Fmoc-(2-indanyl)-Gly-OH
Fmoc-(2-indanyl)-Gly-OH (CAS: 205526-39-2), with the empirical formula C26H23NO4 and molecular weight 413.47 g/mol, is a protected unnatural amino acid derivative. It is a key building block utilized in peptide synthesis and chemical biology research. This compound serves as a valuable reagent for introducing specific structural modifications in peptides, advancing the development of novel therapeutic agents and biochemical probes.
- IUPAC
- Fmoc-(2-indanyl)-L-glycine
Peptide Synthesis
Fmoc-(2-indanyl)-Gly-OH is employed as a building block in solid-phase and solution-phase peptide synthesis. Its unique indanyl side chain allows for the construction of peptides with modified structures for research purposes.
Chemical Biology
This unnatural amino acid derivative is utilised in chemical biology to synthesise peptides with altered properties. These modified peptides can serve as probes for studying biological processes or as scaffolds for drug discovery.
Organic Synthesis
As a specialised reagent, Fmoc-(2-indanyl)-Gly-OH finds application in complex organic synthesis pathways. It enables the precise incorporation of its distinct structural motif into larger molecules.
| Molecular weight | 413.47 |
|---|---|
| Empirical formula | C26H23NO4 |
| Assay | ≥98.0% (HPLC) |
| Storage temperature | 2-8°C |
| Protective equipment | Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter |
|---|---|
| Water hazard class (WGK, DE) | 3 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Fmoc-(2-indanyl)-Gly-OH used for?
+
Fmoc-(2-indanyl)-Gly-OH is primarily used as a building block in peptide synthesis and chemical biology research, allowing for the creation of modified peptides with unique structural features.
What is the CAS number and empirical formula for Fmoc-(2-indanyl)-Gly-OH?
+
The CAS number is 205526-39-2, and the empirical formula is C26H23NO4.
What grade and purity does Tech Serve Solutions supply for Fmoc-(2-indanyl)-Gly-OH?
+
Tech Serve Solutions supplies Fmoc-(2-indanyl)-Gly-OH with an assay of ≥98.0% (HPLC). This compound is not supplied as USP, BP, EP, or pharmacopoeia grade.
What are the safety and handling recommendations for Fmoc-(2-indanyl)-Gly-OH?
+
Handling requires appropriate personal protective equipment, including eyeshields, gloves, and a type N95 (US) or type P1 (EN143) respirator filter. The compound has a WGK Germany rating of 3.
How is Fmoc-(2-indanyl)-Gly-OH typically packed and shipped by TSS?
+
This product is stored at 2-8°C. TSS is a global supplier and exporter, ensuring secure packaging and compliant shipping for chemical reagents.
How can I request a sample or quote for Fmoc-(2-indanyl)-Gly-OH?
+
To request a sample or obtain a quotation, please contact the Tech Serve Solutions sales team through our website or by direct inquiry.
▶ Related products
1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis
1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more
3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis
3-Methyl-1,5-pentanediol
Chemical Synthesis
3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis