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64905-10-8

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64905-10-8 Structure

64905-10-8 Structure
IdentificationBack Directory
[Name]

BOC-D-TRP(FOR)-OH
[CAS]

64905-10-8
[Synonyms]

BOC-D-TRP(CHO)
BOC-D-TRP(CHO)-OH
BOC-D-TRP(FOR)-OH
Boc-D-Trp(Boc)-OH
BOC-D-TRP(FORMYL)-OH
BOC-D-TRYPTOPHAN(FOR)-OH
BOC-D-(FORMYL)-TRYPTOPHAN
BOC-D-TRP(FOR)-OH USP/EP/BP
BOC-NIN-FORMYL-D-TRYPTOPHAN
Boc-D-Trp(Formyl)-OH.solvent
BOC-D-TRYPTOPHAN(NIN-FORMYL)
Nα-Boc-Nin-formyl-D-tryptophan
N-α-Boc-N-in-formyl-D-tryptophan
N-ALPHA-T-BOC-N-FORMYL-D-TRYPTOPHAN
N-ALPHA-BOC-NIN-FORMYL-D-TRYPTOPHAN
(Tert-Butoxy)Carbonyl D-Trp(For)-OH
N-ALPHA-T-BOC-N-IN-FORMYL-D-TRYPTOPHAN
N-ALPHA-T-BUTYLOXYCARBONYL-N'-FORMYL-D-TRYPTOPHANE
Boc-D-Trp(For)-OH N-α-Boc-N-in-forMyl-D-tryptophan
N-ALPHA-T-BUTYLOXYCARBONYL-N-IN-FORMYL-D-TRYPTOPHAN
NALPHA-tert-Butoxycarbonyl-Nin-formyl-D-tryptophane
N-ALPHA-TERT-BUTYLOXYCARBONYL-N'-FORMYL-D-TRYPTOPHANE
N-[(1,1-Dimethylethoxy)carbonyl]-1-formyl-D-tryptophan
D-Tryptophan,N-[(1,1-dimethylethoxy)carbonyl]-1-formyl-
Na-Boc-Nin-formyl-D-tryptophan≥ 99% (assay by titration)
(R)-2-((tert-Butoxycarbonyl)amino)-3-(1-formyl-1H-indol-3-yl)propanoic acid
(2R)-2-{[(tert-butoxy)carbonyl]amino}-3-(1-formyl-1H-indol-3-yl)propanoic acid
(2R)-3-(1-formylindol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoicaci
(2R)-3-(1-formylindol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
[Molecular Formula]

C17H20N2O5
[MDL Number]

MFCD00038004
[MOL File]

64905-10-8.mol
[Molecular Weight]

332.35
Chemical PropertiesBack Directory
[density ]

1.26±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[pka]

3.82±0.10(Predicted)
[Sequence]

Boc-{d-Trp(For)}
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H315-H314
[Precautionary statements ]

P260-P264-P270-P280-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P310-P332+P313-P362-P405-P501
Hazard InformationBack Directory
[Uses]

Boc-D-Thr(Bzl)-OH, is an amino acid derivative that can be used in the synthesis of millepachine amino acid prodrugs with enhanced solubility as antitumor agents.
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