47695

Fmoc-Cys(Trt)-OH

≥95.0% (sum of enantiomers, HPLC)

Manufacturer: Sigma Aldrich

CAS Number: 103213-32-7

Synonym(S): N-(9-Fluorenylmethoxycarbonyl)-S-trityl-L-cysteine, Nα-Fmoc-S-trityl-L-cysteine

Select a Size

Pack Size SKU Availability Price
5 G 47695-5-G In Stock ₹ 7,122.85
100 G 47695-100-G In Stock ₹ 17,763.83
1 KG 47695-1-KG In Stock ₹ 92,651.18

47695 - 5 G

₹ 7,122.85

In Stock

Quantity

1

Base Price: ₹ 7,122.85

GST (18%): ₹ 1,282.113

Total Price: ₹ 8,404.963

Quality Level

100

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

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Description

  • General description: Fmoc-Cys(Trt)-OH is an amino acid commonly used in the Fmoc solid-phase peptide synthesis. [1]
  • Application: Fmoc-Cys(Trt)-OH is an N-terminal protected cysteine derivative used in peptide synthesis. Some of the examples are:Synthesis of mono- and bi-functionalized platinum(IV) complexes to target angiogenic tumor vasculature.[2]Synthesis of proteins through native chemical ligation of peptide hydrazides as thioester surrogates via solid-phase synthesis.[3]Synthesis of glycoconjugates by conjugating reducing sugars to cysteine residues of peptides.[4]

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves