Fmoc-Asp-OH

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Names

[ CAS No. ]:
119062-05-4

[ Name ]:
Fmoc-Asp-OH

[Synonym ]:
Fmoc-Asp-OH
L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartic acid
N-Fmoc-L-aspartic acid
MFCD00237654
(2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}succinic acid
Fmoc-L-aspartic acid

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
587.2±45.0 °C at 760 mmHg

[ Molecular Formula ]:
C19H17NO6

[ Molecular Weight ]:
355.341

[ Flash Point ]:
308.9±28.7 °C

[ Exact Mass ]:
355.105591

[ PSA ]:
112.93000

[ LogP ]:
3.55

[ Vapour Pressure ]:
0.0±1.7 mmHg at 25°C

[ Index of Refraction ]:
1.628

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

[ Hazard Codes ]:
Xn

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Articles

Synthesis of N-linked glycopeptides via solid-phase aspartylation.

Org. Biomol. Chem. 8 , 3723-3733, (2010)

An efficient strategy for the preparation of N-linked glycopeptides is described. The method relies on the use of side chain protecting groups on aspartic acid residues, namely the allyl and Dmab este...

The aspartimide problem in Fmoc-based SPPS. Part I.

J. Pept. Sci. 9 , 36-46, (2003)

A variety of Asp beta-carboxy protecting groups, Hmb backbone protection and a range of Fmoc cleavage protocols have been employed in syntheses of the model hexapeptide H-VKDGYI-OH to investigate the ...

The aspartimide problem in Fmoc-based SPPS. Part II.

J. Pept. Sci. 9 , 518-526, (2003)

The sequence dependence of base-catalysed aspartmide formation during Fmoc-based SPPS was systematically studied employing the peptide models H-Val-Lys-Asp-Xaa-Tyr-Ile-OH. The extent of formation of a...


More Articles

Related Compounds

  • fmoc-asp-oh-15n
  • Fmoc-Asp-OH-1-13C
  • Fmoc-Asp-OH-2-13C
  • Fmoc-Asp(Ompe)-OH
  • Fmoc-Asp(CSY)-OH
  • FMOC-ASP(OTBU)-OH
  • Methyl 2-amino-2-[1-(3,4-difluorophenyl)cyclopropyl]acetate
  • tert-butyl N-[2-(4,5-difluoro-2-nitrophenyl)-1-oxopropan-2-yl]-N-methylcarbamate
  • Sodium5-(2-bromo-4-chlorophenyl)-1,3,4-thiadiazole-2-carboxylate
  • 5-(2-Bromo-4-chlorophenyl)-1,3,4-thiadiazole-2-carboxylic acid
  • 3-(aminomethyl)-3-(1-methyl-1H-pyrazol-3-yl)cyclobutan-1-ol
  • (1S)-1-(2-chloro-4,6-dimethylpyridin-3-yl)-2,2,2-trifluoroethan-1-ol
  • 5-Bromo-3-[(7-chloroisoquinolin-5-yl)methoxy]pyridine-2-carbaldehyde
  • {1-[(1S,5S)-6,6-dimethylbicyclo[3.1.1]heptan-2-yl]cyclobutyl}methanol
  • tert-butyl N-{1-[(3-bromophenyl)methyl]-1H-1,2,4-triazol-3-yl}carbamate
  • 2-(4,5,6,7-tetrahydro-1H-indol-2-yl)prop-2-en-1-amine
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