| Identification | More | [Name]
N-(9-Fluorenylmethyloxycarbonyl)-N'-trityl-D-asparagine | [CAS]
180570-71-2 | [Synonyms]
FMOC-D-ASN(TRT)
FMOC-D-ASN(TRT)-OH
FMOC-D-ASPARAGINE(TRITYL)
FMOC-D-ASPARAGINE(TRT)
FMOC-N-BETA-TRITYL-D-ASPARAGINE
FMOC-N-GAMMA-TRITYL-D-ASPARAGINE
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-BETA-TRITYL-D-ASPARAGINE
N-ALPHA-9-FLUORENYLMETHOXYCARBONYL-N-OMEGA-TRITYL-D-ASPARAGINE
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-BETA-TRITYL-D-ASPARAGINE
N-ALPHA-FMOC-N-BETA-TRITYL-D-ASPARAGINE
N-(9-FLUORENYLMETHYLOXYCARBONYL)-N''-TRITYL-D-ASPARAGINE
NALPHA-9-Fluorenylmethoxycarbonyl-NB-trityl-D-asparagine
N-.ALPHA.-FMOC-N-.GAMMA.-TRITYL-D-ASPARAGINE
N-α-Fmoc-β-trityl-D-asparagine | [Molecular Formula]
C38H32N2O5 | [MDL Number]
MFCD00151919 | [Molecular Weight]
596.67 | [MOL File]
180570-71-2.mol |
| Chemical Properties | Back Directory | [Melting point ]
211-216°C | [Boiling point ]
858.1±65.0 °C(Predicted) | [density ]
1.271±0.06 g/cm3(Predicted) | [storage temp. ]
-20°C | [solubility ]
Acetonitrile (Slightly), Chloroform (Slightly), Methanol (Sparingly) | [form ]
Solid | [pka]
3.79±0.10(Predicted) | [color ]
White to Off-White | [Stability:]
Acid Sensitive | [InChIKey]
LEAIJCJTJSTEDG-UUWRZZSWSA-N | [SMILES]
C(O)(=O)[C@@H](CC(N)=O)N(C(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O)C(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1 | [CAS DataBase Reference]
180570-71-2(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Description]
Fmoc-D-Asn(Trt)-OH (180570-71-2) is the dextrorotary form of Asparagine, and its side chain is protected by Trt group. D-amino acids are toxic in a variety of animals. However, the study of D-amino acids will contribute to the development of new drugs. Fmoc is often preferred over Boc because of its ease of cleavage
| [Chemical Properties]
White powder | [Uses]
Fmoc-d-asn(trt)-oh, is an amino acid building block used in peptide synthesis. With a growing peptide drug market the fast, reliable synthesis of peptides is of great importance. | [reaction suitability]
reaction type: Fmoc solid-phase peptide synthesis |
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