47695
Fmoc-Cys(Trt)-OH
≥95.0% (sum of enantiomers, HPLC)
Synonym(s):
N-(9-Fluorenylmethoxycarbonyl)-S-trityl-L-cysteine, Nα-Fmoc-S-trityl-L-cysteine
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About This Item
Quality Level
assay
≥95.0% (sum of enantiomers, HPLC)
optical activity
[α]20/D +16.0±2°, c = 1% in THF
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
mp
170-173 °C (lit.)
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
SMILES string
OC(=O)[C@H](CSC(c1ccccc1)(c2ccccc2)c3ccccc3)NC(=O)OCC4c5ccccc5-c6ccccc46
InChI
1S/C37H31NO4S/c39-35(40)34(38-36(41)42-24-33-31-22-12-10-20-29(31)30-21-11-13-23-32(30)33)25-43-37(26-14-4-1-5-15-26,27-16-6-2-7-17-27)28-18-8-3-9-19-28/h1-23,33-34H,24-25H2,(H,38,41)(H,39,40)/t34-/m0/s1
InChI key
KLBPUVPNPAJWHZ-UMSFTDKQSA-N
General description
Application
- Synthesis of mono- and bi-functionalized platinum(IV) complexes to target angiogenic tumor vasculature.
- Synthesis of proteins through native chemical ligation of peptide hydrazides as thioester surrogates via solid-phase synthesis.
- Synthesis of glycoconjugates by conjugating reducing sugars to cysteine residues of peptides.
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Global Trade Item Number
| SKU | GTIN |
|---|---|
| 47695-100G | 04061832372808 |
| 47695-1KG | 04061826222812 |
| 47695-5G | 04061832372822 |
| 47695-25G | 04061832372815 |