagine is an asparagine derivative.

reaction suitability

reaction type: Boc solid-phase peptide synthesis

Synthesis

2058-58-4

24424-99-5

7536-55-2

General procedure for the synthesis of BOC-L-asparagine from D-asparagine monohydrate and di-tert-butyl dicarbonate: in Example 75, 5-[5-fluoro-2-oxo-1,2-dihydro-indol-(3Z)-ylidene-methylene]-2,4-dimethyl-1H-pyrrole-3-carboxylic acid [(S)-1-(2-methoxy-ethyl)-2,5-dioxo-pyrrolidin- 3-yl]-amide ester (75a, 2.0 g, 15 mmol) and Na2CO3 (1.6 g, 15 mmol) were dissolved in a solvent mixture of H2O/1,4-dioxane (30 mL/30 mL). To this solution, di-tert-butyl dicarbonate (Boc)2O (3.96 g, 18.2 mmol) was added dropwise at room temperature. The reaction mixture was stirred overnight and subsequently 1,4-dioxane was removed by evaporation. The remaining aqueous solution was adjusted to pH=2 with 37% HCl. The precipitate precipitated was filtered, washed with water and dried to afford the target product 75b (2.97 g, 84% yield) as a white solid.

References

[1] Patent: WO2008/33562, 2008, A2. Location in patent: Page/Page column 86
[2] Patent: US2009/76005, 2009, A1. Location in patent: Page/Page column 44
[3] Journal of Medicinal Chemistry, 2013, vol. 56, # 7, p. 2936 - 2947
[4] Journal of the American Chemical Society, 2014, vol. 136, # 26, p. 9244 - 9247

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