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N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-D-lysine

N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-D-lysine structure

CAS No:
214750-75-1
Formula:
C25H28N2O6
Chemical Name:
N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-D-lysine
Synonyms:
D-Lysine,N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-;D-Lysine,N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propenyloxy)carbonyl]-;N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-D-lysine;Fmoc-D-Lys(Alloc);(2R)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-6-(prop-2-enoxycarbonylamino)hexanoic acid
Categories:
Biochemical Engineering > Amino Acids and Derivatives

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Description

White powder

N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-D-lysine Basic Attributes

Molecular Weight：

452.5

Exact Mass：

452.50

HScode：

2924299090

Characteristics

PSA：

114

XLogP3：

4.1

Appearance：

White Powder

Density：

1.2±0.1 g/cm3

Boiling Point：

689.7°C at 760 mmHg

Flash Point：

370.9±31.5 °C

Refractive Index：

1.579

Storage Conditions：

2-8°C

Safety Information

Transport codes：

NONH for all modes of transport

wgk germany：

N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-D-lysine Use and Manufacturing

(0042) FIG. 2 depicts a synthesis of Pt-LHRH conjugate in accordance with a preferred embodiment of the present invention. The Mal-LHRH decapeptide was synthesized using Fmoc solid phase chemistry techniques and then chelated to activated cisplatin. Fmoc-Rink Amide-AM resin was placed onto a reaction vessel and washed with DMF and DCM in continuous-flow mode using a PS3 peptide synthesizer. The side chain protected amino acids derivatives used were Fmoc-Gly-OH, Fmoc-Pro-OH, Fmoc-Arg(Pbf)-OH, Fmoc-Leu-OH, LHRH-curcumin conjugate was synthesized by Fmoc solid phase chemistry techniques. H-Rink Amide ChemMatrix resin (0.52 mmol) was placed into a column. The resin was then washed with DMF in continuous-flow mode using a Pioneer Peptide Synthesizer. The side chain-protected amino acid derivatives used were, in sequence, Fmoc-Glu(OtBu)-OH, Fmoc-His(Trt)-OH, Fmoc-Trp(Boc)-OH, Fmoc-Ser(tBu)-OH, Fmoc-Tyr(tBu)-OH,

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N-Fmoc-N-allyloxycarbonyl-D-lysine

CAS No.: 214750-75-1

Content: 99.00%

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Guide of N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-D-lysine

Description
Basic Attributes
Characteristics
Safety Information
Use and Manufacturing
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N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-D-lysine

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