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180570-71-2

180570-71-2 Structure

180570-71-2 Structure
IdentificationMore
[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 PropertiesBack 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
[Major Application]

peptide synthesis
[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)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

29242990
[Storage Class]

11 - Combustible Solids
Hazard InformationBack 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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