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Available Variants1 g
CHA.89111-1g
Price
€245.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.89111-1g | €245.60 |
≥97% (HPLC)
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C25H20F3NO4 |
|---|---|
| CAS Number | 247113-86-6 |
| Molecular Weight | 455.43 |
| NACRES | NA.26 |
| PubChem Substance ID | 57651130 |
| UNSPSC Code | 12352209 |
| MDL number | MFCD00797581 |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves, type N95 (US) |
Technical Overview & Applications Use-case context
Fmoc-Phe(4-CF3)-OH, also known by its CAS number 247113-86-6, is a non-natural amino acid derivative commonly utilized in peptide synthesis. The incorporation of this compound into peptides can significantly influence their physical and chemical properties, such as hydrophobicity and stability. The presence of the trifluoromethyl group at the 4-position of the phenyl ring in Fmoc-Phe(4-CF3)-OH imparts unique characteristics to the resulting peptides, which can be advantageous in various biomedical and pharmaceutical applications. This amino acid derivative is typically employed in solid-phase peptide synthesis, where the Fmoc protecting group facilitates the sequential addition of amino acids to form the desired peptide sequence. The use of Fmoc-Phe(4-CF3)-OH enables the creation of peptides with distinct properties, which can be exploited to develop novel therapeutic agents or probes for biological studies.
